2-Methoxy-4-vinylphenol

7786-61-0

4-vinylguaiacol

p-Vinylguaiacol

4-ETHENYL-2-METHOXYPHENOL

4-Hydroxy-3-methoxystyrene

Phenol, 4-ethenyl-2-methoxy-

o-methoxy-p-vinylphenol

para-vinylguaiacol

Guaiacol, 4-vinyl-

p-Vinyl guaiacol

4-vinyl-2-methoxyphenol

Phenol, 2-methoxy-4-vinyl-

4-Hydroxy-3-methoxyvinylbenzene

2-METHOXY-4-VINYL-PHENOL

FEMA No. 2675

3-Methoxy-4-hydroxystyrene

Varamol 106

CCRIS 548

CHEBI:42438

Vinylcatechol-O-methyl ether, P-

UNII-DA069CTH0O

EINECS 232-101-2

2M4VP

DA069CTH0O

Guaiacol, 4-vinyl

BRN 2044521

4-hydroxy-3-methoxyphenylethene

DTXSID7052529

2-(4-hydroxy-3-methoxyphenyl)ethene

2-Methoxy-4-ethenylphenol

Phenol, 2-methoxy-4-ethenyl

Phenol, 4-vinyl, 2-methoxy

CHEMBL1232595

DTXCID8031102

(4-Hydroxy-3-methoxyphenyl)ethene

3-06-00-04981 (Beilstein Handbook Reference)

4-vinyl guaiacol

EUG

Vinyl guaiacol

p-Vinyl guaicol

4-vinylguaiacole

4-Ethenylguaiacol

4-Vinyl-O-guaiacol

2-Methoxy-vinylphenol

31853-85-7

2-Metoxy-4-vinyl-phenol

bmse010071

4-ethenyl-2-methoxy-phenol

SCHEMBL54199

2-?Methoxy-?4-?vinylphenol

BCP27800

Tox21_304024

BDBM50548720

MFCD00015437

AKOS015890494

DB03514

FS-3782

HY-W019940

MCULE-4834642824

2-methoxy-4-vinylphenol (vinylguaiacol)

2-METHOXY-4-VINYLPHENOL [FHFI]

2-Methoxy-4-vinylphenol, >=98%, FG

NCGC00357234-01

Vinylguaiacol (4-vinyl-2-methoxyphenol)

BP-11167

PD006849

CAS-7786-61-0

2-Methoxy-4-vinylphenol (4-vinylguaiacol)

4-Vinyl-2-methoxyphenol (4-vinylguaiacol)

DB-003488

2-Methoxy-4-vinylphenol, analytical standard

4-Vinyl-2-methoxyphenol ( p-vinylguaiacol)

AM20041169

CS-0031749

NS00005168

C17883

EN300-1832370

A839253

Q4596898

W-104295

2-METHOXY-4-VINYLPHENOL (STABILIZED WITH TBC)

4M4

undecylenic acid

10-UNDECENOIC ACID

Undec-10-enoic acid

112-38-9

Undecenoic acid

Desenex

10-Hendecenoic acid

Renselin

Sevinon

Declid

10-Undecylenic acid

9-Undecylenic acid

Undecyl-10-enic acid

FEMA No. 3247

undecylenate

Kyselina undecylenova

Caswell No. 901

UNDECEN-10-ACID-1

Undecenoic acid, omega-

Undecylenic acid [JAN]

Hendecenoic acid, omega-

omega-undecenoic acid

NSC 2013

omega-hendecenoic acid

10-Henedecenoic acid

CHEBI:35045

undecelinic acid

10-Hendecenoic

10-Undecensaeure

NSC-2013

EINECS 203-965-8

n-Undecylenic acid

UNII-K3D86KJ24N

Undecen-10-saeure

Cruex

EPA Pesticide Chemical Code 085501

BRN 1762631

K3D86KJ24N

Cruex (TN)

Kyselina 9-decen-1-karboxylova

acide 10-undecylique

acido 10-undecenoico

1333-28-4

DTXSID8035001

acide 10-undecanoique

AI3-02065

NSC2013

MFCD00004442

Undecylenic acid (JAN/USP)

Undecylenic acid [USP:JAN]

DTXCID6015001

EC 203-965-8

4-02-00-01612 (Beilstein Handbook Reference)

Undesine

C11:1n-1

NCGC00159425-02

NCGC00159425-04

Undecylenic acid (USP:JAN)

UNDECYLENIC ACID (II)

UNDECYLENIC ACID [II]

UNDECENOIC ACID (MART.)

UNDECENOIC ACID [MART.]

Undecenoicacid

UNDECYLENIC ACID (USP-RS)

UNDECYLENIC ACID [USP-RS]

UNDECYLENIC ACID (EP MONOGRAPH)

UNDECYLENIC ACID [EP MONOGRAPH]

UNDECYLENIC ACID (USP MONOGRAPH)

UNDECYLENIC ACID [USP MONOGRAPH]

96451-28-4

CAS-112-38-9

Kyselina undecylenova [Czech]

10-Undecenoic acid, 98%

Kyselina 9-decen-1-karboxylova [Czech]

Desinex

Micocilen

Tobcharm

HongocuraM

HongocuraS

Antifungal Pen

undecylenic-acid

Remedy Nails

Anti-Fungal Pen

Rite Aid Fungal

Undecylenenic acid

MicocilenAntifungal

Topcare Antifungal

Antifungal Solution

Diabetic Antifungal

Anti-Fungal Liquid

Fungicure LiquidGel

10-Undecenic acid

Antifungal Nail Pen

EINECS 215-583-9

EmoniNail Antifungal

Hongocura Pinceladas

n-UNDECYLENIC ACID (10-1)

Zinc Undecylenate (undecylenic acid)

Anti-Fungal PenCVS

10-undeceneoic acid

Flexitol Anti Fungal

TERPENICOL

Zeta Clear Antifungal

NU CALMAR

HC Max Hongo CuraMS

Undecylenic Acid Liquid

Undecylenic acid, USAN

FungicureMaximum Strength

Premier Value Antifungal

FUNGWAY Fungus Clearing

Anti-Fungal Nail Solution

Good Neighbor Anti-Fungal

Tineacide Physician Formula

Fiore Rx Antifungal ProPen

Sally HansenNo More Fungus

Hongo KillerNail and Fungus

NCIOpen2_002642

UNDECYLENATE [VANDF]

WLN: QV9U1

Direct Naturals Fungus Clear

SCHEMBL17827

UNDECYLENIC ACID [MI]

Pinceladas Para Hongos Navarro

Maximum Strength Antifungal Pen

Diabetic Antifungal Professional

UNDECYLENIC ACID [INCI]

CHEMBL1276010

Myco Nail A Antifungal Solution

UNDECYLENIC ACID [VANDF]

FEMA 3247

Undecylenic acid, >=95%, FG

Undecylenic acid, >=96%, FG

TopCare AntifungalMaximum Strength

UNDECYLENIC ACID [WHO-DD]

HMS2093L21

Pharmakon1600-01505468

Fungicure Anti-Fungal Liquid 25%

Human Science Antifungal Foot Care

10-UNDECENOIC ACID [FHFI]

HY-B0914

PURESKIN FUNGAL NAIL RENEWAL

Tox21_111657

Tox21_300383

BBL027462

BDBM50248304

Fungi Nail Toe and Foot Anti-Fungal

LMFA01030036

NSC759153

Pinceladas Goyescas OriginalFungicide

s9452

STK801548

Dermaced Maximum Strength Anti-Fungal

FUNGINIX ANTI-FUNGAL TREATMENT

maximum strengthantifungal nail liquid

AKOS009031595

Tox21_111657_1

CCG-213461

DB11117

ELON Dual Defense Anti Fungal Formula

MCULE-7928135942

NSC-759153

PB48616

Undecylenic acid; Undec-10-enoic acid

10-Undecenoic acid, analytical standard

Premier Value AntifungalMaximum Strength

Botanimedix OnychoRX Antifungal Nail Gel

ETERNAL SPIRIT BEAUTY FUNGI FRESH

NCGC00159425-03

NCGC00159425-05

NCGC00159425-09

NCGC00254296-01

Undecylenic acid, natural, >=97%, FG

FLUSH Maximum Strength Antifungal formula

NCI60_001670

SBI-0206806.P001

SBI-0206806.P002

CVS Maximum Strength Anti-Fungal Pen 25%

Maximum Strength Antifungal Liquid Solution

Nutra Nail FUNGI FREE Antifungal Treatment

CVS PharmacyAnti-fungal Pen Maximum Strength

NS00009009

U0007

EN300-20666

Fiore Rx Coral Sorbet Antifungal Nail Polish

Pinceladas Goyescas OriginalBrush on Fungicide

10-Undecenoic acid, purum, >=97.0% (GC)

