Caprylsaeure

heptanecarboxylic acid

Kaprylsaeure

capryloate

Octansaeure

Zirconium octanoate

Acidum octanocium

acidum octanoicum

Kyselina kaprylova

octylate

WWZKQHOCKIZLMA-UHFFFAOYSA-N

1-heptanecarboxylate

Acide octanoique

Acido octanoico

n-heptanecarboxylic acid

caprylic acid

octanoic acid

Enantic acid

n-caprylate

n-octanoate

OCA

octoic acid

Octylic acid

1-heptanecarboxylic acid

7-carboxyheptyl

n-octoate

n-octylate

Octic acid

0ctanoic acid

AC1Q2VVU

Caprylic/Capric Acid Blend

Octanoic acid, analytical standard

ACMC-1BTHQ

n-caprylic acid

n-octanoic acid

n-octylic acid

n-Octoic acid

1-octanoic acid

Acid C8

Heptane-1-carboxylic acid

Kyselina kaprylova [Czech]

SCHEMBL3933

AC1L193V

Acide octanoique [French]

Acido octanoico [Spanish]

Acidum octanocium [Latin]

GTPL4585

KSC174S6D

M789

C8H16O2

Caprylic acid (natural)

Hexacid 898

neo-fat 8

Neo-Fat 8S

NSC5024

C-8 acid

C8:0

Caprylic Acid 657

CTK0H4961

Emery 657

HMDB00482

HSDB 821

Kortacid 0899

O0027

OBL58JN025

OCTANOIC ACID (CAPRYLIC ACID)

Octanoic acid (mixed isomers)

Octanoic acid (USAN)

QSPL 011

QSPL 184

WLN: QV7

Caprylic acid (NF)

CHEMBL324846

DB04519

LS-691

NE10316

Octanoic acid, >=98%

Octanoic acid, >=99%

Prifac 2901

bmse000502

C06423

Caprylic acid, European Pharmacopoeia (EP) Reference Standard

CCRIS 4689

D05220

HMS2270A23

UNII-OBL58JN025

AN-1411

DTXSID3021645

LP078155

LP097945

NSC 5024

NSC-5024

Octanoic acid (USAN/INN)

Octanoic acid [USAN:INN]

SBB060020

STL282742

UNII-DI775RT244 component WWZKQHOCKIZLMA-UHFFFAOYSA-N

Caprylic acid, United States Pharmacopeia (USP) Reference Standard

CHEBI:28837

DSSTox_CID_1645

Lunac 8-95

Lunac 8-98

Octanoic acid, certified reference material, TraceCERT(R)

ZINC1530416

ANW-18188

DSSTox_GSID_21645

DSSTox_RID_76259

Fatty acids, C6-1O

LMFA01010008

MFCD00004429

AI3-04162

NCIOpen2_002902

NCIOpen2_009358

Octanoic acid, >=96.0%

RTR-003747

ST51046283

TR-003747

AKOS000118802

I04-1204

J-005040

Octanoic acid, >=98%, FG

BRN 1747180

Fatty acids, C6-10

FEMA No. 2799

FT-0660765

MLS002415762

SMR001252279

C8:0 (Lipid numbers)

CH3-[CH2]6-COOH

Z955123584

Tox21_111045

Tox21_201279

Tox21_300345

124-07-2

Octanoic acid, natural, >=98%, FG

Octanoic acid, zirconium salt (1:?)

Caprylic Acid (Octanoic Acid), pharmaceutical secondary standard; traceable to USP and PhEur

MCULE-5193957469

NCGC00090957-01

NCGC00090957-02

NCGC00090957-03

NCGC00090957-04

NCGC00254446-01

NCGC00258831-01

Octanoic acid, for synthesis, 99.5%

CAS-124-07-2

EINECS 204-677-5

EINECS 242-197-8

EINECS 273-085-7

68937-74-6

597-EP2269988A2

597-EP2270008A1

597-EP2275413A1

597-EP2287156A1

597-EP2292617A1

597-EP2298780A1

597-EP2301940A1

597-EP2305689A1

597-EP2311807A1

597-EP2311824A1

597-EP2374787A1

SR-01000865607

MolPort-001-792-057

124-07-2 (Parent)

1984-06-1 (hydrochloride salt)

6535-19-9 (unspecified manganese salt)

764-71-6 (potassium salt)

