Phenylmethanal benzenecarboxaldehyde

Benzenecarboxaldehyde

Phenylformaldehyde

PENTADEOTERO BENZALDEHYDE

benzanoaldehyde

Benzenecarbonal

Benzenemethylal

Benzylaldehyde

Phenylmethanal

Phenylmethanone

benzaidehyde

benzaldehvde

benzaldehyde

Benzene carboxaldehyde

Benzyaldehyde

Benzadehyde

benzaldehyd

Benzaldehyde Natural

Benzene carbaldehyde

Natural Benzaldehyde

Aromatic aldehyde

HUMNYLRZRPPJDN-UHFFFAOYSA-N

Benzaldehyde FFC

Benzaldehyde, analytical standard

Benzene methylal

Benzoic aldehyde

Benzoyl hydride

Almond artificial essential oil

Bitter almond

Artificial almond oil

Benzoic acid aldehyde

HBX

Artificial bitter almond oil

bitter almond oil synthetic

(phenyl)methanone

Artificial essential oil of almond

Ben zoyl hydride

Artifical essential oil of almond

2vj1

Benzaldehyde (natural)

Ethereal oil of bitter almonds

SCHEMBL573

Synthetic oil of bitter almond

AC1L18SM

AC1Q6PV7

Benzaldehyde [USAN]

Benzaldehyde, pharmaceutical secondary standard; traceable to USP

Bitter almond oil, synthetic

Oil Of bitter almond

Benzaldehyde (NF)

NATURAL RSTD CASSIA OIL DIST FLAVOR

WLN: VHR

Benzaldehyde, European Pharmacopoeia (EP) Reference Standard

KSC176K2J

ACMC-1C91Y

CHEMBL15972

LS-27

NSC7917

UN1990

B2379

BDBM60953

Benzaldehyde, United States Pharmacopeia (USP) Reference Standard

CTK0H6524

HMDB06115

HSDB 388

nchembio814-comp15

TA269SD04T

BIDD:ER0249

LS41490

RP18863

C00193

C00261

CCRIS 2376

D02314

DSSTox_CID_134

UNII-TA269SD04T

ZINC895145

AK109012

BENZALDEHYDE REACTION PRODUCTS WITH HEPTANAL DISTN. LIGHTS

DTXSID8039241

NA 1989

NSC 7917

NSC-7917

OR035988

OR192667

PL039416

A800226

Benzaldehyde, AR, >=99%

Benzaldehyde, LR, >=99%

CHEBI:17169

NCI-C56133

AJ-24149

ANW-14310

DSSTox_GSID_39241

SC-19173

BDBM50139371

Caswell No. 076

DSSTox_RID_79432

MFCD00003299

MFCD00801585

ZINC00895145

AI3-09931

Benzaldehyde, purified by redistillation, >=99.5%

Benzaldehyde, ReagentPlus(R), >=99%

DB-023673

KB-250682

LT00939687

ST24030100

TC-103055

AKOS000119172

EPA Pesticide Chemical Code 008601

ghl.PD_Mitscher_leg0.170

I01-1667

I14-7330

FEMA No. 2127

FT-0622622

Benzaldehyde, >=98%, FG, FCC

Benzaldehyde, for synthesis, 95.0%

I14-90980

Benzaldehyde, 98% 250g

Benzaldehyde, SAJ special grade, >=98.0%

Tox21_113069

Tox21_113244

Tox21_200634

100-52-7

Ald3-H_000012

Benzaldehyde, Vetec(TM) reagent grade, 98%

F1294-0144

MCULE-7744113682

NCGC00091819-01

NCGC00091819-02

NCGC00091819-03

NCGC00258188-01

Benzaldehyde, natural, >=98%, FCC, FG

CAS-100-52-7

EINECS 202-860-4

55279-75-9

SR-01000944375

Ald3.1-H_000160

Ald3.1-H_000479

Ald3.1-H_000798

5044-EP2269979A1

5044-EP2269990A1

5044-EP2272491A1

5044-EP2272827A1

5044-EP2275404A1

5044-EP2275411A2

5044-EP2275412A1

5044-EP2277858A1

5044-EP2277865A1

5044-EP2277878A1

5044-EP2281818A1

5044-EP2284157A1

5044-EP2286915A2

5044-EP2287152A2

5044-EP2287159A1

5044-EP2289868A1

5044-EP2292593A2

5044-EP2295402A2

5044-EP2295410A1

5044-EP2295441A2

5044-EP2298767A1

5044-EP2298776A1

5044-EP2301534A1

5044-EP2301536A1

5044-EP2301538A1

5044-EP2305625A1

5044-EP2305629A1

5044-EP2305662A1

5044-EP2305679A1

5044-EP2305687A1

5044-EP2305769A2

5044-EP2305808A1

5044-EP2308562A2

5044-EP2311451A1

5044-EP2311455A1

5044-EP2311806A2

5044-EP2311840A1

5044-EP2314295A1

5044-EP2314586A1

5044-EP2314587A1

5044-EP2314593A1

5044-EP2316450A1

5044-EP2316832A1

5044-EP2316833A1

5044-EP2371831A1

5044-EP2374454A1

5044-EP2374783A1

5044-EP2377841A1

5044-EP2380871A1

Benzaldehyde, purum, >=98.0% (GC)

