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)

Capronaldehyde

Caproaldehyde

Hexanaldehyde

Hexylaldehyde

Kapronaldehyd

Hexaldehyde

JARKCYVAAOWBJS-UHFFFAOYSA-N

n-Caproylaldehyde

Caproic aldehyde

HEXANAL

Hexoic aldehyde

n-Caproaldehyde

n-Capronaldehyde

n-Hexylaldehyde

Hexyl aldehyde

n-Hexaldehyde

Caproaldehyde, Hexyl aldehyde

Hexanal, analytical standard

n-Caproic aldehyde

n-Hexanal

AC1Q2VPQ

1-hexanone

6-OXOHEXYL

Aldehyde C6

C6 aldehyde

1-Hexanal

Kapronaldehyd [Czech]

AC1L1LZ0

9DC2K31JJQ

ACMC-1BFR4

Aldehydes, C6

C6H12O

Hexanal (natural)

PubChem3077

Aldehyde C-6

E-2-hexanal

KSC353M9N

7134AH

hexan-1-al

n-C5H11CHO

NSC2596

SCHEMBL22263

UN1207

UNII-9DC2K31JJQ

CTK2F3696

Hexanal, 98%

HMDB05994

HSDB 560

WLN: VH5

CHEMBL280331

NE10466

RP18712

CCRIS 3219

n-HEXALDEHYDE, 98%

DTXSID2021604

FEMA Number 2557

LP094954

LP104070

LS-2339

NSC 2596

NSC-2596

OR012182

STL280331

UN 1207

A835388

CHEBI:88528

DSSTox_CID_1604

ZINC1641021

AN-23753

ANW-35172

CJ-05867

CJ-26448

DSSTox_GSID_21604

EBD3061058

SC-06151

BDBM50028824

DSSTox_RID_76231

LMFA06000109

MFCD00007027

ZINC01641021

AI3-15364

DB-054893

RTR-022440

TR-022440

AKOS009156478

J-660017

S14-1025

BRN 0506198

FEMA No. 2557

FT-0631290

FT-0669191

TRA-0203532

66-25-1

EN300-33498

Hexanal, natural, >=90%, FG

Hexanal, natural, >=95%, FG

Tox21_201933

Tox21_303342

CAS-66-25-1

Hexanal, >=97%, FCC, FG

Hexaldehyde [UN1207] [Flammable liquid]

NCGC00249137-01

NCGC00257270-01

NCGC00259482-01

EINECS 200-624-5

EC 200-624-5

Hexaldehyde [UN1207] [Flammable liquid]

MolPort-001-769-760

4-01-00-03296 (Beilstein Handbook Reference)

The Henry's Law constant for hexaldehyde is 2.13X10-4 atm-cu m/mole(1). This Henry's Law constant indicates that hexaldehyde 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 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)(2) is estimated as 5 days(SRC). Hexaldehyde's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Hexaldehyde is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 11.3 mm Hg(3).
Literature: (1) Buttery RG et al; J Agric Food Chem 17: 385-9 (1969) (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 hexaldehyde is estimated as 50(SRC), using a log Kow of 1.78(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that hexaldehyde 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. 24 (1995) (2) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Nov, 2012. Available from, as of May 18, 2015: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (3) Swann RL et al; Res Rev 85: 17-28 (1983)

Phosphosulfurized alpha-pinene

ALPHA-PINENEPOLYMER

alphapinene

GRWFGVWFFZKLTI-UHFFFAOYSA-N

Cyclic dexadiene

alpha-Pinene, phosphosulfurized

Pinene isomer

alpha pinene

ALPHA-PINENE

Sylvapine A

Acintene A

Acitene A

Wilt Pruf

Alpha Pinene PF

DL-ALPHA-PINENE

2-Pinene

PINENE, ALPHA

1R-alpha-Pinene

AC1L1N0D

alpha-pinene, pinene

alpha-Pinene(dextro)

1R-a-Pinene

.alpha.-Pinene

alpha-Pinene (natural)

NSC7727

pin-2-ene

UN2368

CCRIS 697

CTK5E7908

HMDB06525

HSDB 720

CHEMBL442565

NSC94522

NSC94523

PC 500

alpha [D] Pinene

alpha [L] Pinene

C09880

BT000143

DTXSID4026501

FEMA Number 2902

LS-2348

NSC 7727

NSC-7727

OR038360

OR246844

OR249294

Pinene, .alpha.