D02159

P19683

AB00630892_02

CVS MAXIMUM STRENGTH ANTI FUNGAL PEN 25

Fiore Rx CranApple Crush Antifungal Nail Polish

Fiore Rx Pixie Dust Pink Antifungal Nail Polish

Fiore Rx Antifungal Nail Lacquer Red Velvet Cake

Fiore Rx Rock Candy Clear Antifungal Nail Lacquer

Q420346

SR-05000002050

10-Undecenoic acid, Vetec(TM) reagent grade, 98%

Fiore Rx Almond Milk Matte Antifungal Nail Lacquer

Fiore Rx Eggplant My Garden Antifungal Nail Polish

Fiore Rx Pink Peppermint Pie Antifungal Nail Polish

RIte AidMaximum Strength Foot Care Anti-fungal Pen

SR-05000002050-1

W-200840

F0001-0258

Z104479700

CVS PharmacyMaximum Strength Antifungal Liquid with Aloe and Vitamin E

Undecylenic acid, United States Pharmacopeia (USP) Reference Standard

10-Undecenoic acid, puriss., meets analytical specification of Ph. Eur., BP, USP, 98-100.5%

InChI=1/C11H20O2/c1-2-3-4-5-6-7-8-9-10-11(12)13/h2H,1,3-10H2,(H,12,13

ETHYLENE

Ethene

Acetene

Elayl

Olefiant gas

74-85-1

Athylen

Etileno

9002-88-4

Bicarburretted hydrogen

Liquid ethylene

Ethylene, pure

Caswell No. 436

Aethylen

Aethen

HSDB 168

C2H4

EPA Pesticide Chemical Code 041901

Liquid ethyene

EINECS 200-815-3

CH2=CH2

H2C=CH2

Ethylene (8CI)

Ethylene, compressed

UNII-91GW059KN7

Ethene (9CI)

CHEBI:18153

91GW059KN7

CARBONEUM HYDROGENISATUM

DTXSID1026378

EC 200-815-3

MFCD00084423

UN 1038

UN 1962

Plastipore

ETHYLENE (IARC)

ETHYLENE [IARC]

ETHYLENE (II)

ETHYLENE [II]

R-1150

Athylen [German]

LDPE

Eteno

Ethylene [NF]

UN1038

UN1962

Ethene, 9CI

Ethylene-d3 (gas)

ETHYLENE-CMPD

ETHYLENE [HSDB]

ETHYLENE [MI]

Ethylene, 99.99%

ETHENE (ETHYLENE)

Heavy carburetted hydrogen

Ethylene, >=99.5%

Ethylene, >=99.9%

Ethylene, compressed [UN1962] [Flammable gas]

CHEMBL117822

DTXCID605931

Ethylene, purum, >=99.9%

DTXSID00949506

CMC_13849

AKOS015915514

CARBONEUM HYDROGENISATUM [HPUS]

MCULE-9947181734

Polyethylene, low density, 500 micron

USEPA/OPP Pesticide Code: 041901

Ethylene, Messer(R) CANGas, 99.98%

Ethylene, puriss., >=99.95% (GC)

NS00013981

NS00131932

C06547

C19503

Ethylene, refrigerated liquid (cryogenic liquid)

Ethylene, compressed [UN1962] [Flammable gas]

Q151313

Q27286698

Ethylene, refrigerated liquid (cryogenic liquid) [UN1038] [Flammable gas]

87701-65-3

The Henry's Law constant for ethylene is 0.228 atm-cu m/mole(1). This Henry's Law constant indicates that ethylene is expected to volatilize rapidly from water surfaces(2). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as 30 minutes(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 2 days(SRC). Ethylene's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Ethylene is expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 5.21X10+4 mm Hg(3).
Literature: (1) Wasik SP, Tsang W; J Phys Chem 74: 2970-6 (1970) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, DC: Taylor and Francis (1989)

The Koc of ethylene is estimated as 98(SRC), using a log Kow of 1.13(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that ethylene is expected to have high mobility in soil.
Literature: (1) Hansch C et al; Exploring QSAR. Hydrophobic, Electronic, and Steric Constants. ACS Prof Ref Book. Heller SR, consult. ed., Washington, DC: Amer Chem Soc p. 4 (1995) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 4-9 (1990) (3) Swann RL et al; Res Rev 85: 17-28 (1983)

ISOPHORONE

78-59-1

Isoacetophorone

3,5,5-Trimethylcyclohex-2-en-1-one

Isoforone

Isooctopherone

Isoforon

Izoforon

3,5,5-Trimethyl-2-cyclohexen-1-one

3,5,5-Trimethylcyclohex-2-enone

2-Cyclohexen-1-one, 3,5,5-trimethyl-

Isophoron

alpha-Isophorone

.alpha.-Isophoron

1,1,3-Trimethyl-3-cyclohexene-5-one

3,5,5-Trimethyl-2-cyclohexenone

.alpha.-Isophorone

NCI-C55618

3,5,5-Trimethyl-2-cyclohexen-1-on

FEMA No. 3553

3,5,5-Trimetil-2-cicloesen-1-one

Isophorone, 97%

NSC 403657

3,5,5-Trimethyl-2-cyclohexene-1-one

2BR99VR6WA

DTXSID8020759

CHEBI:34800

NSC4881

3,5,5-Trimethylcyclohexen-2-one-1

3,3,5-Trimethyl-2-cyclohexen-1-one

NSC-403657

Izoforon [Polish]

DTXCID40759

3,5-Trimethyl-2-cyclohexenone

Isoforone [Italian]

Caswell No. 506

3,5-Trimetil-2-cicloesen-1-one

3,5-Trimethyl-2-cyclohexen-1-one

1,3-Trimethyl-3-cyclohexene-5-one

3,5-Trimethyl-2-cyclohexene-1-one

WLN: L6V BUTJ C1 D1 D1

2-Cyclohexen-1-one,5,5-trimethyl-

CAS-78-59-1

CCRIS 1353

HSDB 619

ISOPHORONE, REAG

EINECS 201-126-0

3,5-Trimethyl-2-cyclohexen-1-on (GERMAN, DUTCH)

UNII-2BR99VR6WA

EPA Pesticide Chemical Code 047401

BRN 1280721

3,5,5-Trimethylcyclohexenone

a-Isophorone

AI3-00046

3,5,5-Trimethylcyclohexen one

alpha -isophoron

alpha -isophorone

3,5,5-Trimetil-2-cicloesen-1-one [Italian]

ISOACETOPHORON

nchem.180-comp3

3,5,5-Trimethyl-2-cyclohexen-1-on [German, Dutch]

1,5,5-Trimethyl-1-cyclohexen-3-one

ISOPHORONE [MI]

ISOPHORONE [FHFI]

ISOPHORONE [HSDB]

EC 201-126-0

SCHEMBL22522

Isophorone, >=97%, FG

4-07-00-00165 (Beilstein Handbook Reference)