53585-EP2305651A1

53585-EP2308854A1

Benzaldehyde [UN1990] [Class 9]

Benzaldehyde on polystyrene, 0.8-1.5 mmol/g

125826-EP2287158A1

125826-EP2295422A2

SR-01000944375-1

Benzaldehyde [UN1990] [Class 9]

Benzaldehyde, puriss. p.a., >=99.0% (GC)

InChI=1/C7H6O/c8-6-7-4-2-1-3-5-7/h1-6

The Henry's Law constant for benzaldehyde is 2.67X10-5 atm-cu m/mole(1). This Henry's Law constant indicates that benzaldehyde 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 1.5 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)(2) is estimated as 14 days(SRC). Benzaldehyde's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Benzaldehyde is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 1.27 mm Hg at 25 deg C(3).
Literature: (1) Betterton EA, Hoffmann MR; Environ Sci Technol 22: 1415-8 (1988) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Ambrose D et al; J Chem Therm 7: 1143-57 (1975)

Using a structure estimation method based on molecular connectivity indices(1), the Koc of benzaldehyde can be estimated to be 11(SRC). According to a classification scheme(2), this estimated Koc value suggests that benzaldehyde is expected to have very high mobility in soil.
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Nov, 2012. Available from, as of May 30, 2016: http://www2.epa.gov/tsca-screening-tools/ (2) Swann RL et al; Res Rev 85: 17-28 (1983)

Methylmercaptaan

Mercaptomethane

Metilmercaptano

methylsulfanium

Methylmercaptan

Methaanthiol

Thiomethanol

methanethiol

Methanethiole

Thiomethane

Mercaptan methylique

Methanthiol

Methvtiolo

(Mercaptomethyl)polystyrene

LSDPWZHWYPCBBB-UHFFFAOYSA-N

Methyl sulfhydrate

Thiomethyl alcohol

Methyl thioalcohol

METHYL MERCAPTAN

methyl-mercaptan

methane thiol

methyl thiol

methyl-thiol

Methanethiol, purum

CH3SH

Methanethiol-S-d

Mercaptan C1

Metilmercaptano [Italian]

Metilmercaptano [Spanish]

Methylmercaptaan [Dutch]

Methanthiol [German]

Methvtiolo [Italian]

Z22

Mercaptan methylique [French]

AC1L1A8B

Methaanthiol [Dutch]

Methyl mercaptan (natural)

UN1064

CTK2H7493

HSDB 813

HMDB03227

C00409

2X8406WW9I

RCRA waste number U153

OR332408

NSC229573

OR000105

OR164971

OR230018

OR230158

UN 1064

DTXSID5026382

Methanethiol, >=98.0%

LS-2938

CHEBI:16007

UNII-2X8406WW9I

Methanethiol, 98.0%

AN-23827

SC-46829

NSC-229573

AKOS009157032

RCRA waste no. U153

BRN 1696840

FEMA No. 2716

FT-0696326

74-93-1

EINECS 200-822-1

63933-47-1

17719-48-1

InChI=1/CH4S/c1-2/h2H,1H

Methyl mercaptan [UN1064] [Poison gas]

(Mercaptomethyl)polystyrene, extent of labeling: ~2.0 mmol/g S loading

5188-07-8 (hydrochloride salt)

Methyl mercaptan [UN1064] [Poison gas]

4-01-00-01273 (Beilstein Handbook Reference)

21094-80-4 (mercury(2+) salt)

35029-96-0 (lead(2+) salt)

The Henry's Law constant for methyl mercaptan is estimated as 0.0031 atm-cu m/mole(SRC) derived from its vapor pressure, 1,510 mm Hg(1), and water solubility, 15,400 mg/L(2). This Henry's Law constant indicates that methyl mercaptan 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 0.8 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 2.8 days(SRC). Methyl mercaptan's Henry's Law constant indicates that volatilization from moist soil surfaces is expected to occur(SRC). Methyl mercaptan is expected to volatilize rapidly from dry soil surfaces based upon its vapor pressure and because it is a gas a temperatures above 6 deg C(SRC). However, gaseous methyl mercaptan gas has been found to strongly adsorb to moist and dry soil surfaces suggesting that adsorption might be an environmental sink for methyl mercaptan(4). Therefore, the importance of volatilization from soil surfaces may be attenuated by adsorption(SRC).
Literature: (1) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, DC: Taylor and Francis (1989) (2) Hine J, Mookerjee PK; J Org Chem 40: 292-8 (1975) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (4) Smith KA et al; Soil Sci 116: 313-9 (1973)

