FURFURYL ALCOHOL

98-00-0

2-Furanmethanol

2-Furylmethanol

furan-2-ylmethanol

2-Furancarbinol

Furfural alcohol

2-Furylcarbinol

2-Furanylmethanol

Furfuranol

2-Furfuryl alcohol

Furfurylalcohol

Furfuralcohol

5-Hydroxymethylfuran

2-(Hydroxymethyl)furan

Furyl alcohol

2-Hydroxymethylfuran

Furylcarbinol

alpha-Furylcarbinol

Furan-2-yl-methanol

2-Furfurylalkohol

Furfurylcarb

(2-furyl)methanol

Methanol, (2-furyl)-

2-hydroxymethylfurane

25212-86-6

2-Furane-methanol

Furanmethanol

Furylcarbinol (VAN)

NCI-C56224

2-furanemethanol

FEMA No. 2491

Furan-2-methanol

NSC 8843

(furan-2-yl)methanol

CCRIS 2922

HSDB 711

DTXSID2025347

CHEBI:207496

EINECS 202-626-1

Qo furfuryl alcohol

UNII-D582054MUH

BRN 0106291

Furfurylalcohol-d2

.alpha.-Furylcarbinol

alpha-Furfuryl alcohol

AI3-01171

D582054MUH

NSC-8843

.alpha.-Furfuryl alcohol

DTXCID105347

EC 202-626-1

5-17-03-00338 (Beilstein Handbook Reference)

Furfuryl alcohol, 98%

(2-FURYL)-METHANOL (FURFURYLALCOHOL)

FURFURYL ALCOHOL (IARC)

FURFURYL ALCOHOL [IARC]

2-Furfurylalkohol [Czech]

CAS-98-00-0

FURFURYLALCOHOLRESIN

UN2874

2-Hydroxymethylfuran; 2-Furylmethanol; 2-Furfurylalcohol

furylmethanol

2-Furfurylalcohol

alpha -Furylcarbinol

MFCD00003252

PFFA

(2-furyl)-Methanol

Furfuryl alcohol [UN2874] [Poison]

2-Hydroxymethyl-Furan

alpha -Furfuryl alcohol

Furfuryl alcohol, 8CI

2- FURANCARBINOL

2- FURANYLMETHANOL

2-Furfurylalkohol(CZECH)

Epitope ID:136037

furfuryl alcohol (furfurol)

WLN: T5OJ B1Q

CHEM-REZ 200

2-Furane-methanol (furfurol)

FURFURYL ALCOHOL [MI]

FURFURYL ALCOHOL [FCC]

CHEMBL308187

FURFURYL ALCOHOL [FHFI]

FURFURYL ALCOHOL [HSDB]

CHEBI:53371

FEMA 2491

Furfuryl alcohol, >=97%, FG

NSC8843

2-Furanmethanol (furfuryl alcohol)

2-Furylmethanol (ACD/Name 4.0)

STR01021

Tox21_202102

Tox21_303093

Furfuryl alcohol, analytical standard

AKOS000119178

AM81811

MCULE-4977977402

UN 2874

Furfuryl alcohol [UN2874] [Poison]

Furfuryl alcohol, natural, >=95%, FG

NCGC00249166-01

NCGC00256987-01

NCGC00259651-01

93793-62-5

DB-016149

DB-254877

F0076

NS00003728

EN300-19106

C20441

Q27335

A845784

J-521401

F0001-2310

Z104472794

InChI=1/C5H6O2/c6-4-5-2-1-3-7-5/h1-3,6H,4H

The Henry's Law constant for furfuryl alcohol is estimated as 7.9X10-8 atm-cu m/mole(SRC) derived from its vapor pressure, 0.609 mm Hg(1), and an assigned value for water solubility of 1X10+6 mg/L (miscible)(2). This Henry's Law constant indicates that furfuryl alcohol is expected to be essentially nonvolatile from water surfaces(3). Furfuryl alcohol's estimated Henry's Law constant indicates that volatilization from moist soil surfaces is not expected to occur(SRC). Furfuryl alcohol may 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) McKillip WJ, Sherman E; in Kirk-Othmer Encycl Chem Tech 3rd ed 11: 499-527 (1978) (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 furfuryl alcohol is estimated as 34(SRC), using a log Kow of 0.28(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that furfuryl alcohol is expected to have very high mobility in soil. The pKa of furfuryl alcohol is 9.55(4), indicating that this compound will primarily exist in its neutral form in the environment(5).
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. 13 (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) (4) Serjeant EP, Dempsey B; Ionisation constants of organic acids in aqueous solution. IUPAC Chem Data Ser No.23. NY,NY: Pergamon pp. 989 (1979) (5) Doucette WJ; pp. 141-188 in Handbook of Property Estimation Methods for Chemicals. Boethling RS, Mackay D, eds. Boca Raton, FL: Lewis Publ (2000)

UNDECANOIC ACID

112-37-8

Hendecanoic acid

Undecylic acid

undecanoate

n-Undecanoic acid

n-Undecoic acid

n-Undecylic acid

Undecoic acid

1-Decanecarboxylic acid

FEMA No. 3245

undecanoicacid

Undecanoate [USAN]