BIDD:ER0627

Isophorone, analytical standard

CHEMBL1882894

FEMA 3553

3,5,5-trimethyl-cyclohex-2-enone

HY-Y0932

NSC-4881

Tox21_202312

Tox21_300050

BBL027346

MFCD00001584

NSC403657

s2998

STK801792

AKOS000120392

AKOS025243269

3,5,5-trimethylcyclohex-2-ene-1-one

3,5,5-trimethylcyclohexa-2-en-1-one

MCULE-5564101474

3,3,5-trimethyl-cyclohex-5-en-1-one

3,5,5-trimethyl-cyclohex-2-en-1-one

1,1, 3-Trimethyl-3-cyclohexene-5-one

1,3,3-TRIMETHYLCYLOHEXEN-5-ONE

3,5, 5-Trimethyl-2-cyclohexene-1-one

NCGC00164006-01

NCGC00164006-02

NCGC00164006-03

NCGC00254115-01

NCGC00259861-01

3,3,5-trimethyl-cyclohex-5 -en-1-one

AC-10580

VS-08530

1,5,5-TRIMETHYL-3-OXOCYCLOHEXENE

Isophorone, Vetec(TM) reagent grade, 97%

CS-0015924

I0151

NS00005755

EN300-20384

D72515

A839454

Q415519

W-104274

F0001-2053

Z104477948

InChI=1/C9H14O/c1-7-4-8(10)6-9(2,3)5-7/h4H,5-6H2,1-3H

The Henry's Law constant for isophorone is estimated as 6.6X10-6 atm-cu m/mole(SRC) derived from its vapor pressure, 0.438 mm Hg(1), and water solubility, 12,000 mg/l(2). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(3) is estimated as 7 days(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(3) is estimated as 52 days(SRC). Isophorone's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Isophorone is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(1).
Literature: (1) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, DC: Taylor and Francis (1989) (2) Parrish CF; Kirk-Othmer Encycl Chem Tech 3rd; NY, NY: Wiley-Intrsci 21: 377-401 (1983) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)

The Koc of isophorone is estimated as 200(SRC), using a log Kow of 1.7(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that isophorone is expected to have moderate mobility in soil.
Literature: (1) Veith GD et al; pp. 116-29 in Aquatic Toxicology. Easton JG et al, eds. Amer Soc Test Mat ASTM STP 707 (1980) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 4-9 (1990) (3) Swann RL et al; Res Rev 85: 17-28 (1983)

ISOPRENE

78-79-5

2-Methyl-1,3-butadiene

2-Methylbuta-1,3-diene

Isopentadiene

2-Methylbutadiene

2-Methyldivinyl

1,3-Butadiene, 2-methyl-

beta-Methylbivinyl

isopreno

isoterpene

Isopren

3-Methyl-1,3-butadiene

CH2=C(CH3)CH=CH2

.beta.-Methylbivinyl

NSC 9237

Naturalrubber

CCRIS 6253

HSDB 620

EINECS 201-143-3

UNII-0A62964IBU

9003-31-0

9006-04-6

DTXSID2020761

NATURAL RUBBER

CHEBI:35194

0A62964IBU

NSC-9237

DTXCID20761

NSC9237

EC 201-143-3

ISOPRENE (IARC)

ISOPRENE [IARC]

Rubber, natural

UN1218

Caoutchouc

Elastomers

Ebonite

Heveaplus

Impervia

Rubber

Latex particles

Nafka

Natural latex

India rubber

Nafka kristalgom

Dynatex LA

Dynatex GTZ

Thiokol NVT

LATZ latex

2-methyl-butadiene

Isoprene, inhibited

Harub 5LV

Heveacrumb SMR 5L

2-methyl-1

Lorival R 25

Hartex 102HR

Cartex 600

Fultite FB 010K

Fultite FB 520

Hartex 103

Fultite FB 3001

Iotex C 60

Isoprene, >=99%

Kagetex FA 2005

ISOPRENE [HSDB]

E 218 (rubber)

Mitsuwa RC paper Cement

ISOPRENE [MI]

Defo 700

Elastic materials, rubber

UNII-2LQ0UUW8IN

Lotol L 9241

2LQ0UUW8IN

Be Be Tex 1223

bmse000844

Defo 1000

ISNA 5

2-methyl-buta-1,3-diene

AMA 7

CSV 1

Isoprene, analytical standard

Mar DR 1135

68877-32-7

UN 1218 (Salt/Mix)

DRC 60

CHEMBL1566132

Isoprene (Stabilized with TBC)

WLN: 1UY1&1U1

HSDB 6772

DTXSID60185761

GLN 200

GNL 150

Isoprene (1 mg/mL in Methanol)

JLX 105

JLX 113

KDP 150

CV 50

CV 60

IR 25

IR 68

AMY37001

EINECS 232-689-0

Tox21_200067

5L-TP0203

CS 700

HC 106

MFCD00008600

AKOS000119971

CCG-266006

FB 3001

CAS-78-79-5

NCGC00091078-01

NCGC00091078-02

NCGC00257621-01

PD088096

I0160

NS00001388

EN300-19669

Q271943

Isoprene, inhibited [UN1218] [Flammable liquid]

J-509898

InChI=1/C5H8/c1-4-5(2)3/h4H,1-2H2,3H

Z104474660

Isoprene, 99%, contains <1000 ppm p-tert-butylcatechol as inhibitor

26796-44-1

9041-65-0

The Henry's Law constant for isoprene is estimated as 0.077 atm-cu m/mole(SRC) derived from its vapor pressure, 550 mm Hg(1), and water solubility, 642 mg/L(2). This Henry's Law constant indicates that isoprene is expected to volatilize rapidly from water surfaces(3). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(3) is estimated as 2.4 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(3) is estimated as 3.3 days(SRC). Isoprene's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of isoprene from dry soil surfaces may exist(SRC) based upon its vapor pressure(1).
Literature: (1) Zwolinski BJ, Wilhoit RC; Handbook of Vapor Pressures and Heats of Formation of Hydrocarbons and Related Compounds. API44-TRC101 College Station, TX: Thermodynamics Res Ctr p. 48 (1971) (2) McAuliffe C; J Phys Chem 70: 1267-75 (1966) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)

The Koc of isoprene is estimated as 61(SRC), using a log Kow of 2.42(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that isoprene is expected to have high mobility in soil.
Literature: (1) Chemicals Inspection and Testing Institute. Japan Chemical Industry Ecology - Toxicology and Information Center. ISBN 4-89074-101-1 (1992) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 4-9 (1990) (3) Swann RL et al; Res Rev 85: 17-28 (1983)

METHACROLEIN

78-85-3

Methacrylaldehyde

2-Methyl-2-propenal

2-Methylacrolein

2-Propenal, 2-methyl-

Isobutenal

2-Methylprop-2-enal

2-Methylpropenal

Acrolein, 2-methyl-

Methylacrylaldehyde

2-Methylenepropanal

Methacrylic aldehyde

Methakrylaldehyd

Methacrolein (stabilized with HQ)

.alpha.-Methacrolein

.alpha.-Methylacrolein

NSC 8260

2-methyl-propenal

9HRB24892H

NSC-8260

alpha-Methylacrolein

HSDB 182

Methakrylaldehyd [Czech]

MFCD00006974

2-Methylpropenal [Czech]

CCRIS 1153

EINECS 201-150-1

UN2396

BRN 1209258

methacroleine

Methacraldehyde

UNII-9HRB24892H

AI3-37779

2-Methylacrylaldehyde

Methacrolein, 95%

METHACRYALDEHYDE

2-Methylacrylaldehyde #

2-METHYL PROPENAL

METHACROLEIN [HSDB]

Methacrylaldehyde, inhibited

CH2=C(CH3)CHO

2-FORMYL-1-PROPENE

WLN: VHY1&U1

4-01-00-03455 (Beilstein Handbook Reference)

UN 2396 (Salt/Mix)

CHEMBL4063095

DTXSID0052540

CHEBI:88384

NSC8260

.ALPHA.-METHYLACRYLALDEHYDE

AMY28760

AKOS000119839

M0078

NS00022801

EN300-19749

H10713

Methacrolein (Stabilized with 1% Hydroquinone)

A839511

Q420234

InChI=1/C4H6O/c1-4(2)3-5/h3H,1H2,2H

Methacrolein (Stabilized with 1per cent Hydroquinone)

F2191-0163

Methacrylaldehyde, inhibited [UN2396] [Flammable liquid]

The Henry's Law constant for methacrolein is estimated as 1.9X10-4 atm-cu m/mole(SRC) from its experimental values for vapor pressure, 155 mm Hg(1), and water solubility, 50,000 mg/l(2). This value indicates that methacrolein will volatilize from water surfaces(3,SRC). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec) is estimated as approximately 5 hours(3,SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec) is estimated as approximately 4 days(3,SRC). Methacrolein's high vapor pressure(1) and Henry's Law constant(1,2,SRC) indicate that volatilization from dry and moist soil may occur(SRC).