SBB060477

UN 2368

1R-.alpha.-Pinene

1S-.alpha.-Pinene

CHEBI:36740

DSSTox_CID_6501

AN-19420

AN-19426

AN-42193

DSSTox_GSID_26501

NSC-94522

NSC-94523

SC-18193

DSSTox_RID_78126

PINENE, ALPHA (D)

PINENE, ALPHA (L)

AI3-24594

ST51046656

AKOS000121239

Q-201582

(+)-a-Pinene

BRN 3194807

FEMA No. 2902

FT-0604379

FT-0604414

FT-0622197

FT-0698080

pin-2(3)-ene

(R)-.alpha.-Pinene

80-56-8

(+-)-alpha-pinene

Tox21_110996

Tox21_200108

Tox21_303385

1R-(+)-alpha-pinene

alpha-Pinene, phosphorus pentasulfide reaction product (4:1)

DL-Pin-2(3)-ene

CAS-80-56-8

1R-(+)-a-pinene

MCULE-3589656574

NCGC00090682-01

NCGC00090682-02

NCGC00257379-01

NCGC00257662-01

(+-)-2-pinene

(+/-)-alpha-Pinene

EINECS 201-291-9

EINECS 219-445-9

EINECS 267-032-7

25766-18-1

39388-04-0

39423-40-0

50815-61-7

53569-35-0

56833-58-0

57762-87-5

67762-73-6

68411-25-6

72510-05-5

102640-64-2

103657-08-5

459844-87-2

alpha-Pinene [UN2368] [Flammable liquid]

(+/-)-2-Pinene

MolPort-003-926-536

(1R)-(+)-a-Pinene

(+)-Pin-2(3)-ene

2,6-Trimethylbicyclo[3.1.1]-2-heptene

(.+/-.)-.alpha.-Pinene

2,6,6-Trimethylbicyclo(3.1.1)hept-2-ene

2,6,6-Trimethylbicyclo[3.1.1]-2-heptene

2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene

4,6,6-trimethylbicyclo[3.1.1]hept-3-ene

4,6,6-Trimethylbicyklo(3,1,1)hept-3-en

Bicyclo[3.1.1]hept-2-ene,6,6-trimethyl-

2,6-Trimethylbicyclo[3.1.1]-2-hept-2-ene

2,6,6-trimethyl-Bicyclo(3.1.1)hept-2-ene

2,6,6-trimethyl-bicyclo[3.1.1]hept-2-ene

2-Pinene, (1S,5S)-(-)-

2,6,6-Trimethyl bicyclo-(3,1,1)-2 heptene

Bicyclo(3.1.1)hept-2-ene, 2,6,6-trimethyl

Bicyclo[3.1.1]hept-2-ene,2,6,6-trimethyl-

2,6,6-Trimethylbicyclo(3.1.1)-2-hept-2-ene

4,6,6-Trimethylbicyklo(3,1,1)hept-3-en [Czech]