Using a structure estimation method based on molecular connectivity indices(1), the Koc of methyl mercaptan can be estimated to be 13(SRC). According to a classification scheme(2), this estimated Koc value suggests that methyl mercaptan is expected to have very high mobility in soil. Gaseous methyl mercaptan has been observed to partition to soils(3). For example, when gaseous methyl mercaptan was passed over six air-dried and moist (50% field capacity) soils, 2.4-32.1 mg/g and 2.2-21.4 mg/g of methyl mercaptan rapidly adsorbed to the dry and moist soils, respectively(3). Neither the capacity or rate of sorption was correlated to soil pH, organic matter content, or clay content; sterile controls ruled out the involvement of microorganisms(3); it was suggested that adsorption to soil surfaces might be an environmental sink for gaseous methyl mercaptan(3).
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Jan, 2011. Available from, as of July 19, 2012: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Swann RL et al; Res Rev 85: 17-28 (1983) (3) Smith KA et al; Soil Sci 116: 313-9 (1973)

octylalcohol

KBPLFHHGFOOTCA-UHFFFAOYSA-N

caprylic alcohol

Heptyl carbinol

octanol

Octilin

Capryl alcohol

Octyl alcohol

octyl-alcohol

Primary octyl alcohol

1-Hydroxyoctane

1-hydroxyoctyl

n-Caprylic alcohol

N-octanol

Octyl alcohol normal-primary

AC1L1AEQ

n-Capryl alcohol

n-Heptyl carbinol

OC9

Alcohol C8

C8 alcohol

n-Octyl alcohol

N-octyl-alcohol

1-octanol

1-Oktanol

Lorol C8

Octyl alcohol, primary

Sipol L8

1-Octyl alcohol

2-Capryl alcohol

AC1Q2WB6

Alfol 8

EPAL 8

Octyl alcohol, normal-primary

Off-Shoot T

Off-shoot-T

Prim-n-octyl alcohol

SCHEMBL8822

1-Octanol, analytical standard

Alcohol C-8

Alcohol, C8

Fair 85

GTPL4278

KSC176Q9D

Lorol 20

CHEMBL26215

NSC9823

Octan-1-ol

Octyl alcohol (natural)

BDBM22606

c0045

CTK0H6891

Fatty alcohol(C8)

HMDB01183

HSDB 700

O0036

O0212

Octanol (all isomers)

WLN: Q8

Dytol M-83

RL00475

2-Octanol ~99%

bmse000970

bmse000980

C00756

C6-12 Alcohols

CCRIS 9099

Emery 3322

Emery 3324

HMS3039O07

n-Octan-1-ol

C6-C12 Alkyl alcohol

DTXSID7021940

FEMA Number 2800

LP064439

LP069551

LS-2996

NSC 9823

NSC-9823

octan-1-ol;

Octanol-(1)

OR000625

SBB059902

STL264193

UNII-6X61I5U3A4 component KBPLFHHGFOOTCA-UHFFFAOYSA-N

ACMC-2099b5

CHEBI:16188

DSSTox_CID_1940

ZINC1532735

AN-43095

ANW-16335

BP-21329

Caswell No. 456E

Caswell No. 611A

DSSTox_GSID_21940

EBD2203381

NV1779205D

TRA0009495

Alcohols, C6-12

DSSTox_RID_76416

LMFA05000130

MFCD00002988

AI3-02169

Lorol C 8-98

RTR-002327

ST51046170

TR-002327

UNII-NV1779205D

1-Octanol, ACS spectrophotometric grade, >=99%

AKOS000120100

EPA Pesticide Chemical Code 079029

EPA Pesticide Chemical Code 079037

J-002650

1-Octanol, anhydrous, >=99%

FEMA No. 2800

FT-0608179

MLS001055318

SMR000673567

I14-17870

(C6-C12) Alkyl alcohol

Tox21_201373

Tox21_300096

1-Octanol, ACS reagent, >=99%

111-87-5

F0001-0248

Mixed fatty alcohols (C6-C12)

Z1262253001

1-Octanol, for HPLC, >=99%

MCULE-2656577895

NCGC00091003-01

NCGC00091003-02

NCGC00091003-03

NCGC00091003-04

NCGC00091003-05

NCGC00254099-01

NCGC00258924-01

Octan-2-ol 98+ %

CAS-111-87-5

EINECS 203-917-6

EINECS 266-920-1

EINECS 271-642-9

1-Octanol, natural, >=98%, FCC

1-Octanol, ReagentPlus(R), 99%

12676-73-2

67700-96-3

68603-15-6

SDA 13-060-00

220713-26-8

1-Octanol, >=98%, FCC, FG

1-Octanol, 99% 500ml

MolPort-001-787-163

1-Octanol, JIS special grade, >=98.0%

1-Octanol, SAJ first grade, >=75.0%

1-Octanol, Vetec(TM) reagent grade, 98%

81301-EP2270018A1

81301-EP2272817A1

81301-EP2289891A2

81301-EP2305687A1

81301-EP2305825A1

81301-EP2380568A1

Alcohols, C8-18 and C18-unsatd.