146488-EP2280007A1

146488-EP2292597A1

SR-01000865607-2

18312-04-4 (unspecified zirconium salt)

557-09-5 (zinc salt)

5972-76-9 (ammonium salt)

6028-57-5 (aluminum salt)

20195-23-7 (unspecified chromium salt)

2191-10-8 (cadmium salt)

4696-54-2 (barium salt)

6107-56-8 (calcium salt)

6535-20-2 (unspecified iron salt)

6700-85-2 (cobalt salt)

20543-04-8 (unspecified copper salt)

7435-02-1 (unspecified Ce salt)

15696-43-2 (unspecified lead salt)

16577-52-9 (lithium salt)

4-02-00-00982 (Beilstein Handbook Reference)

5206-47-3 (zirconium(+4) salt)

6427-90-3 (chromium(+2) salt)

3890-89-9 (copper(+2) salt)

4995-91-9 (nickel(+2) salt)

3130-28-7 (iron(+3) salt)

7319-86-0 (lead(+2) salt)

1912-83-0 (tin(+2) salt)

60903-69-7 (La(+3) salt)

67816-08-4 (Ir(+3) salt)

68957-64-2 (Ru(+3) salt)

43FDA9D7-2300-41E7-A373-A34F25B81553

A pKa of 4.89(1) indicates octanoic 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). Octanoic acid is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 3.71X10-3 mm Hg(3).
Literature: (1) Dean JA; Handbook of Organic Chemistry, NY, NY: McGraw-Hill, Inc p. 8-45 (1987) (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., Washington, DC: Taylor & Francis, Vol 4 (1995)

The Koc of undissociated octanoic acid is estimated as 1,100 for the free acid(SRC), using a log Kow of 3.05(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that undissociated octanoic acid is expected to have low mobility in soil. The pKa of octanoic acid is 4.89(4), indicating that this compound will exist almost entirely in the anion form in the environment and anions generally do not adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(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. 49 (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) Dean JA; Handbook of Organic Chemistry, NY, NY: McGraw-Hill, Inc p. 8-45 (1987) (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)

Benzylcarboxaldehyde

Benzenacetaldehyde

Benzeneacetaldehyde

phenylacetaldehyde

Phenylacetoaldehyde

Benzacetaldehyde

Phenacetaldehyde

alpha-Phenylacetaldehyde

benzeneethanal

Oxophenylethane

Phenylacetic aldehyde

Phenylethanal

a-Phenylacetaldehyde

Hyacinthin

phenyl acetaldehyde

phenyl acetoaldehyde

phenyl-Acetaldehyde

alpha-Tolualdehyde

alpha-Tolyaldehyde

DTUQWGWMVIHBKE-UHFFFAOYSA-N

PHENYLACETALDEHYDE, MONOMER

2-phenylacetaldehyde

a-Tolualdehyde

a-Tolyaldehyde

alpha-Toluic aldehyde

2-Phenylethanal

Phenylacetaldehyde (natural)

2-phenyl-acetaldehyde

a-toluic aldehyde

AC1Q6QIR

AC1Q6QJB

HY1

Phenylacetaldehyde, >=90%

Acetaldehyde, phenyl-

U8J5PLW9MR

.alpha.-Tolualdehyde

AC1L1AI5

UNII-U8J5PLW9MR

KSC174S9R

.alpha.-Toluic aldehyde

ACMC-209uaw

PubChem19675

SCHEMBL18972

CTK0H4998

HMDB06236

P0119

1-Oxo-2-phenylethane

DB02178

Phenylacetaldehyde solution, technical, ~50% in diethyl phthalate

RP19376

bmse000427

C00601

ZINC895323

AK159198

BC250050

CHEMBL1233464

DTXSID3021483

Jsp001532

LS-3037

NSC406309

OR025047

OR209763

OR244402

SBB061710

ZB015022

A804962

CHEBI:16424

DSSTox_CID_1483

AJ-24176

AN-22889

ANW-43542

DSSTox_GSID_21483

SC-19014

TRA0034790

DSSTox_RID_76177

MFCD00006993

ZINC00895323

AI3-02175

DB-041686

NCIOpen2_003602

NSC 406309

NSC-406309

Phenylacetaldehyde, >=95%, FCC, FG

RTR-003630

ST24041010

ST51047695

TR-003630

Acetaldehyde, phenyl- (8CI)