Bicyclo(3.1.1)hept-2-ene, 2,6,6-trimethyl-, phosphosulfurized

Bicyclo(3.1.1)hept-2-ene, 2,6,6-trimethyl-

Bicyclo[3.1.1]hept-2-ene, 2,6,6-trimethyl-

(1R)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene

(1S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene

Bicyclo(3.1.1)hept-2-ene, 2,6,6-trimethyl-, homopolymer

Bicyclo[3.1.1]hept-2-ene, 2,6,6-trimethyl-, (1R)-

Bicyclo[3.1.1]hept-2-ene, 2,6,6-trimethyl-, (1S)-

Bicyclo[3.1.1]hept-2-ene, 2,6,6-trimethyl-, (.+/-.)-

The Henry's Law constant for alpha-pinene is estimated as 0.29 atm-cu m/mole(SRC) derived from its vapor pressure, 4.75 mm Hg(1), and water solubility, 2.49 mg/L(2). This Henry's Law constant indicates that alpha-pinene 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 3 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 5 days(SRC). alpha-Pinene's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of alpha-pinene from dry soil surfaces may exist based upon a vapor pressure of 4.75 mm Hg(1).
Literature: (1) 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 (1989) (2) Li J, Perdue EM; Physicochemical properties of selected monoterpenes. Pre-print extended abstract, Presented before the Division of Environmental Chemistry, Amer. Chem. Soc., Anaheim, CA, April 2-7, 1995 (1995) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)

ALMOST INSOLUBLE IN PROPYLENE GLYCOL & GLYCERINE
Literature: Fenaroli's Handbook of Flavor Ingredients. Volume 2. Edited, translated, and revised by T.E. Furia and N. Bellanca. 2nd ed. Cleveland: The Chemical Rubber Co., 1975., p. 486
Literature: #Sol in alcohol, chloroform, ether, glacial acetic acid, fixed oils
Literature: Lewis, R.J. Sax's Dangerous Properties of Industrial Materials. 10th ed. Volumes 1-3 New York, NY: John Wiley & Sons Inc., 1999., p. 2970
Literature: #In water, 2.49 mg/L at 25 deg C
Literature: Li J, Perdue EM; Physicochemical Properties of Selected Monoterpenes. Pre-print Extended Abstract, Presented Before The Division of Environmental Chemistry, Amer Chem Soc, Anaheim, Ca: April 2-7 (1995)

The Koc of alpha-pinene is estimated as 2,600(SRC), using a water solubility of 2.49 mg/L(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that alpha-pinene is expected to have slight mobility in soil.
Literature: (1) Li J, Perdue EM; Physicochemical properties of selected monoterpenes. Pre-print extended abstract, Presented before the Division of Environmental Chemistry, Amer. Chem. Soc., Anaheim, CA, April 2-7, 1995 (1995) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 4-5 (1990) (3) Swann RL et al; Res Rev 85: 17-28 (1983)

Methylethylacetaldehyde

alpha-Methylbutyraldehyde

alpha-Methylbutyric aldehyde

alpha-Methylbutanal

BYGQBDHUGHBGMD-UHFFFAOYSA-N

Methyl ethyl acetaldehyde

2-Methylbutyraldehyde

.alpha.-Methylbutyraldehyde

2-Methylbutyric aldehyde

2-Methylbutyraldehyde, analytical standard

2-METHYLBUTANAL

2-Formylbutane

2-Ethylpropanal

2-methyl butyraldehyde

Acetaldehyde, ethylmethyl-

2-methyl-butyraldehyde

S-2-METHYLBUTANAL

Nat.2-Methyl Butyraldehyde

.alpha.-Methylbutanal

.alpha.-Methylbutyric aldehyde

sec-C4H9CHO

AC1L1OF7

2-Methyl-Butanal

2-Methylbutyraldehyde (natural)