103517-EP2270018A1

103517-EP2275416A1

103517-EP2287158A1

103517-EP2298313A1

103517-EP2301924A1

(C8-C18) and (C18) Unsaturatedalkyl alcohol

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

958E4752-AAC3-4F72-A0BF-02D95F9E8071

InChI=1/C8H18O/c1-2-3-4-5-6-7-8-9/h9H,2-8H2,1H

The Henry's Law constant for 1-octanol is reported as 2.5X10-5 atm-cu m/mole(1). This Henry's Law constant indicates that 1-octanol 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 43 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 17 days(SRC). 1-Octanol's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). 1-Octanol is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.0794 mm Hg(3).
Literature: (1) Yaws CL et al; Waste Manag 17: 541-7 (1997) (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; Data Compilation, Tables of Properties of Pure Cmpds, Design Inst for Phys Prop Data, Am Inst for Phys Prop Data, New York, NY (1989)

The Koc of 1-octanol is reported as 38(1). According to a classification scheme(2), this Koc value suggests that 1-octanol is expected to have very high mobility in soil(SRC).
Literature: (1) Schuumann G et al; Environ Sci Technol 40 :7005-11 (2006) (2) Swann RL et al; Res Rev 85: 17-28 (1983)

Monohydroxybenzene

hydroxybenzend

Hydroxybenzene

Hydroxybenzene solution

Carbolsaeure

Karbolsaeure

phenylalcohol

Benzophenol

Carbolsaure

Fenosmolin

Fenosmoline

MODIFIED POLYPHENYLENE ETHER

Monohydroxy benzene

Monophenol

Oxybenzene

Phenolcrude

Phenosmolin

Phylorinol

benzenod

Benzenol

Carbolicum acidum

Cepastat lozenges

ISWSIDIOOBJBQZ-UHFFFAOYSA-N

Phenol homopolymer

Phenol,industrial

Acide carbolique

Castellani Paint

Cepastat Cherry

CHLORASEPTIC SORE THROAT

Fenolo

Hydroxy-benzene

Liquefied phenol

Liquified Phenol

Liver Supplement

monophenyl ether

Pandy's reagent

Paoscle

Phenic

phenol

Phenol solution

Phenol solutions

Phenol synthetic

Phenolated water

Phenolated water for disinfection

Phenole

Phenyl hydroxide

Phenylic alcohol

Synthetic phenol

acide phenique

Campho-Phenique Liquid

carbolic acid

CEPASTAT EXTRA STRENGTH

Chloraseptic Sore Throat Cherry

Chloraseptic Sore Throat Citrus

Chloraseptic Sore Throat Menthol

Cuticura pain relieving ointment

Fenol

Izal

Liquid phenol

Phenic alcohol

Phenol alcohol

Phenol liquid

Phenol molten

PHENOL REAGENT

Phenyl alcohol

Phenyl hydrate

Phenylic acid

PhOH

Sore Throat Readyincase

TEA polyphenol

Throat Relief

Aseptil rojo

Carbolic acid liquid

Carbolic oil

EQUALINE SORE THROAT

IPH

Oral Relief

Phenic acid

Phenol polymer-bound

Sore Throat

Sterile Diluent for Allergenic Extract

Campho-Phenique Gel

Equate Sore Throat

HEALTHY ACCENTS SORE THROAT

Leader Sore Throat

Liquefied phenol BP

Phenol, sulfurated

Sore Throat Cherry

Sore Throat Menthol

Sunmark Sore Throat

Topcare Sore Throat

AC1L1AHZ

GOOD NEIGHBOR PHARMACY SORE THROAT

Phenol, detached crystals

Phenol, liquefied

Phenol, synthetic

Phenol, ultrapure

Sore Throat Relief Cherry

Sore Throat Relief Menthol

Sore Throat Spray

PHENOL REAGE NT

Phenol, liquid

Phenol, molten

Smart Sense Sore Throat

Sore Throat Relief Cherry Flavor

Sore Throat Spray Cherry

1ai7

1li2

4i7l

C6H6O

Carbolic acid, liquid

Dg Health Sore Throat

Good Sense Sore Throat

Phenol 6%

Phenol, polymer-bound

Phenol, pure

Phenol, solid

phenylic acid, phenyl hydroxide

Campho-Phenique Cold Sore Gel

Carbolsaure [German]

CARE ONE SORE THROAT

Eos Medicated Pain Relieving Lip Balm

Pain A Lay

PHENOL, ACS

Phenol, ACS reagent

Phenol, for molecular biology

ACMC-1CE2K

Benzene, hydroxy-

PHENOL, ULTRA PURE

Rx Act Sore Throat

3f39

AC1Q791G

Acide carbolique [French]

Baker's p and s

Fenolo [Italian]

Phenol (liquid)

Phenole [German]

WLN: QR

CHEMBL14060

CS0062

PHENOL- D6

UN1671

UN2312

UN2821

339NCG44TV

BDBM26187

Castellani Paint 1.5%

CCRIS 504

CTK0H5673

Fenol(DUTCH, POLISH)

H2391

HMDB00228

HSDB 113

Liquefied phenol (TN)

P1610

Paoscle (TN)

Phenol (TN)