AKOS000119316

I01-0480

Q-201558

FEMA No. 2974

Tox21_201582

Tox21_302945

122-78-1

F2190-0653

ETHYL, 1-OXO-2-PHENYL-

MCULE-3725701027

NCGC00249076-01

NCGC00256522-01

NCGC00259131-01

CAS-122-78-1

EINECS 204-574-5

MolPort-001-780-108

11967-EP2272517A1

11967-EP2287159A1

11967-EP2301534A1

11967-EP2305671A1

11967-EP2308848A1

11967-EP2311451A1

11967-EP2311840A1

11967-EP2316450A1

11967-EP2374783A1

11967-EP2377841A1

Phenylacetaldehyde solution, natural, 10 wt. % in ethanol, FG

D60A2590-0A65-4BA8-A05B-D8423408535C

InChI=1/C8H8O/c9-7-6-8-4-2-1-3-5-8/h1-5,7H,6H

Alcanfor

Alphanon

Camphora

DSSYKIVIOFKYAU-UHFFFAOYSA-N

Matricaria camphor

camphor

Formosa

Formosa camphor

Japanese camphor

Kampfer

Japan camphor

Laurel camphor

Camphor oil

Camphor USP

dextro,laevo-camphor

Gum camphor

Camphor, synthetic

DL-Camphor

l-Camphor

2-Camphanone

2-Camphonone

AC1L1DWH

Huile de camphre

Root bark spirit

Spirit of camphor

2-Bornanone

2-Kamfanon

Root bark oil

AC1Q2CF0

camphor (natural)

Camphor Powder - Synthetic

d-2-Bornanone

d-2-Camphanone

Bornan-2-one

GTPL2422

HSDB 37

Kampfer [German]

KSC378C7P

Q964

Camphor (USP)

CHEMBL15768

SCHEMBL16068

UN2717

C1251

camphor, (synthetic)

Camphor, D-

CTK2H8177

HMS502E06

1,7,7-Trimethylnorcamphor

DL-Bornan-2-one

JFD03998

LS-126

(1R)-Camphor

C00809

C18369

D00098

HMS2268A06

Huile de camphre [French]

Sarna (Salt/Mix)

AC-5284

BBL012963

BT000174

DTXSID5030955

Heet (Salt/Mix)

LS-1691

OR001346

OR116929

OR327727

STK803534

UN 2717

(-)-Alcanfor

2-Kamfanon [Czech]

A838646

ACMC-209k77

CHEBI:36773

D(+)-Camphor

(-)-Camphor

(+)-Camphor

AC-15523

AN-11174

AN-17868

AN-23465

AN-23893

ANW-30449

Bornane, 2-oxo-

DSSTox_GSID_30955

KB-00097

KB-50285

LS-48718

TRA0077646

BB_NC-0198

CAMPHOR POWDER D.A.B.8

Caswell No. 155

DSSTox_CID_10955

DSSTox_RID_78860

MFCD00064149

NINDS_000724

AI3-01698

AI3-18783

Camphor, (1R)-Isomer

DB-070734

dl-Camphor (JP17)

KB-270826

RTR-037701

TR-037701

2-Keto-1,7,7-trimethylnorcamphane

AKOS000118728

AKOS022060577

D-(+)-Camphor

DivK1c_000724

EPA Pesticide Chemical Code 015602

I06-1217

KBio1_000724

l-(-)-Camphor

Q-200784

W-109539

W-110530

(+-)-Camphor

BRN 1907611

BRN 3196099

FEMA No. 2230

FT-0607017

IDI1_000724

MLS001055495

SMR000386909

(+)-2-Bornanone

1,7,7-trimethylnorbornan-2-one

76-22-2

I14-16513

LMPR0102120001

Z940713494

Tox21_200237

464-48-2

F0001-0763

(+/-)-Camphor

Camphor, (+)-

CAS-76-22-2

Norcamphor, 1,7,7-trimethyl-

Camphor, (+-)-Isomer

MCULE-2476865084

NCGC00090681-05

NCGC00090730-01

NCGC00090730-02

NCGC00257791-01

EINECS 200-945-0

EINECS 207-355-2

EINECS 244-350-4

21368-68-3

CAMPHOR, (+-)-

(1R)-(+) Camphor

(1R)-(+)-amphor

MolPort-002-506-944

Camphor, synthetic [UN2717] [Flammable solid]