KSC202Q5N

AC1Q2S32

CTK1A2856

2- ethyl propanal

2-Methylbutyraldehyde, 95%

alpha-2-Methyl-n-butanal

WLN: VHY2&1

NSC77077

Butyraldehyde, 2-methyl-

ACMC-209s6n

2-Methyl-1-butanal

C02223

CCRIS 2944

2-methylbutan-1-al

LS-2912

OR010846

OR231043

OR258853

DTXSID2021818

CHEMBL2270060

DSSTox_CID_1818

CHEBI:16182

Butanal, 2-methyl-

ANW-40797

DSSTox_GSID_21818

2-Methylbutyraldehyde, natural, 98%

NSC 77077

KB-25099

NSC-77077

AN-24338

MFCD00006984

DSSTox_RID_76346

2-Methylbutyraldehyde, >=95%, FG

TR-032175

AI3-33276

RTR-032175

DB-057627

AKOS009107038

FEMA No. 2691

BRN 1633540

FT-0613025

I14-49148

96-17-3

Tox21_201242

Tox21_302866

CAS-96-17-3

NCGC00258794-01

NCGC00256324-01

NCGC00249003-01

EINECS 202-485-6

57456-98-1

MolPort-001-786-891

(.+/-.)-2-Methylbutanal

Butanal, 2-methyl-, (2R)-

3-01-00-02813 (Beilstein Handbook Reference)

gammabutyrolactone

gamma-Hydroxybutyrolactone

BUTYROLACTONE

butyrolactonL

Butyrylactone

gamma Butyrolactone

gamma-Butanolactone

gamma-Butyrolactone

gamma-Butyryllactone

Hydroxybutanoic Acid Lactone

sigma-Butyrolactone

gama-Butyrolactone

gamma-Butalactone

YEJRWHAVMIAJKC-UHFFFAOYSA-N

2-Oxotetrahydrofuran

Butyryl lactone

g-Butyrolactone

g-Butyryllactone

gamma-Hydroxybutyric acid lactone

gamma-hydroxybutyric acid lactonL

y-Butyrolactone

Agrisynth BLO

BLON

butyrl lactone

g-Butalactone

gamma-Butyrolactone, analytical standard

4-Deoxytetronate

BLO

Butyric acid lactone

g-Hydroxybutyric acid lactone

gamma-butyro-lactone

gamma-Hydroxybutyric Acid cyclic ester

GBL

.gamma.-Hydroxybutyrolactone

4-butanolactone

4-Butyrolactone

4-butyrolactonL

4-Butanolide

4-Hydroxybutanoic acid lactone

AC1L1OGM

AC1Q6EQU

gamma BL

gamma-BL

Tetrahydro-2-furanone

tetrahydrofuran-2-one

2-Oxolanone

4-Deoxytetronic acid

4-Hydroxybutyric acid lactone

4-hydroxybutyric acid lactonL

No Go

.alpha.-Butyrolactone

.gamma.-Butanolactone

.gamma.-Butyrolactone

4-hydroxybutyric acid gamma-lactone

Dihydro-2-furanone

dihydrofuran-2-one

Dihyro-2-furanone

gamm a-hydroxybutyric acid cyclic ester

Gamma-Lactone 4-hydroxybutanoic acid

Gamma-Lactone 4-hydroxybutyric acid

Paint Clean G

gamma-Butyrolactone (natural)