The Koc of methacrolein is estimated as approximately 11.3(SRC), using an experimental water solubility of 50,000 mg/L(1) and a regression-derived equation(2,SRC). According to a recommended classification scheme(3), this estimated Koc value suggests that methacrolein has very high mobility in soil(SRC).

METHYL VINYL KETONE

3-Buten-2-one

78-94-4

but-3-en-2-one

Butenone

Vinyl methyl ketone

Methylene acetone

2-Butenone

Methylvinylketon

Acetyl ethylene

1-Buten-3-one

3-Butene-2-one

Methyl ethenyl ketone

Methylvinyl ketone

Methylvinylketone

3-Butenone-2

Acetone, methylene-

Ketone, methyl vinyl

gamma-Oxo-alpha-butylene

Methyl-vinyl-cetone

3-oxo-1-butene

but-1-en-3-one

methylvinylcetone

3-Oxobutene

NSC 4853

UN1251

CHEBI:48058

Delta(3)-2-butenone

CH2=CHCOCH3

25038-87-3

AR7642I1MP

CHEMBL1600824

DTXSID3025671

NSC-4853

MFCD00008777

Methgl vinyl ketone

Methylvinylketon [German]

delta(sup 3)-2-Butenone

Methyl-vinyl-cetone [French]

CCRIS 3423

HSDB 716

EINECS 201-160-6

UNII-AR7642I1MP

AI3-16048

3-butenone

methyl vinylketone

methyl-vinylketone

methylvinyl-ketone

but-3-enone

buten-2-one

g-oxo-a-Butylene

metyl vinyl ketone

3-oxo-l-butene

methly vinyl ketone

methyl-vinyl-ketone

1-butene-3-one

3-Butenen-2-one

1-Propen-3-one

3-oxo-but-1-ene

EC 201-160-6

.DELTA.3-2-BUTENONE

.gamma.-Oxo-.alpha.-butylene

DTXCID205671

Methyl vinyl ketone, stabilised

Methyl vinyl ketone, stabilized

WLN: 1V1U1

METHYL VINYL KETONE [MI]

NSC4853

BCP24759

Tox21_200363

BDBM50245462

LMFA12000018

STL299803

.DELTA.-OXO-.ALPHA.-BUTYLENE

AKOS000120352

UN 1251

UN-1251

CAS-78-94-4

NCGC00091118-01

NCGC00091118-02

NCGC00257917-01

M0460

NS00004153

3-Buten-2-one, purum, >=95.0% (GC)

EN300-19794

C20701

F71092

M-6580

Q417525

InChI=1/C4H6O/c1-3-4(2)5/h3H,1H2,2H

Methyl vinyl ketone, stabilized [UN1251] [Poison]

3-Buten-2-one (90%) (Stabilized with <1% Hydroquinone)

3-Buten-2-one, contains 0.3-1.0% hydroquinone as stabilizer, technical grade, 90%

3-Buten-2-one, contains 0.5% hydroquinone and 0.1% acetic acid as stabilizer, 99%

The Henry's Law constant for methyl vinyl ketone is 4.65X10-5 atm-cu m/mole(1). This Henry's Law constant indicates that methyl vinyl ketone is expected to volatilize from water surfaces(2). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as 18 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 8.1 days(SRC). Methyl vinyl ketone's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Methyl vinyl ketone is expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 152 mm Hg(SRC), determined from a fragment constant method(3).

Using a structure estimation method based on molecular connectivity indices(1), the Koc of methyl vinyl ketone can be estimated to be 3.8(SRC). According to a classification scheme(2), this estimated Koc value suggests that methyl vinyl ketone is expected to have very high mobility in soil.

ACRYLIC ACID

2-Propenoic acid

79-10-7

prop-2-enoic acid

Vinylformic acid

Propenoic acid

Acroleic acid

Ethylenecarboxylic acid

Propene acid

ACRYLATE

Propenoate

Glacial acrylic acid

9003-01-4

Kyselina akrylova

Acrylic acid, glacial

RCRA waste number U008

Acide acrylique

Acido acrilio

Caswell No. 009A

Carbopol 934p

Viscalex HV 30

NSC 4765

CCRIS 737

Acrylic resin

HSDB 1421

UNII-J94PBK7X8S

EINECS 201-177-9

J94PBK7X8S

Carbopol 940

BRN 0635743

ACRLYLIC ACID

DTXSID0039229

CHEBI:18308

AI3-15717

NSC-4765

DTXCID8028

Aron

Antiprex A

Versicol E9

NSC4765

EC 201-177-9

Acrylic acid resin

ACRYLIC ACID (13C3)

Acrysol ase-75

C3:1n-1

Versicol E 7

Versicol E15

4-02-00-01455 (Beilstein Handbook Reference)

Acrysol A 1

Acrysol A 3

Acrysol A 5

Acrysol A-1

Acrysol AC 5

Carbopol 960

Carboset 515

Primal Ase 60

Revacryl A191

Versicol K 11

Versicol S 25

Dispex C40

Acrysol WS-24

Cyguard 266

Joncryl 678

Jurimer AC 10H

Jurimer AC 10P

Nalfloc 636

Good-rite K 37

Revacryl A 191

Junlon 110

Viscon 103

Good-rite K 702

Good-rite K 732

Good-rite WS 801

NCGC00166246-01

Poly(acrylic acid), 25% soln in water

Synthemul 90-588

Aron A 10H

Carboset Resin No. 515

ACRYLIC ACID (IARC)

ACRYLIC ACID [IARC]

OLD 01

PA 11M

PAA-25

Carbopol

P 11H

P-11H

WS 24

Acido acrilio [Spanish]

Acide acrylique [French]

WS 801

Kyselina akrylova [Czech]

R968

UN2218

RCRA waste no. U008

allenediol

Acrysol lmw-20X

XPA

Aqueous acrylic acid

25987-55-7

Dow Latex 354

Ethene carboxylic acid

Acrylic acid, inhibited

CH2=CHCOOH

(stabilized with MEHQ)

Carbomer 934 (NF)

Carbomer 940 (NF)

Carbomer 941 (NF)

Carbopol 910 (TN)

Carbopol 934 (TN)

Carbopol 940 (TN)

Carbopol 941 (TN)

Carbomer 934P (NF)

Carbopol 934P (TN)

Carbomer 910 (USAN)

ACRYLIC ACID [MI]

Carbomer 1342 (NF)

Carbopol 1342 (TN)

ACRYLIC ACID [HSDB]

ACRYLIC ACID [INCI]

WLN: QV1U1

average Mv ~450,000

UN 2218 (Salt/Mix)

Acrylic acid, p.a., 99%

CHEMBL1213529

STR00040

Tox21_112372

LMFA01030193

MFCD00004367

NSC106034

NSC106035

NSC106036

NSC106037

NSC112122

NSC112123

NSC114472

NSC165257

NSC226569

STL281870

AKOS000118799

DB02579

MCULE-9352227082

NSC-106034

NSC-106035

NSC-106036

NSC-106037

NSC-112122

NSC-112123

NSC-114472

NSC-165257

NSC-226569

CAS-79-10-7

BP-30259

DB-220116

DB-251641

A0141

NS00001146

EN300-17959

C00511

C19501

D03392

D03393

D03394

D03395

D03396

D03397

Acrylic Acid contains 200ppm MEHQ as inhibitor

Acrylic acid, inhibited [UN2218] [Corrosive]