Undekansaeure

NSC-7885

CHEBI:32368

MFCD00002730

Undecanoate;Hendecanoic acid

138ON3IIQG

DTXSID8021690

NSC7885

64118-43-0

1-decanecarboxylate

C11:0

NSC 7885

EINECS 203-964-2

UNII-138ON3IIQG

BRN 1759287

AI3-02280

undecansäure

Undecanoic acid, 98%

63400-07-7

bmse000563

SCHEMBL9266

NCIOpen2_009435

4-02-00-01068 (Beilstein Handbook Reference)

WLN: QV10

CH3-[CH2]9-COOH

UNDECANOIC ACID [FHFI]

UNDECANOIC ACID [INCI]

CHEMBL108030

DTXCID001690

GTPL5533

QSPL 035

QSPL 155

QSPL 192

Undecanoic acid, >=97%, FG

HMS3740G13

Tox21_201031

Undecanoic acid, analytical standard

BDBM50511006

LMFA01010011

AKOS000276906

AM85321

CS-W004282

DS-6048

FA 11:0

HY-W004282

MCULE-5110587542

PB44018

NCGC00248901-01

NCGC00258584-01

BP-27912

CAS-112-37-8

SY007756

DB-222294

NS00014192

S9454

U0004

EN300-19485

C17715

P19940

A802562

Q425988

J-002761

75EF58E9-1C6B-4875-8B82-D0B7A10FAEA2

F2191-0248

Z104473988

Phenylacetonitrile

Benzeneacetonitrile

2-Phenylacetonitrile

BENZYL CYANIDE

140-29-4

alpha-Tolunitrile

Benzyl nitrile

alpha-Cyanotoluene

(Cyanomethyl)benzene

Phenyl acetyl nitrile

Benzylnitrile

Acetonitrile, phenyl-

benzylcyanide

Benzylkyanid

Phenyl-acetonitrile

USAF KF-21

Toluene, alpha-cyano-

Acetic acid, phenyl-nitrile

2-phenylethanenitrile

.omega.-Cyanotoluene

CCRIS 4698

NSC 118418

Phenacetonitrile

HSDB 2103

Phenylacetonitrile, liquid

omega-Cyanotoluene

EINECS 205-410-5

.alpha.-Tolunitrile

UNII-23G40PRP93

.alpha.-Cyanotoluene

2-phenyl-acetonitrile

DTXSID2021492

AI3-04975

23G40PRP93

Toluene, .alpha.-cyano-

NSC-118418

BENZYL CYANIDE-13C

DTXCID401492

CHEBI:25979

BENZYL-ALPHA-13C CYANIDE

EC 205-410-5

MFCD00001894

PHENYLACETONITRILE-2,2-D2

BENZYL-D7 CYANIDE, 98 ATOM % D

WLN: NC1R

Benzylkyanid [Czech]

TRIAMTERENE IMPURITY D (EP IMPURITY)

TRIAMTERENE IMPURITY D [EP IMPURITY]

UN2470

enzylcyanide

phenylacetonitile

phenylacteonitrile

Cyanophenylmethane

alpha -cyano-

alpha -tolunitrile

phenyl acetonitrile

BnCN

alpha -cyanotoluene

benzene acetonitrile

benzene-acetonitrile

alpha-Cyano-Toluene

Ethyl2-Fluoroacrylate

alpha-phenylacetonitrile

Benzyl cyanide, 98%

Toluene, alpha -cyano-

Benzeneacetonitrile, 9CI

Benzyl cyanide, >=99%

Phenylacetonitrile, liquid [UN2470] [Poison]

BENZYL CYANIDE [MI]

SCHEMBL37831

BENZYL CYANIDE [HSDB]

laquo Omegaraquo -cyanotoluene

CHEMBL3560735

NSC3407

Benzyl cyanide, analytical standard

NSC-3407

Phenylacetonitrile (Benzyl Cyanide)

Tox21_200217

NSC118418

STL199233

AKOS000118943

MCULE-3500109780

UN 2470

NCGC00090854-01

NCGC00090854-02

NCGC00257771-01

CAS-140-29-4

DB-004016

NS00009919

P0128

Phenylacetonitrile, liquid [UN2470] [Poison]

A807640

Q425620

J-519675

InChI=1/C8H7N/c9-7-6-8-4-2-1-3-5-8/h1-5H,6H

The Henry's Law constant for benzyl cyanide is estimated as 1.4X10-4 atm-cu m/mole(SRC) derived from its vapor pressure, 8.9X10-2 mm Hg(1), and water solubility, 100 mg/L(2). This Henry's Law constant indicates that benzyl cyanide 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 5.7 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 6.4 days(SRC). Benzyl cyanide's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Benzyl cyanide is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(1).
Literature: (1) O'Neil MJ, ed; The Merck Index. 13th ed Whitehouse Station, NJ: Merck and Co., Inc., p.194 (2001) (2) Chemicals Inspection and Testing Institute; Biodegradation and bioaccumulation data of existing chemicals based on the CSCL Japan. Japan Chemical Industry Ecology - Toxicology and Information Center. ISBN 4-89074-101-1 (1992) (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 benzyl cyanide is estimated as 170(SRC), using a log Kow of 1.56(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that benzyl cyanide is expected to have moderate 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. 39 (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)