Phenol [JAN]

Phenol, >=99%

(14C)Phenol

BIDD:ER0293

DB03255

LS-476

NSC36808

Phenol for disinfection (TN)

Phenol, 90% aqueous solution

RL00383

Baker's P and S Liquid and Ointment

bmse000290

bmse010026

C00146

C15584

D00033

LTBB002354

Phenol [USP:JAN]

Rcra waste number U188

UNII-339NCG44TV

AK113559

AM802906

DNC010455

DTXSID5021124

NA 2821

OR034257

OR192502

OR214349

OR214350

OR241808

OR251051

OR277357

OR285554

Phenol, pharmaceutical secondary standard; traceable to USP and PhEur

Phenol, United States Pharmacopeia (USP) Reference Standard

UN 1671

UN 2312

UN 2821

Baker's P & S liquid & Ointment

CHEBI:15882

DSSTox_CID_1124

Fenol [Dutch, Polish]

Liquefied phenol (JP17)

NCI-C50124

PHENOL, 80% in ethanol

Phenol, PESTANAL(R), analytical standard

PHENYL, 2-HYDROXY-

PHENYL, 4-HYDROXY-

ZINC5133329

AB1002201

AJ-53232

AN-22534

ANW-15995

BP-30160

DSSTox_GSID_21124

KB-59534

NSC 36808

NSC-36808

Phenol for disinfection (JP17)

Phenol, labeled with carbon-14

SC-26791

Caswell No. 649

DSSTox_RID_75955

MFCD00002143

MFCD03703209

Phenol, >=99.0%

Phenol, BP grade 80% aqueous solution

Phenol, unstabilized, purified by redistillation, >=99%

ZINC05133329

AI3-01814

LS-105199

Phenol (JP17/USP)

Phenol, LR, >=99%

RTR-002010

AKOS000119025

EPA Pesticide Chemical Code 064001

I01-9247

J-610001

RCRA waste no. U188

FEMA No. 3223

FT-0645154

FT-0673707

MLS001065591

SMR000568492

1,3-Butadiene,2-methyl-,homopolymer,phenol-modified

I14-62966

Liquified Phenol, meets USP testing specifications, >=89.0%

Tox21_113463

Tox21_201639

Tox21_300042

Un 2812 (solution)

108-95-2

F1908-0106

Phenol, natural, 97%, FG

Phenol, unstabilized, ReagentPlus(R), >=99%

UN 2312 (molten)

Phenol (or solutions with 5% or more phenol)

Phenol, AR, >=99.5%

UN 1671 (solid)