A830860

Q324628

Z57127944

F0001-2070

InChI=1/C3H4O2/c1-2-3(4)5/h2H,1H2,(H,4,5

Acrylic acid, anhydrous, contains 200 ppm MEHQ as inhibitor, 99%

Acrylic acid, SAJ first grade, >=97.0%, contains 190-210 ppm MEHQ as stabilizer

1204391-75-2

55927-87-2

9063-87-0

A pKa of 4.26(1) indicates acrylic acid will exist almost entirely in the anion form at pH values of 5 to 9 and therefore volatilization from water surfaces and moist soil is not expected to be an important fate process(2). The potential for volatilization of acrylic acid from dry soil surfaces may exist(SRC) based upon a vapor pressure of 3.97 mm Hg(3).
Literature: (1) Riddick JA et al; Organic Solvents: Physical Properties and Methods of Purification. Techniques of Chemistry. 4th ed. New York, NY: Wiley-Interscience (1986) (2) Doucette WJ; pp. 141-188 in Handbook of Property Estimation Methods for Chemicals. Boethling RS, Mackay D, eds, Boca Raton, FL: Lewis Publ (2000) (3) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals: Data Compilation. Design Inst Phys Prop Data, Amer Inst Chem Eng New York, NY: Hemisphere Pub Corp 5 Vol (1987)

Koc values for acrylic acid have been reported as 6 in Washington clay/loam (29% sand, 42% silt, 29% clay, 3.39% organic carbon, pH 6.0), 9 in Canfield loam (45% sand, 42% silt, 13% clay, 4.58% organic carbon, pH 6.1), 29 in Ellsworth loam (35% sand, 40% silt, 25% clay, 1.42% organic carbon, pH 7.2), 137 in Tyner loamy sand (79% sand, 14% silt, 7% clay, 0.46% organic carbon, pH 5.2), and 33 in sandy loam sediment (53% sand, 28% silt, 19% clay, 1.23% organic carbon, pH 7.5)(1) According to a classification scheme(2), these Koc values suggest that acrylic acid is expected to have very high to high mobility in soil. The pKa of acrylic acid is 4.26(3), indicating that this compound will exist almost entirely in anion form in the environment and anions generally do not adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(4).
Literature: (1) Staples CA et al; Chemosphere 40: 29-38 (2000) (2) Swann RL et al; Res Rev 85: 17-28 (1983) (3) Riddick JA et al; Organic Solvents: Physical Properties and Methods of Purification. Techniques of Chemistry. 4th ed. New York, NY: Wiley-Interscience (1986) (4) Doucette WJ; pp. 141-188 in Handbook of Property Estimation Methods for Chemicals. Boethling RS, Mackay D, eds. Boca Raton, FL: Lewis Publ (2000)

2,4,6-TRICHLOROANISOLE

87-40-1

1,3,5-Trichloro-2-methoxybenzene

Tyrene

2,4,6-Trichloro-1-methoxybenzene

TRICHLOROANISOLE

Benzene, 1,3,5-trichloro-2-methoxy-

Methyl 2,4,6-trichlorophenyl ether

Anisole, 2,4,6-trichloro-

2,4.6-Trichloroanisole

1,3,5-trichloro-2-methoxy-benzene

MFCD00000588

NSC-35142

31O3X41254

UNII-31O3X41254

EINECS 201-743-5

NSC 35142

2,6-Trichloroanisole

AI3-09173

Anisole,4,6-trichloro-

2,4,6-Trichloro-Anisole

SCHEMBL54507

1,5-Trichloro-2-methoxybenzene

DTXSID9073886

CHEBI:19333

2,4,6-Trichloroanisole, 99%

Methyl 2,6-trichlorophenyl ether

Benzene,3,5-trichloro-2-methoxy-

NSC35142

AKOS015849927

Anisole, 2,4,6-trichloro- (8CI)

2,4,6-TRICHLOROANISOLE [MI]

1,3,5-Trichloro-2-methoxybenzene, 9CI

AS-60959

SY051443

1-METHOXY-2,4,6-TRICHLOROBENZENE

DB-057000

CS-0150571

NS00008077

T0867

Benzene, 1,3,5-trichloro-2-methoxy- (9CI)

F20912

Q209191

2,4,6-Trichloroanisole 10 microg/mL in Isooctane

2,4,6-Trichloroanisole 100 microg/mL in Methanol

2,4,6-Trichloroanisole 1000 microg/mL in Methanol

2,4,6-Trichloroanisole, PESTANAL(R), analytical standard

InChI=1/C7H5Cl3O/c1-11-7-5(9)2-4(8)3-6(7)10/h2-3H,1H

CARVEOL

99-48-9

p-Mentha-6,8-dien-2-ol

p-Mentha-1,8-dien-6-ol

2-Methyl-5-(1-methylethenyl)-2-cyclohexen-1-ol

L-Carveol

(-)-Carveol

1-Methyl-4-isopropenyl-6-cyclohexen-2-ol

2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-ol

p-Mentha-1(6),8-dien-2-ol

2-methyl-5-prop-1-en-2-ylcyclohex-2-en-1-ol

5-Isopropenyl-2-methyl-2-cyclohexen-1-ol

2-Cyclohexen-1-ol, 2-methyl-5-(1-methylethenyl)-

5-isopropenyl-2-methylcyclohex-2-en-1-ol

2-Methyl-5-isopropenyl-2-cyclohexen-1-ol

NSC 68313

2-Methyl-5-(prop-1-en-2-yl)cyclohex-2-enol

6,8-p-Menthadien-2-ol

DTXSID3024736

CHEBI:23046

(Z)-Carveol

FEMA No. 2247

MFCD00062993

EINECS 202-757-4

2-Methyl-5(1-methylethenyl)cyclohex-2-ene-1-ol

2-Methyl-5-[1-methylethenyl]-2-cyclohexen-1-ol

(1S-trans)-2-Methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol

laevo-carveol

CCRIS 6219

p-Mentha-6,8-dien-2-ol (VAN)

BRN 1861032

a carveol

AI3-27596

MFCD00869995

laevo-(Z)-carveol

p-Mentha-6, l-

UPCMLD-DP073

Allyl 4-aminobutylcarbamate

SCHEMBL56868

2-06-00-00102 (Beilstein Handbook Reference)

L-p-mentha-6-8-dien-2-ol

DTXCID104736

GTPL6417

CHEMBL1385229

UPCMLD-DP073:001

FEMA 2247

NSC68313

Tox21_200175

NSC-68313

AKOS015915605

CS-W018086

HY-W017370

CAS-99-48-9

NCGC00091404-01

NCGC00091404-03

NCGC00091404-04

NCGC00257729-01

WLN: L6UTJ AQ B1 EY1 & U1

AS-66951

SY319013

1H-Imidazol-1-amine, 2-methyl-4-nitro-

DB-045454

DB-080605

NS00012077

2-Methyl-5-(1-propen-2-yl)-2-cyclohexenol

D77822

2-Cyclohexen-1-ol,2-methyl-5-(1-methylethenyl)-

Q2920205

20307-86-2

4-Vinylcyclohexene

100-40-3

4-VINYL-1-CYCLOHEXENE

Cyclohexene, 4-ethenyl-

4-Ethenylcyclohexene

4-vinylcyclohex-1-ene

Butadiene dimer

Cyclohexenylethylene

Cyclohexene, 4-vinyl-

4-Ethenyl-1-cyclohexene

4-Vinylcyclohexene-1

1-Vinylcyclohexene-3

4-Vinyl cyclohexene

1-Cyclohexene, 4-vinyl-

Ethenyl-1-cyclohexene

NCI-C54999

1,2,3,4-Tetrahydrostyrene

Vinylcyclohexene, 4-

NSC 15760

1-Vinyl-3-cyclohexene

1-Vinylcyclohex-3-ene

212JQJ15PS

DTXSID3021437

CHEBI:82377

NSC-15760

CCRIS 1422

HSDB 2872

4-ethenylcyclohex-1-ene

EINECS 202-848-9

BRN 1901553

UNII-212JQJ15PS

AI3-08499

4-vinylcylohexene

4 vinyl cyclohexene

4-vinyl-cyclohexene

5-Ethenylcyclohexene

4-VINYLCYCLOHENE

1,3,4-Tetrahydrostyrene

EC 202-848-9

4-VCH

WLN: L6UTJ D1U1

4-05-00-00406 (Beilstein Handbook Reference)