(.+/-.)-Camphor

Camphor, (+/-)-

(1R, 4R)-(+) Camphor

(1R,4R)-1,7,7-trimethylnorbornan-2-one

Camphor, (.+/-.)-

1,7,7-Trimethylbicyclo(2.2.1)-2-heptanone

1,7,7-Trimethylbicyclo(2.2.1)heptan-2-one

1,7,7-Trimethylbicyclo[2.2.1]-2-heptanone

1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one

4,7,7-trimethyl-3-bicyclo[2.2.1]heptanone

4,7,7-trimethylbicyclo[2.2.1]heptan-3-one

Camphor, (1R,4R)-(+)-

1,7,7-Trimethyl-bicyclo(2,2,1)Heptan-2-one

1,7,7-Trimethyl-bicyclo[2.2.1]heptan-2-one

1,7,7-trimethyl-bicyclo[2.2.1]heptan-6-one

(+/-)-Camphor, 96% 100g

Bicyclo(2.2.1)heptane-2-one, 1,7,7-trimethyl-

Bicyclo[2.2.1]heptane-2-one, 1,7,7-trimethyl-

Bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl-

Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-

(+/-)-1,7,7-trimethyl-bicyclo[2,2,1]heptane-2-one

Bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl-, (1theta)-

Bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl-, (1R)-

Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1R)-

Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1S)-

Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1S,4S)-

Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (+/-)-

CAMPHOR (SEE ALSO DL-CAMPHOR (21368-68-3) AND D-CAMPHOR (464-49-3))

Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (.+/-.)-

DL-CAMPHOR (SEE ALSO D-CAMPHOR (464-49-3) AND DL-CAMPHOR (21368-68-3))

The Henry's Law constant for camphor is estimated as 8.3X10-5 atm-cu m/mole(SRC) derived from its vapor pressure, 0.65 mm Hg(1), and water solubility, 1.570X10+3 mg/L(2). This Henry's Law constant indicates that camphor 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 17 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 9 days(SRC). Camphor's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Camphor is expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(1).
Literature: (1) Jones AH; J Chem Eng Data 5: 196-200 (1960) (2) Yalkowky SH et al; Handbook of Aqueous Solubility Data. 2nd ed., Boca Raton, FL: CRC Press, p. 721 (2010) (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 camphor can be estimated to be 117(SRC). According to a classification scheme(2), this estimated Koc value suggests that camphor is expected to have high mobility in soil.
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.11. Nov, 2012. Available from, as of May 21, 2014: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Swann RL et al; Res Rev 85: 17-28 (1983)

Dodecylcarboxylate

Laurinsaeure

laurostearate

dodecylate

Laurostearic acid

POULHZVOKOAJMA-UHFFFAOYSA-N

1-undecanecarboxylate

DODECANOIC ACID

Duodecyclic acid

Duodecylic acid

vulvate

Acide Laurique

dodecanic acid

Dodecoic acid

Dodecylic acid

n-Dodecanoate

1-Undecanecarboxylic acid

ABL

DAO

Dodecanoic Acid Anion

LAP

LAU

lauric acid

Vulvic acid

Dodecanoic acid, analytical standard

Lauric Acid Kosher

3uil

Dodecanoic acid, typically

n-Dodecanoic acid

ACMC-1BTHL

Coconut oil fatty acids

dilauric acid;

Undecane-1-carboxylic acid

AC1L1GY2

AC1Q5W8C

Dodecanoic acid(Lauric acid)

Lauric acid, pure

SCHEMBL5895

Dodecanoic (Lauric) acid

GTPL5534

KSC176I2N

Ninol AA62 Extra

C12 fatty acid

NSC5026

OA(1)ethEa

CCRIS 669

CTK0H6426

Dodecanoic acid (lauric acid)

Emery 650

Emery 651

HMDB00638

Hystrene 9512

Kortacid 1299

L0011

Lauric acid (natural)

Philacid 1200

Wecoline 1295

CHEMBL108766

Dodecanoic acid, 98%

Dodecanoic acid, 99%

Lauric Acid 652

LS-845

Lunac L 70

Lunac L 98

Neo-fat 12

OR55016

Prifac 2920

Prifrac 2920

1160N9NU9U

Aliphat No. 4

bmse000509

C02679

C12:0

D10714

HMS2268C14

HMS3649N06

HSDB 6814

Hydrofol acid 1255

Hydrofol acid 1295

Lauric acid (NF)