8002-07-1

MCULE-9943948107

NCGC00091454-01

NCGC00091454-02

NCGC00091454-03

NCGC00091454-04

NCGC00091454-05

NCGC00091454-06

NCGC00091454-07

NCGC00254019-01

NCGC00259188-01

Phenol, JIS special grade, >=99.0%

CAS-108-95-2

EINECS 203-632-7

EINECS 262-972-4

Phenol solution, certified reference material, 500 mug/mL in methanol

Phenol stock solution, 100 mg/dL, standard

Phenol, SAJ first grade, >=98.0%

14534-23-7

27073-41-2

50356-25-7

61788-41-8

63496-48-0

65996-83-0

68071-29-4

73607-76-8

84650-60-2

582-EP2269975A2

582-EP2269977A2

582-EP2269997A2

582-EP2270003A1

582-EP2270101A1

582-EP2270113A1

582-EP2272813A2

582-EP2272817A1

582-EP2272822A1

582-EP2272849A1

582-EP2272935A1

582-EP2272972A1

582-EP2272973A1

582-EP2274983A1

582-EP2275105A1

582-EP2275395A2

582-EP2275403A1

582-EP2275404A1

582-EP2275411A2

582-EP2275415A2

582-EP2275420A1

582-EP2277565A2

582-EP2277566A2

582-EP2277567A1

582-EP2277568A2

582-EP2277569A2

582-EP2277570A2

582-EP2277867A2

582-EP2277872A1

582-EP2277879A1

582-EP2277881A1

582-EP2279750A1

582-EP2280001A1

582-EP2280003A2

582-EP2280004A1

582-EP2280006A1

582-EP2280010A2

582-EP2280012A2

582-EP2280020A1

582-EP2280021A1

582-EP2281817A1

582-EP2281819A1

582-EP2284146A2

582-EP2284147A2

582-EP2284148A1

582-EP2284157A1

582-EP2284160A1

582-EP2284165A1

582-EP2284169A1

582-EP2284178A2

582-EP2286811A1

582-EP2286812A1

582-EP2287158A1

582-EP2287161A1

582-EP2287162A1

582-EP2287165A2

582-EP2287166A2

582-EP2287167A1

582-EP2289509A2

582-EP2289868A1

582-EP2289879A1

582-EP2289883A1

582-EP2289891A2

582-EP2289892A1

582-EP2289896A1

582-EP2289965A1

582-EP2292280A1

582-EP2292597A1

582-EP2292608A1

582-EP2292620A2

582-EP2295399A2

582-EP2295411A1

582-EP2295424A1

582-EP2295426A1

582-EP2295427A1

582-EP2295428A2

582-EP2295429A1

582-EP2295434A2

582-EP2295437A1

582-EP2295438A1

582-EP2298734A2

582-EP2298742A1

582-EP2298744A2

582-EP2298750A1

582-EP2298753A1

582-EP2298758A1

582-EP2298759A1

582-EP2298775A1

582-EP2298776A1

582-EP2298778A1

582-EP2301536A1

582-EP2301538A1

582-EP2301919A1

582-EP2301924A1

582-EP2301926A1

582-EP2301929A1

582-EP2301935A1

582-EP2301937A1

582-EP2301983A1

582-EP2302015A1

582-EP2305033A1

582-EP2305243A1

582-EP2305625A1

582-EP2305627A1

582-EP2305633A1

582-EP2305640A2

582-EP2305648A1

582-EP2305649A1

582-EP2305662A1

582-EP2305664A1

582-EP2305668A1

582-EP2305673A1

582-EP2305674A1

582-EP2305679A1

582-EP2305684A1

582-EP2305685A1

582-EP2305687A1

582-EP2305689A1

582-EP2305695A2

582-EP2305696A2

582-EP2305697A2

582-EP2305698A2

582-EP2305808A1

582-EP2308471A1

582-EP2308510A1

582-EP2308838A1

582-EP2308840A1

582-EP2308848A1

582-EP2308861A1

582-EP2308865A1

582-EP2308872A1

582-EP2308873A1

582-EP2308875A1

582-EP2308877A1

582-EP2308878A2

582-EP2308880A1

582-EP2311455A1

582-EP2311464A1

582-EP2311494A1

582-EP2311808A1

582-EP2311811A1

582-EP2311814A1

582-EP2311822A1

582-EP2311824A1

582-EP2311829A1

582-EP2311831A1

582-EP2311834A1

582-EP2314295A1

582-EP2314571A2

582-EP2314576A1

582-EP2314579A1

582-EP2314588A1

582-EP2315502A1

582-EP2316452A1

582-EP2316470A2

582-EP2316824A1

582-EP2316829A1

582-EP2316831A1

582-EP2316832A1

582-EP2316833A1

582-EP2316836A1

582-EP2316937A1

582-EP2316974A1

582-EP2371806A1

582-EP2371807A1

582-EP2371811A2

582-EP2372017A1

582-EP2374784A1

582-EP2374785A1

582-EP2377842A1

582-EP2380872A1

Phenol solution, 5000 mug/mL in methanol, certified reference material

Phenol solutions [UN2821] [Poison]

Tox21_113463_1

Phenol, detached crystals, 99% 100g

MolPort-000-871-946

139-02-6 (hydrochloride salt)

78049-EP2272846A1

78049-EP2277868A1

78049-EP2277869A1

78049-EP2277870A1

78049-EP2287158A1

78049-EP2292608A1

78049-EP2308866A1

78049-EP2371806A1

78049-EP2371807A1

97694-EP2305662A1

Phenol solutions [UN2821] [Poison]

Phenol, BioXtra, >=99.5% (GC)

Phenol, contains hypophosphorous as stabilizer, loose crystals, ACS reagent, >=99.0%

Phenol, molten [UN2312] [Poison]

Phenol, for molecular biology, ~90% (T), liquid

Phenol, solid [UN1671] [Poison]

Phenol solution, 100 mug/mL in acetonitrile, PESTANAL(R), analytical standard

Phenol, molten [UN2312] [Poison]

Phenol, BioUltra, for molecular biology, >=99.5% (GC)

Phenol, solid [UN1671] [Poison]

Phenol, BioUltra, for molecular biology, TE-saturated, ~73% (T)

Phenol, >=96.0% (calc. on dry substance, T)

Phenol solution, Equilibrated with 10??mM Tris HCl, pH??8.0, 1??mM EDTA, BioReagent, for molecular biology

Phenol, p.a., ACS reagent, 99.5-100.5%

p-Hydroxy polystyrene (100-200 mesh, 0.5-1.5 mmol/g)

InChI=1/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7

Phenol solution, BioReagent, Saturated with 0.1 M citrate buffer, pH??4.3 +/- 0.2, for molecular biology

Phenol, puriss., meets analytical specification of Ph. Eur., BP, USP, >=99.5% (GC), crystalline (detached)

Phenol, puriss. p.a., ACS reagent, reag. Ph. Eur., 99.0-100.5%

Phenol, puriss., meets analytical specification of Ph. Eur., BP, USP, 99.5-100.5% (GC)

Phenol, polymer-bound, 100-200 mesh, extent of labeling: 0.5-1.5 mmol/g loading, 1 % cross-linked with divinylbenzene