DTXCID601437

4-Vinyl-1-cyclohexene, 99%

CHEMBL1330194

4-VINYLCYCLOHEXENE [IARC]

NSC15760

Tox21_200388

MFCD00001576

AKOS015903842

MCULE-1027409234

NCGC00091539-01

NCGC00091539-02

NCGC00091539-03

NCGC00257942-01

CAS-100-40-3

LS-13442

4-Vinyl-1-cyclohexene, analytical standard

DS-015484

NS00008744

V0023

4-Vinyl-1-cyclohexene (stabilized with BHT)

C19310

D92779

EN300-123688

4-Vinyl-1-cyclohexene 2000 microg/mL in Methanol

J-000127

Q4637205

The Henry's Law constant for 4-vinylcyclohexene is estimated as 4.5X10-2 atm-cu m/mole(SRC), derived from its vapor pressure, 15.7 mm Hg(1), and water solubility, 50 mg/l(2). This Henry's Law constant indicates that 4-vinylcyclohexene is expected to volatilize rapidly from water surfaces(3). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(3) is estimated as 1.1 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(3) is estimated as 4.1 days(SRC). However, volatilization from water surfaces is expected to be attenuated by adsorption to suspended solids and sediment in the water column. The estimated volatilization half-life from a model pond is 19 days if adsorption is considered(4). 4-Vinylcyclohexene's estimated Henry's Law constant(1,2) indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of 4- vinylcyclohexene from dry soil surfaces may exist(SRC) based upon a vapor pressure of 15.7 mm Hg(1).

The Koc of 4-vinylcyclohexene is estimated as 3300(SRC), using a measured log Kow of 3.93(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that 4-vinylcyclohexene is expected to have slight mobility in soil(SRC).

1-BUTENE

But-1-ene

Ethylethylene

106-98-9

BUTENE

1-Butylene

Butene-1

alpha-Butylene

alpha-Butene

9003-28-5

1-C4H8

CCRIS 8970

HSDB 179

.alpha.-Butene

.alpha.-Butylene

25167-67-3

EINECS 203-449-2

UNII-LY001N554L

CHEBI:48362

LY001N554L

DTXSID1026746

EC 203-449-2

1-Butene (ca. 10% in Hexane)

Butene, 1-

MFCD00009383

1-n-Butene

Actipol E6

61788-35-0

but-1-en-3-yl

BUTENE [INCI]

1-BUTENE [HSDB]

1-BUTENE [MI]

1-Butene, >=99%

CHEMBL117210

DTXCID606746

1-Butene, >=99.6%

But-1-ene (10% in Hexanes)

DTXSID10175879

DTXSID80983963

1-Butene (ca. 10% in Toluene)

1-Butene, >=99.0% (GC)

AKOS009156841

MCULE-8167907130

DB-040719

B0689

B4410

B4411

NS00009034

InChI=1/C4H8/c1-3-4-2/h3H,1,4H2,2H

Q2468763

6993-22-2

The Henry's Law constant for 1- butene is 0.245 atm-cu m/mole(1). This Henry's Law constant indicates that 1- butene is expected to volatilize rapidly from water surfaces(2). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as 45 minutes (SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 3 days(SRC). 1-Butene's Henry's Law constant(1) indicates that volatilization from moist soil surfaces may occur(SRC). 1-Butene is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 2250 mm Hg(3).
Literature: (1) Yaws CL; Thermodynamics and Physical Property Data, Houston, TX: Gulf Publ Co pp. 217 (1992) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals: Data Compilation. Design Inst Phys Prop Data, Amer Inst Chem Eng NY, NY: Hemisphere Pub Corp 5 Vol (1989)

Using a structure estimation method based on molecular connectivity indices(1), the Koc for 1-butene can be estimated to be 44(SRC). According to a classification scheme(2), this estimated Koc value suggests that 1-butene is expected to have very high mobility in soil.
Literature: (1) Meylan WM et al; Environ Sci Technol 26: 1560-67 (1992) (2) Swann RL et al; Res Rev 85: 17-28 (1983)

1,3-BUTADIENE

Buta-1,3-diene

106-99-0

Divinyl

BUTADIENE

Biethylene

Vinylethylene

Erythrene

Bivinyl

Pyrrolylene

Butadieen

Butadien

Buta-1,3-dien

Buta-1,3-dieen

alpha,gamma-Butadiene

Butadiene monomer

9003-17-2

NCI-C50602

1,3-butadien

Butadiene-1,3-uninhibited

Buta-1,3-dien [German]

CCRIS 99

Butadiene, 1,3-

HSDB 181

JSD5FGP5VD

.alpha.,.gamma.-Butadiene

EINECS 203-450-8

CHEBI:39478

UNII-JSD5FGP5VD

1,3-BUTADIENE-2,3-D2

CH2=CHCH=CH2

CH2=CH-CH=CH2

UN 1010

1,3-Butadiene, homopolymer

1,3-Butadiene (ca. 15% in Toluene)

DTXSID3020203

130983-70-9

1983-06-8

25339-57-5

1,3-Butadiene (ca. 15% in Hexane)

EC 203-450-8

1,3-BUTADIENE (IARC)

1,3-BUTADIENE [IARC]

vinyl ethylene

MFCD00008659

1,3 butadiene

Butadieen [Dutch]

Butadien [Polish]

26952-74-9

alpha-gamma-butadiene

1,3-Butadiene, puriss., >=99.5% (GC)

Buta-1,3-dieen [Dutch]

butadiene-1,3

alpha, gamma-butadiene

BUTADIENE [INCI]

1,3-Butadiene 95%

alpha,<>-Butadiene

CH22CH1CH2CH2

BUTADIENES, STABILIZED

DTXCID10203

1,3-Butadiene, >=99%

1,3-BUTADIENE [MI]

CHEMBL537970

1,3-BUTADIENE [HSDB]

CHEBI:39479

1,3-Butadiene, >=99.6%

BUTADIENE-1, 3, STABILIZED

1,3-BUTADIENE, (STABILIZED)

1,3-Butadiene, purum, >=98.0%

AKOS007930655

68514-37-4

1,3-Butadiene 100 microg/mL in Methanol

1,3-Butadiene 200 microg/mL in Methanol

1,3-Butadiene 1000 microg/mL in Methanol

B0675

B4358

B4359

B4835

NS00007558

1,3-Butadiene 10000 microg/mL in Methanol

InChI=1/C4H6/c1-3-4-2/h3-4H,1-2H

Q161503

1,3-Butadiene (~15per cent by weight in Toluene)

1,3-Butadiene 10 microg/mL in N,N-Dimethylacetamide

1,3-Butadiene 50 microg/mL in N,N-Dimethylacetamide

1,3-Butadiene 150 microg/mL in N,N-Dimethylacetamide

1,3-Butadiene 250 microg/mL in N,N-Dimethylacetamide

1,3-Butadiene 400 microg/mL in N,N-Dimethylacetamide

1,3-Butadiene (ca. 13% in Tetrahydrofuran, ca. 2mol/L)

The Henry's Law constant for 1,3-butadiene is estimated as 0.0736 atm-cu m/mole(SRC) derived from its vapor pressure, 2052 mm Hg(1), and water solubility, 735 mg/L(2). This Henry's Law constant indicates that 1,3-butadiene is expected to volatilize rapidly from water surfaces(3). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(3) is estimated as 2.2 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(3) is estimated as 2.9 days(SRC). 1,3-Butadiene's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). 1,3-Butadiene is expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(1).

Using a structure estimation method based on molecular connectivity indices(1), the Koc of 1,3-butadiene can be estimated to be 40(SRC). According to a classification scheme(2), this estimated Koc value suggests that 1,3-butadiene is expected to have very high mobility in soil.