.gamma.-Hydrooxybutyric acid lactone

.gamma.-Hydroxybutyric acid lactone

OL659KIY4X

1,4-Butyrolactone

GTPL5462

KSC492Q2B

oxolan-2-one

WLN: T5OVTJ

.gamma.-Hydroxybutyric acid cyclic ester

1-Oxacyclopentane-2-one

1,2-Butanolide

1,4-Butanolide

4-Hydroxybutyric acid, gamma-lactone

CHEMBL95681

dihydro-furan-2-one

Gamma-Lactone 4-hydroxy-butanoic acid

Gamma-Lactone 4-hydroxy-butyric acid

NSC4592

PubChem17411

UNII-OL659KIY4X

1-Oxacyclopentan-2-one

2(3H)-dihydrofuranone

A4867

and oxolan-2-one

B0767

CTK3J2820

HMDB00549

.gamma.-BL

1,4-Lactone

1,4-lactonL

4-hydroxy-Butanoic acid g-lactone

DB04699

EBD36709

LS40356

RP18446

C01770

CCRIS 2924

DSSTox_CID_224

gamma-6480

HSDB 4290

LTBB001793

AK116990

DTXSID6020224

HE027248

HE261495

HE261496

HE388064

HE419942

LS-2010

NSC 4592

NSC-4592

STL281877

ACMC-209s75

Butanoic acid, .gamma.-lactone

BUTANOIC ACID,4-HYDROXY,LACTONE GAMMA-BUTYROLACTONE

C-1070

CHEBI:42639

Dihydro-2(3H)-furanone

dihydrofuran-2(3H)-one

NCI-C55878

ZINC4658567

AJ-51844

AN-24351

ANW-40815

Butyric acid, .gamma.-lactone

Caswell No. 132B

DSSTox_GSID_20224

SC-18055

TRA0048639

DSSTox_RID_75445

LMFA07040004

ZINC04658567

4-Hydroxybutanoic acid, .gamma.-lactone

4-Hydroxybutyric acid, .gamma.-lactone

AI3-28121

KB-251543

RTR-032131

TR-032131

AKOS000119924

EPA Pesticide Chemical Code 122303

gamma-Butyrolactone, ReagentPlus(R), >=99%

I14-6510

J-513020

J-520327

Q-200482

endo-cis-5-Norbornene-endo-2,3-dicarboxylic anhydride

FEMA No. 3291

FT-0622894

FT-0658293

gamma-Butyrolactone, >=99% (GC)

Tetrahydro-2-Furanone Dihydro-2(3H)-Furanone

.gamma.-6480

96-48-0

Dynasolve 699 (Salt/Mix)

Butanoic acid, 4-hydroxy-, gamma-lactone

Butyric acid, 4-hydroxy-, gamma-lactone

Tox21_200490

Tox21_300188

2(3H)-Furanone, dihydro-

3B1-008035

F0001-2298

CAS-96-48-0

gamma-Butyrolactone, SAJ first grade, >=99.5%

MCULE-6795890265

NCGC00247920-01

NCGC00247920-02

NCGC00253913-01

NCGC00258044-01

EINECS 202-509-5

4,5-Dihydro-2(3H)-furanone

Dihydro-(3 H)-furan-2-one

2,3,4,5-Tetrahydro-2-furanone

4-Hydroxybutanoic acid lactone, >=98%, FCC, FG

187997-16-6

Butanoic acid, 4-hydroxy-, .gamma.-lactone

Butyric acid, 4-hydroxy-, .gamma.-lactone

33522-EP2311815A1

33522-EP2371797A1

33522-EP2371798A1

33522-EP2371804A1

80109-EP2272517A1

80109-EP2277871A1

80109-EP2292621A1

80109-EP2305250A1

80109-EP2371797A1

80109-EP2371800A1

gamma-Butyrolactone, puriss., >=99.0% (GC)

4-Hydroxybutyric acid gamma-lactone; BLO; endo-cis-5-Norbornene-endo-2,3-dicarboxylic anhydride

InChI=1/C4H6O2/c5-4-2-1-3-6-4/h1-3H

The Henry's Law constant for butyrolactone is estimated as 5.3X10-8 atm-cu m/mole(SRC) derived from its vapor pressure, 0.45 mm Hg(1), and assigned value for water solubility of 1X10+6 mg/L (miscible)(2). This Henry's Law constant indicates that butyrolactone is expected to be essentially nonvolatile from water surfaces(3). Butyrolactone's estimated Henry's Law constant indicates that volatilization from moist soil surfaces is not likely to occur(SRC). Butyrolactone is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure of 0.45 mm Hg(1).
Literature: (1) Yaws CL; Handbook of Chemical Compound Data for Process Safety p. 35 (1997) (2) O'Neil MJ, ed; The Merck Index. 14th ed. Whitehouse Station, NJ: Merck and Co., Inc. pp. 259-60 (2006) (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 butyrolactone is estimated as 11(SRC), using a log Kow of -0.64(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that butyrolactone is expected to have very 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. 9 (1995) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc p. 4-9 (1990) (3) Swann RL et al; Res Rev 85: 17-28 (1983)