Nissan NAA 122

WLN: QV11

DTXSID5021590

Lauric acid, European Pharmacopoeia (EP) Reference Standard

LP003931

NSC-5026

SBB060023

ST023796

STL281860

Univol U 314

Univol U-314

C-1297

CHEBI:30805

DODECANOIC ACID (LAURIC ACID)

DSSTox_CID_1590

UNII-1160N9NU9U

ZINC1529498

AC-16451

AN-23253

ANW-20737

DSSTox_GSID_21590

EBD2203547

Lauric acid, United States Pharmacopeia (USP) Reference Standard

TRA0004834

Dodecanoic acid, >=99.5%

DSSTox_RID_76223

Lauric Acid, pharmaceutical secondary standard; traceable to USP, PhEur

LMFA01010012

MFCD00002736

AI3-00112

NCIOpen2_009480

RTR-035707

TR-035707

AKOS000277433

I04-1205

J-007739

BRN 1099477

Dodecanoic acid, >10% in a non hazardous diluent

Duodecylic acidC12:0 (Lipid numbers)

FEMA No. 2614

FT-0625572

MLS002177807

MLS002415737

Neo-fat 12-43

SMR001253907

Dodecanoic acid, >=99% (GC/titration)

Z966690584

Tox21_202149

Tox21_303010

143-07-7

CH3-[CH2]10-COOH

7632-48-6

8000-62-2

9054-63-1

Dodecanoic acid, 98% 500g

MCULE-2795129925

NCGC00090919-01

NCGC00090919-02

NCGC00090919-03

NCGC00256486-01

NCGC00259698-01

CAS-143-07-7

Edenor C 1298-100

EINECS 205-582-1

Lauric acid, >=98%, FCC, FG

203714-07-2

LAURIC ACID, 99.5% (GLC)

MolPort-000-881-524

629-25-4 (hydrochloride salt)

Lauric acid, natural, >=98%, FCC, FG

Dodecanoic acid, purum, >=96.0% (GC)

2437-23-2 (ammonium salt)

4040-48-6 (magnesium salt)

4696-56-4 (calcium salt)

10124-65-9 (potassium salt)

15337-60-7 (unspecified barium.cadmium salt)

14622-13-0 (lithium salt)

4-02-00-01082 (Beilstein Handbook Reference)

[2-((1-OXODODECANOXY-(2-HYDROXY-3-PROPANYL))-PHOSPHONATE-OXY)-ETHYL]-TRIMETHYLAMMONIUM

76C2A2EB-E8BA-40A6-8032-40A98625ED7B

InChI=1/C12H24O2/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h2-11H2,1H3,(H,13,14

A pKa of 5.3(1) indicates dodecanoic 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). Dodecanoic acid is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 1.6X10-5 mm Hg(3).
Literature: (1) Serjeant EP, Dempsey B; IUPAC Chemical Data Series No 23 NY, NY: Pergamon Press (1979) (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) Yaws CL; Handbook of Vapor Pressure. Vol 3: C8-C28 Compounds. Houston, TX: Gulf Pub Co (1994)

The Koc of undissociated dodecanoic acid is estimated as 7,600 for the free acid(SRC), using a log Kow of 4.60(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that undissociated dodecanoic acid is expected to be immobile in soil. The pKa of dodecanoic acid is 5.3(4) , 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(5).
Literature: (1) Sangster J; LOGKOW Databank. Sangster Res Lab Montreal Quebec, Canada (1994) (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; IUPAC Chemical Data Series No 23 NY, NY: Pergamon Press (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)

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)

methylpentylketone

Butylacetone

2-heptanone_GurudeebanSatyavani

CATSNJVOTSVZJV-UHFFFAOYSA-N

Heptanone

Butyl acetone

HTX

Methyl pentyl ketone

Pentyl methyl ketone

1-Methylhexanal

Amyl methyl ketone

Amyl-methyl-cetone

Methyl amyl ketone

Methyl-amyl-cetone

Methyl-n-amylketone

2-Ketoheptane

2-Oxoheptane

2-heptanal

2-HEPTANONE

6-oxoheptyl

ACMC-1CMSN

heptanone-2

Ketone, methyl pentyl

Methyl n-pentyl ketone

n-Pentyl methyl ketone

AC1L1Q5I

Methyl n-amyl ketone

n-Amyl methyl ketone

2-Heptanone, analytical standard

Heptan-2-one

KSC175M3T

Methyl n-Amyl Ketone Reagent Grade

7785AF

CHEMBL18893

Ketone C-7

NSC7313

SCHEMBL29364

UN1110

CTK0H5639

HMDB03671

Nat. 2-Heptanone

Amyl-methyl-cetone [French]