ACROLEIN

Acrylaldehyde

2-Propenal

107-02-8

Propenal

Acrylic aldehyde

prop-2-enal

Allyl aldehyde

Ethylene aldehyde

Aqualin

Magnacide H

Acraldehyde

Slimicide

2-Propen-1-one

Aqualine

Crolean

Prop-2-en-1-al

Magnacide

Acquinite

Biocide

Acrylaldehyd

Acroleina

Acroleine

Akrolein

Akroleina

Papite

Aldeide acrilica

Aldehyde acrylique

Acraldehydeacroleina

NSC 8819

Rcra waste number P003

Propenaldehyde

trans-Acrolein

Caswell No. 009

Magnacide B

Aldehyde, Allyl

Aldehyde, Acrylic

Aldehyde, Ethylene

Magnacide H and B

CCRIS 3278

HSDB 177

Acrolein (stabilized with hydroquinone)

UN 1092

CHEBI:15368

2-Propenaldehyde

EINECS 203-453-4

UNII-7864XYD3JJ

EPA Pesticide Chemical Code 000701

7864XYD3JJ

25068-14-8

DTXSID5020023

AI3-24160

CH2=CHCHO

NSC-8819

CHEMBL721

DTXCID8023

EC 203-453-4

ACROLEIN (IARC)

ACROLEIN [IARC]

ACROLEIN (MART.)

ACROLEIN [MART.]

Akrolein [Czech]

Propenal [Czech]

Acrolein, analytical standard

Akroleina [Polish]

Acroleina [Italian]

Acrylaldehyd [German]

2 Propenal

Acroleine [Dutch, French]

Aldeide acrilica [Italian]

Propadien-1-ol

Aldehyde acrylique [French]

Acrolein, inhibited

Propenal, inhibited

Acraldehydeacroleina [Italian]

UN1092

RCRA waste no. P003

Acrylic aldehyde, inhibited

allol

Acrylehyde

Allylaldehyde

Acrehyde

Acrylehyd

Aerolein

Acrolein Monomer

2-propen-1-al

prop-2-en-1-one

81788-96-7

ACROLEIN [HSDB]

ACROLEIN [INCI]

ACROLEIN [MI]

Epitope ID:143621

WLN: VH1U1

Acroleine(DUTCH, FRENCH)

trans-Acrolein Formylethylene

GTPL2418

DTXSID50526220

NSC8819

Acrolein 5000 microg/mL in Water

BCP07056

STR00291

Acrolein 100 microg/mL in Acetone

Tox21_200984

BDBM50010912

Acrolein 1000 microg/mL in Methanol

Acrolein 5000 microg/mL in Methanol

AKOS000120766

Acrolein, 96%, stab with hydroquinone

NCGC00091484-01

NCGC00091484-02

NCGC00258537-01

BP-14004

CAS-107-02-8

Acrolein, inhibited [UN1092] [Poison]

DB-026460

A0137

NS00009782

C01471

InChI=1/C3H4O/c1-2-3-4/h2-3H,1H

A801558

Q342790

Acrolein, contains hydroquinone as stabilizer, 90%

Acrolein Solution, 5000 microg/mL in Methanol, Second Source

Acrolein, stabilized with 3 wt% water, 1000ppm hydroquinone, stored over Copper

The Henry's Law constant for acrolein is 1.22X10-4 atm-cu m/mole(1). This Henry's Law constant indicates that acrolein is expected to volatilize from water surfaces(2). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as 7.6 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 4.6 days(SRC). Volatilization is likely to be the major route of acrolein's dissipation from water(3). Acrolein's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Acrolein is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 274 mm Hg(4).

Using a structure estimation method based on molecular connectivity indices(1), the Koc of acrolein can be estimated to be 1.0(SRC). According to a classification scheme(2), this estimated Koc value suggests that acrolein is expected to have very high mobility in soil.

2,4,4-TRIMETHYL-1-PENTENE

Diisobutylene

107-39-1

2,4,4-Trimethylpent-1-ene

25167-70-8

Pentene, 2,4,4-trimethyl-

1-Pentene, 2,4,4-trimethyl-

2,4,4-TRIMETHYLPENTENE

Diisobutene

2,2,4-Trimethyl-4-pentene

1-Methyl-1-neopentylethylene

NSC-8701

2,4,4-trimethylpentene-1

N69L73ADVF

DTXSID4026765

NSC-73942

2,4-Trimethyl-1-pentene

2,4-Trimethyl-4-pentene

1-Pentene,4,4-trimethyl-

MFCD00008855

HSDB 1442

EINECS 203-486-4

NSC 73942

UNII-N69L73ADVF

BRN 1098309

a-Diisobutylene

AI3-30049

Diisobutylene (DIB)

DSSTox_CID_6765

Isooctene(7ci,8ci,9ci)

DSSTox_RID_78589

TMP-1

DSSTox_GSID_27851

4-01-00-00892 (Beilstein Handbook Reference)

2,4,4 trimethyl-1-pentene

2,4,4-trimethyl-pentene-1

DTXCID806765

CHEMBL3186786

NSC8701

NSC73942

(tert-C4H9)CH2C(CH3)=CH2

Tox21_200435

Tox21_202554

2,4,4-Trimethyl-1-pentene, 96%

2,4,4-Trimethyl-1-pentene, 99%

AKOS015903731

NCGC00166004-01

NCGC00166004-02

NCGC00257989-01

NCGC00260103-01

CAS-107-39-1

LS-13500

CAS-25167-70-8

2,4,4-TRIMETHYL-1-PENTENE [HSDB]

NS00005687

T0665

D92377

J-001894

Q3030100

W-109188

InChI=1/C8H16/c1-7(2)6-8(3,4)5/h1,6H2,2-5H

1-Pentene, 2,4,4-trimethyl-; 2,4,4-Trimethyl-1-pentene; 1-Methyl-1-neopentylethylene; 2,2,4-Trimethyl-4-pentene; NSC 73942; NSC 8701

Diisobutylene, technical, >=90% (3 parts 2,4,4-trimethyl-1-pentene + 1 part 2,4,4-trimethyl-2-pentene, GC)

The Henry's Law constant for 2,4,4-trimethyl-1-pentene is estimated as 0.746 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that 2,4,4-trimethyl-1-pentene is expected to volatilize rapidly from water surfaces(2). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as 1.082 hr hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 4.2 days(SRC). 2,4,4-Trimethyl-1-pentene's Henry's Law constant(1) indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of 2,4,4-trimethyl-1-pentene from dry soil surfaces may exist(SRC) based upon a vapor pressure of 44.7 mm Hg(3).
Literature: (1) Meylan WM, Howard PH; Environ Toxicol Chem 10: 1283-93 (1991) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, DC: Taylor and Francis (1989)

Using a structure estimation method based on molecular connectivity indices(1), the Koc for 2,4,4-trimethyl-1-pentene can be estimated to be about 275(SRC). According to a classification scheme(2), this estimated Koc value suggests that 2,4,4-trimethyl-1-pentene is expected to have moderate mobility in soil.
Literature: (1) Meylan WM et al; Environ Sci Technol 26: 1560-67 (1992) (2) Swann RL et al; Res Rev 85: 23 (1983)

VINYL ACETATE

Ethenyl acetate

108-05-4

Acetic acid ethenyl ester

Acetic acid vinyl ester

Ethenyl ethanoate

Acetoxyethene

Acetoxyethylene

1-Acetoxyethylene

Vinyl acetate monomer

Vinyl ethanoate

Vinyl A monomer

Vinylacetat

Vinylacetate

9003-20-7

Zeset T

Vinylacetaat

Acetic acid, ethenyl ester

Octan winylu

Acetate de vinyle

Vinyl acetate H.Q.