Ethylhexanol

YIWUKEYIRIRTPP-UHFFFAOYSA-N

2-ethylhexylalcohol

2 Ethylhexanol

2-Aethylhexanol

2-Ethylhexanol

AC1L1PEC

2-Ethylhexyl alcohol

Exxal 8N

2-ETHYL HEXANOL

2-ethyl-hexanol

AC1Q2V9L

AC1Q7BK8

2-ethyl hexyl alcohol

Alcohol, 2-ethylhexyl

KSC175S7B

L260

ACMC-1B65F

ACMC-20msz8

CHEMBL31637

NSC9300

SCHEMBL16324

CTK0H5970

E0122

Ethylhexanol, 2-

2-Aethylhexanol [German]

LS-380

2-ethyl 1-hexanol

2-ETHYL-1-HEXANOL

2-Ethylhexan-1-ol

C02498

CCRIS 2292

DSSTox_CID_605

HMS2268N10

HSDB 1118

AK114196

DTXSID5020605

LP121394

NSC 9300

NSC-9300

OR025415

SBB059906

STL453673

CHEBI:16011

2-Ethyl-1-hexanol, analytical standard

ANW-15107

DSSTox_GSID_20605

TRA0052020

xi-2-Ethyl-1-hexanol

2-Ethyl-hexan-1-ol

DSSTox_RID_75686

LMFA05000703

MFCD00004746

AI3-00940

KB-170355

RTR-001032

ST24040552

ST51046173

TR-001032

AKOS000120105

AKOS016843836

W-109057

BRN 1719280

FEMA No. 3151

FT-0612231

FT-0627437

MLS002415694

SMR000112222

1-Hexanol, 2-ethyl-

I14-17807

Tox21_202071

Tox21_300019

WLN: Q1Y4 & 2

104-76-7

3B1-005666

2-Ethyl-1-hexanol, >=99%

MCULE-1768780358

NCGC00091294-01

NCGC00091294-02

NCGC00091294-03

NCGC00254215-01

NCGC00259620-01

Alcohols, C7-9-branched, C8-rich

CAS-104-76-7

EINECS 203-234-3

EINECS 295-250-2

2-Ethylhexan-1-ol, United States Pharmacopeia (USP) Reference Standard

91994-92-2

111675-57-1

128821-84-1

Alcohols, C7-9-iso-,C8-rich

2-Ethyl-1-hexanol, >=99.6%

MolPort-001-787-201

2-Ethyl-1-hexanol, >=99%, FG

33017-EP2305033A1

33017-EP2311815A1

33017-EP2371805A1

33017-EP2377844A2

2-Ethyl-1-hexanol, 99% 500ml

2-Ethyl-1-hexanol, SAJ first grade, >=99.0%

1-Hexanol, 2-ethyl-, (S)-

4-01-00-01783 (Beilstein Handbook Reference)

1070-10-6 (titanium(4+) salt)

2-Ethyl-1-hexanol, puriss., >=99.0% (GC)

InChI=1/C8H18O/c1-3-5-6-8(4-2)7-9/h8-9H,3-7H2,1-2H

The Henry's Law constant for 2-ethylhexanol is estimated as 2.6X10-5 atm-cu m/mole(SRC) derived from its vapor pressure, 0.136 mm Hg(1), and water solubility, 880 mg/L(2). This Henry's Law constant indicates that 2-ethylhexanol is expected to volatilize 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 41 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 16 days(SRC). 2-Ethylhexanol's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). 2-Ethylhexanol is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(1).
Literature: (1) Daubert TE, Danner RP; Data Compilation Tables of Properties of Pure Compounds. New York, NY: Amer Inst for Phys Prop Data (1989) (2) Amidon GL et al; J Pharm Sci 63: 1858-66 (1974) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)

Using a structure estimation method based on molecular connectivity indices(1), the Koc of 2-ethylhexanol can be estimated to be 35(SRC). According to a classification scheme(2), this estimated Koc value suggests that 2-ethylhexanol 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 Feb 5, 2014: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Swann RL et al; Res Rev 85: 17-28 (1983)