The Henry's Law constant for phenol is 3.33X10-7 atm-cu m/mol at 25 deg C(1). This Henry's Law constant indicates that phenol is expected to be essentially nonvolatile from water surfaces(2). Phenols's Henry's Law constant indicates that volatilization from moist soil surfaces in not expected to occur(SRC). Phenol is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.35 mm Hg(3).
Literature: (1) Gaffney JS et al; Environ Sci Technol 21: 519-23 (1987))(2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Bingham E et al, eds; Patty's Toxicology. 5th ed. NY, NY: John Wiley & Sons Inc. 4: 383 (2001)

Phenol is reported to have low adsorptivity to clay soils and silt loam(1) and no adsorption to aquifer material(3) and montmorillonite and kaolinite clays(8). The Koc for phenol to a Batcombe silt loam soil (pH 6.7, organic carbon 2.51%) was 30(6). It was 16 for a Brookstone clay loam (pH 5.7, organic matter 5.1%) and varied with pH and iron content of the soil(7). The Freundlich K and (1/N) for phenol in Captina (pH 5.7, 1.1 % organic matter) and Palouse silt loam (pH 5.7, 3.6% organic matter) soils were 0.58 (1.15) and 0.81 (1.00)(2); the Koc values for these soils are 91 and 39(SRC). Based on the reported Koc values, phenol would be expected to generally exhibit very high mobility in soil, based on a classification scheme(4). In a study of the adsorption of phenol onto siltstone associated with a Wyoming coal deposit suitable for in situ gasification, the pH of the solution was the major controlling factor with adsorption occurring at pH's below the pKa of phenol and no adsorption occurring at pH's above the pKa(5). The log of the Freundlich K value was approximately -4(5). Therefore, phenol may be transported by groundwater near in situ coal gasification sites due to the elevated pH's at these sites after gasification(5). The pKa of phenol is 9.99(9), indicating that it will be partially dissociated at the upper end of environmental pH range and its mobility may be pH dependent(SRC). In general, anions generally do not adsorb to organic carbon and clay as strongly as their neutral counterparts(10).
Literature: (1) Artiola-Fortuny J, Fuller WH; Soil Sci 133: 18-26 (1982) (2) Scott HD et al; J Environ Qual 12: 91-5 (1983) (3) Ehrlich GG et al; Groundwater 20: 703-10 (1982) (4) Swann RL et al; Res Rev 85: 17-28 (1983) (5) Laquer FC, Manahan SE; Chemosphere 16: 1431-45 (1987) (6) Briggs GG; J Agric Food Chem 29: 1050-9 (1981) (7) Boyd SA et al; Appl Environ Microbiol 46: 50-4 (1983) (8) Luh MD, Baker RA; pp. 534-42 in Proc 25th Ind Waste Conf Purdue Univ (1970) (9) Lide DR, ed; CRC Handbook of Chemistry and Physics. 81st Ed. Boca Raton, FL: CRC Press LLC, p. 5-89 (2000) (10) Doucette WJ; pp. 141-188 in Handbook of Property Estimation Methods for Chemicals. Boethling RS, Mackay D, eds. Boca Raton, FL: Lewis Publ (2000)

Isobutylcarbinol

isopentylalcohol

Isopentylalkohol

ISOAMYLALCOHOL

Isopentanol

Alcool isoamylique

Fuseloel

Isoamylol

Isobutyl carbinol

Isopentyl alcohol

PHTQWCKDNZKARW-UHFFFAOYSA-N

Amylowy alkohol

Fermentation amyl alcohol

Iso-amylalkohol

Isoamyl alcohol

Isoamyl alkohol

isoamyl-alcohol

Alcool amilico

Primary isoamyl alcohol

3-methylbutanoI

3-Methylbutanol

Fusel Oil

AC1Q7CHF

Iso-amyl alcohol

potato-spirit oil

ACMC-1ADLL

Huile de fusel

i-Amyl Alcohol

Isoamyl alcohol, primary

3-Methylbutanol, analytical standard

DEM9NIT1J4

3-methyl butanol

3-methyl-Butanol

3-Metil-butanolo

AC1L1L9D

AC1Q1PG0

ISOAMYL ALCOHOL, ACS

Alcool isoamylique [French]

isopentan-1-ol

UNII-DEM9NIT1J4

Alcool amilico [Italian]

Amylowy alkohol [Polish]

Iso-amylalkohol [German]

Isoamyl alcohol (natural)

KSC175S7D

1-Hydroxy-3-Methylbutane

7340AF

Isoamyl alkohol [Czech]

NATURAL ISOAMYL ALCOHOL - TECHNICAL GRADE

NSC1029

NSC7905

CTK0H5971

HMDB06007

HSDB 605

I0289

Isoamyl alcohol (primary and secondary)

NATURAL ISOAMYL ALCOHOL P & F

QSPL 002

3-methylbutane-1-ol

CHEMBL372396

DB02296

Isopentyl alcohol (8CI)

2-Methyl-4-butanol

3-methyl 1-butanol

3-Methyl-1-butanol

3-Methylbutan-1-ol

C07328

CCRIS 8806

ZINC896830

DTXSID3025469

FEMA Number 2057

Jsp001579

LP092178

LS-2837

NSC 1029

NSC-1029

NSC-7905

OR034211

OR210114

STL282718

UNII-2NK7O363Q6 component PHTQWCKDNZKARW-UHFFFAOYSA-N

ZB015111

3-Metil-butanolo [Italian]