Ethanoic acid, ethenyl ester

Vinile (acetato di)

Vinyle (acetate de)

VyAc

Acetic acid, vinyl ester

Vinylester kyseliny octove

Acetic acid, ethylene ether

NSC 8404

Vinylazetat

CCRIS 1306

HSDB 190

EINECS 203-545-4

Everflex 81L

Essigsaeurevinylester

UNII-L9MK238N77

Vinnapas A 50

DTXSID3021431

CHEBI:46916

AI3-18437

L9MK238N77

NSC-8404

CH3CO2CH=CH2

Unocal 76 Res S-55

Vinyl ester of acetic acid

Unocal 76 Res 6206

DTXCID201431

VAC

EC 203-545-4

VINYL ACETATE (IARC)

VINYL ACETATE [IARC]

Vinylacetaat [Dutch]

Vinylacetat [German]

Octan winylu [Polish]

Vinyl acetate, analytical standard

VyAr

Acetate de vinyle [French]

Vinyle (acetate de) [French]

Vinile (acetato di) [Italian]

Acetic Acid Vinyl Ester Monomer

Vinylester kyseliny octove [Czech]

UN1301

Vinile

Vinyle

Vinile(acetato di)

Vinylacetat(german)

Vinyle(acetate de)

Vinyl acetate, CP

PONAL

Ethenyl acetate, 9CI

VINYL ACETATE HQ

Vinyl acetate, inhibited

Plyamul 40305-00

VINYL ACETATE [MI]

VINYL ACETATE [HSDB]

VINYL ACETATE [INCI]

UN 1301 (Salt/Mix)

WLN: 1VO1U1

RP 251 (ESTER)

CHEMBL1470323

VINYL ACETATE, STABILIZED

NSC8404

Tox21_200817

BBL036266

MFCD00008713

RP 251

STL264216

AKOS009120081

MCULE-7626795765

NCGC00091098-01

NCGC00091098-02

NCGC00258371-01

CAS-108-05-4

COPOVIDONE IMPURITY C [EP IMPURITY]

Vinyl Acetate 2000 microg/mL in Methanol

Vinyl Acetate Monomer (stabilized with HQ)

A0045

NS00008176

EN300-27348

C19309

A801803

Q377339

J-002050

Vinyl Acetate(Stabilized with 8-12 ppm Hydroquinone)

F8880-1173

InChI=1/C4H6O2/c1-3-6-4(2)5/h3H,1H2,2H

Vinyl acetate, inhibited [UN1301] [Flammable liquid]

Vinyl Acetate contains 3-20 ppm hydroquinone as inhibitor

Vinyl acetate, European Pharmacopoeia (EP) Reference Standard

Vinyl acetate, contains 3-20 ppm hydroquinone as inhibitor, >=99%

93196-02-2

VAM

The Henry's Law constant for vinyl acetate is estimated as 5.1X10-4 atm-cu m/mole(SRC) derived from its vapor pressure, 90.2 mm Hg at 20 deg C(1), and water solubility, 20,000 mg/L(2). This Henry's Law constant indicates that vinyl acetate is expected to volatilize rapidly from water surfaces(3). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(3) is estimated as 4 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(3) is estimated as 4.2 days(SRC). The Henry's Law constant of vinyl acetate indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of vinyl acetate from dry soil surfaces may exist based upon its vapor pressure(1).
Literature: (1) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals: Data Compilation. Design Institute Phys Prop Data, Amer Inst Chem Eng. New York, NY: Hemisphere Pub Corp (1989) (2) Riddick JA et al; Techniques of Chemistry: Organic Solvents, Physical Properties and Methods of Purification. 4th edition. New York, NY: John Wiley & Sons (1986) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)

The Koc of vinyl acetate is estimated as approximately 60(SRC), using a log Kow of 0.73(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that vinyl acetate is expected to have high mobility in soil(SRC).
Literature: (1) Hansch C et al; Exploring QSAR, Hydrophobic, Electronic, and Steric Constants. ACS Prof Ref Book. Washington,DC: Amer Chem Soc (1995) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington DC: Amer Chem Soc pp. 4-9 (1990) (3) Swann RL et al; Res Rev 85: 23 (1983)

1-PENTENE

Pent-1-ene

109-67-1

PENTENE

Propylethylene

1-n-Pentene

.alpha.-n-Amylene

Pentene-1

ALP8M0LU81

DTXSID7025849

MFCD00003567

alpha-Amylene

alpha-n-Amylene

1-Pentylene

1-Amylene

68814-91-5

HSDB 1086

Alkenes, C5-9 alpha-

EINECS 203-694-5

UNII-ALP8M0LU81

pentaene

Alkenes, C5-9 .alpha.-

?1-Pentene

EINECS 272-344-1

pent-4-ene-1

1-Pentene 95

1-Pentene, 98%

1-PENTENE [HSDB]

1-PENTENE [MI]

EC 203-694-5

PENTENE, 1-N-

1-Pentene, analytical standard

CHEMBL295337

DTXCID905849

DTXSID60170455

EINECS 271-255-5

Tox21_200280

1-Pentene, >=98.5% (GC)

AKOS009157547

1-C5H10

FD10489

NCGC00090824-01

NCGC00090824-02

NCGC00257834-01

CAS-109-67-1

NS00006222

P0316

EN300-119395

J-002314

Q6018906

InChI=1/C5H10/c1-3-5-4-2/h3H,1,4-5H2,2H

25587-78-4

The Henry's Law constant for 1-pentene calculated from its vapor pressure, 635 mm Hg(1), and water solubility, 148 mg/l(2), is 0.40 atm-cu m/mole (SRC). This Henry's Law constant indicates that 1-pentene should volatilize rapidly from water surfaces(3). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(3) is estimated as 2.4 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(3) is estimated as 3.3 days(SRC). 1-Pentene's Henry's Law constant(1,2) indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of 1-pentene from dry soil surfaces exists based upon its vapor pressure of 635 mm Hg(1).
Literature: (1) Perry RH et al; Perry's Chemical Engineers' Handbook NY, NY: McGraw Hill (1984) (2) Yalkowsky SH, Dannenfelser RM; Aquasol Data Base of Water Solubility Ver 5, Tuscon,. AZ: Univ Arizona, College of Pharmacy (1992) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)

Sol in all proportions in alcohol, ether, and benzene
Literature: Budavari, S. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Whitehouse Station, NJ: Merck and Co., Inc., 1996., p. 1225
Literature: #Miscible in ethanol and ethyl ether, soluble in benzene.
Literature: Lide, D.R. (ed.). CRC Handbook of Chemistry and Physics. 79th ed. Boca Raton, FL: CRC Press Inc., 1998-1999., p. 3-247
Literature: #In water, 148 mg/l @ 25 deg C
Literature: Yalkowsky SH, Dannenfelser RM; The AQUASOL dATAbASE of Aqueous Solubility. Fifth ed, Tucson, AZ: Univ AZ, College of Pharmacy (1992)

Using a structure estimation method based on molecular connectivity indices(1), the Koc for 1-pentene can be estimated to be 81(SRC). According to a classification scheme(2), this estimated Koc value suggests that 1-pentene is expected to have high mobility in soil.
Literature: (1) Meylan WM et al; Environ Sci Technol 26: 1560-67 (1992) (2) Swann RL et al; Res Rev 85: 17-28 (1983)

CYCLOHEXENE

110-83-8

Tetrahydrobenzene

Cyclohex-1-ene

Benzene tetrahydride

1,2,3,4-Tetrahydrobenzene

Benzenetetrahydride

Hexanaphthylene

Cykloheksen

Benzene, tetrahydro-

1-Cyclohexene

3,4,5,6-Tetrahydrobenzene

Zyklohexen

NSC 24835

12L0P8F7GN

CHEBI:36404

NSC-24835

Cykloheksen [Polish]

25012-94-6

HSDB 1624

EINECS 203-807-8

UN2256

BRN 0906737

cylcohexene

UNII-12L0P8F7GN

cyclo hexene

cyclo-hexene

cyclohexane N

AI3-03146

CCRIS 8739

2-cyclohexen

MFCD00001539

UN 2256

CYCLOHEXENE [MI]

1,3,4-Tetrahydrobenzene

WLN: L6UTJ

CYCLOHEXENE [HSDB]

EC 203-807-8

4-05-00-00218 (Beilstein Handbook Reference)

CHEMBL16396

Cyclohexene, analytical standard

DTXSID9038717

AMY17792

NSC24835

STL445673

AKOS000119959

AKOS025243963

MCULE-3564016252

BP-31020

Cyclohexene [UN2256] [Flammable liquid]

NS00008978

EN300-19682

A802251

Cyclohexene, inhibitor-free, ReagentPlus(R), 99%

Q413328

J-002481

F0001-0225

Z104474726

Cyclohexene, contains 100 ppm BHT as inhibitor, >=99.0%

InChI=1/C6H10/c1-2-4-6-5-3-1/h1-2H,3-6H