Butanol, 3-methyl-

CHEBI:15837

DSSTox_CID_5469

3-Methyl-1-butanol, analytical standard

AN-22920

ANW-18132

DSSTox_GSID_25469

Isoamyl alcohol (3-methyl butanol)

KB-70935

3-Methyl-Butan-1-Ol

DSSTox_RID_77799

LMFA05000108

Magnesium bis(3-methylbutan-1-olate)

Methyl-3-butan-1-ol

MFCD00002934

ZINC00896830

AI3-15288

Isoamyl alcohol, >=98%, FG

RTR-003692

TR-003692

3-METHYL-1-BUTANOL, REAG

AKOS000118739

FEMA No. 2057

FT-0616032

TRA-0206228

1-Butanol, 3-methyl-

3-Methyl-1-butanol, mixture of isomers

Butan-1-ol, 3-methyl

I14-14690

Z955123582

Isoamyl alcohol, natural, >=98%, FG

Tox21_302359

WLN: Q2Y1 & 1

123-51-3

F0001-0367

3-Methyl-1-butanol, 98%

3-METHYL-BUTAN-(1)-OL

6423-06-9

MCULE-7411270401

NCGC00255329-01

CAS-123-51-3

EINECS 204-633-5

EINECS 229-179-5

3-Methyl-1-butanol, anhydrous, >=99%

3-Methyl-1-butanol, United States Pharmacopeia (USP) Reference Standard

3-Methyl-1-butanol, technical grade, 95%

3-Methylbutanol, BioReagent, for molecular biology, >=98.5%

1973-EP2281899A2

1973-EP2316937A1

3-Methyl-1-butanol, LR, >=98%

3-Methyl-1-butanol, reagent grade, 98%

MolPort-001-793-103

123-51-3 (Parent)

74374-EP2269986A1

74374-EP2308857A1

74374-EP2380568A1

3-Methyl-1-butanol, biotech. grade, >=99%

3-Methyl-1-butanol, ReagentPlus(R), >=99%

117932-EP2287147A2

117932-EP2298768A1

6423-06-9 (magnesium salt)

3-Methyl-1-butanol, ACS reagent, >=98.5%

3-Methyl-1-butanol, JIS special grade, >=98.0%

3-Methyl-1-butanol, SAJ first grade, >=96.0%

3-Methylbutanol, BioUltra, for molecular biology, >=99.0% (GC)

3-Methyl-1-butanol, p.a., 99.8%

3-Methyl-1-butanol, ACS, 98.5% min. 500ml

3-Methylbutanol, puriss. p.a., ACS reagent, >=98.5% (GC)

3-Methylbutanol, p.a., ACS reagent, reag. ISO, reag. Ph. Eur., 98.5%

InChI=1/C5H12O/c1-5(2)3-4-6/h5-6H,3-4H2,1-2H

The Henry's Law constant for isopentanol is 1.41X10-5 atm-cu m/mol(1). Using this value for the Henry's Law constant, one can estimate that the volatilization half-life of isopentanol in a model river 1 m deep flowing at 1 m/s with a wind speed of 3 m/s is 2.55 days(2). Similarly, the half-life of isopentanol in a model lake 1 m deep with a 0.05 m/s current and a 0.5 m/s wind is 21 days(2). In view of isopentanol's relatively high vapor pressure, 2.37 mm Hg at 25 deg C(3) and moderate Henry's Law constant and low adsorptivity to soil, isopentanol would be expected to volatilize from dry and moist soil(SRC).
Literature: (1) Butler JAV et al; J Chem Soc 1935: 280-5 (1935) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. NY: McGraw-Hill Chapt 15 (1982) (3) Riddick JA et al; Organic Solvents 4th ed; pp. 221-2 NY: Wiley (1986)

The Koc for isopentanol estimated from its water solubility, 26.7 mg/L(1), using recommended regression equations are 720(2) and 679(4). However, the chemicals used in developing these equations were mainly pesticides and their structures are not similar to isopentanol. The Koc for isopentanol estimated from molecular structure is 4(3). This should be a reasonable estimate for the Koc because it is close to the experimental value for the structurally similar chemical, 1-pentanol, 1.6(6). According to a suggested classification scheme(5), the estimated Kocs based on molecular structure suggests that isopentanol is very highly mobile in soil(SRC).
Literature: (1) Riddick JA et al; Organic Solvents 4th ed; pp. 211-2 NY: Wiley (1986) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. NY: McGraw-Hill Chapt 4 (1982) (3) Meylan WM et al; Environ Sci Technol 26: 1560-7 (1992) (4) Wauchope RD et al; Rev Environ Contam Toxicol 123: 1-155 (1991) (5) Swann RL et al; Res Rev 85: 17-28 (1983) (6) Gerstl Z, Helling CS; J Environ Sci Health B22: 55-69 (1987)