Methyl Amyl Ketone (Fragrance Grade)

Methyl-amyl-cetone [French]

n-C5H11COCH3

RL00436

2-Heptanone (natural)

2-Heptanone(Methyl Amyl Ketone)

89VVP1B008

C08380

CCRIS 8809

CHEBI:5672

HSDB 1122

WLN: 5V1

2-OXOHEPTAN-3-YL

BBL011381

DTXSID5021916

FEMA Number 2544

Jsp000804

LP084116

LP100158

LP100159

LS-2784

NSC 7313

NSC-7313

OR034045

SBB061125

SCHEMBL1122991

STL146482

UN 1110

A802193

DSSTox_CID_1916

UNII-89VVP1B008

ZINC1531087

2-Heptanone, 98%

2-Heptanone, 99%

AN-22605

ANW-16152

CJ-05231

CJ-24088

DSSTox_GSID_21916

KB-68767

SC-19092

ACN-S002378

BB_SC-6722

BDBM50028842

DSSTox_RID_76400

LMFA12000004

MFCD00009513

ZINC01531087

AI3-01230

RTR-002152

ST51047182

TR-002152

AKOS000120708

I14-5855

J-509557

BRN 1699063

FEMA No. 2544

FT-0612484

TRA-0205300

Tox21_202164

Tox21_302935

110-43-0

MCULE-6017828463

NCGC00249180-01

NCGC00256611-01

NCGC00259713-01

CAS-110-43-0

EINECS 203-767-1

29299-43-2

2-Heptanone, natural, 98%, FG

2-Heptanone, >=98%, FCC, FG

2-Heptanone, 99% 100ml

MolPort-001-759-309

26073-EP2281810A1

26073-EP2289965A1

26073-EP2314558A1

n-Amyl methyl ketone [UN1110] [Flammable liquid]

n-Amyl methyl ketone [UN1110] [Flammable liquid]

4-01-00-03318 (Beilstein Handbook Reference)

InChI=1/C7H14O/c1-3-4-5-6-7(2)8/h3-6H2,1-2H

An experimental Henry's Law constant of 1.69X10-4 atm cu m/mole at 25 deg C(1) indicates that 2-heptanone 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 4.8 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)(2) is estimated as 6 days(SRC). 2-Heptanone's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). 2-Heptanone is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 3.86 mm Hg(3).
Literature: (1) Shiu WY, Mackay, D; J Chem Eng Data 42: 27-30 (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) Riddick JA et al; Organic Solvents 4th ed. NY: Wiley Interscience (1986)

The Koc of 2-heptonone is estimated as 280(SRC), using a log Kow of 1.98(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that 2-heptanone 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. 35 (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)

BKIMMITUMNQMOS-UHFFFAOYSA-N

NONANE

OyEEIe

nonan

Nonyl hydride

nonyl group

Nonane, analytical standard

AC1L1QCW

AC1Q2VWN

DD9

n-Nonane

n-nonyl radical

Fluorochemical surfactant, Zwitterionic / non-ionic

Heptane, ethyl-

KSC181E3H

Shellsol 140

CTK0I1233

HSDB 107

N0286

S0281

T9W3VH6G10

ACMC-2099ay

CHEMBL335900

Fluorochemical surfactant, anionic / non-ionic

LS-541

n-C9H20

Nonane, 99%

NSC72430

CCRIS 6081

LTBB002319

UNII-T9W3VH6G10

DTXSID9025796

Jsp000889

LP004031

LP067689

Nonane, anhydrous, >=99%

UN 1920

A802420

CHEBI:32892

DSSTox_CID_5796

ZINC1698517

ANW-16328

DSSTox_GSID_25796

NONANE MFC9 H20

NSC 72430

NSC-72430

SC-96410

TRA0006056

DSSTox_RID_77926

LMFA11000579

MFCD00009574

MFCD02099450

DB-041010

RTR-002319

TR-002319

AKOS015904046

W-108667

FT-0626750

FT-0631631

I14-17869

Nonane, ReagentPlus(R), 99%

Tox21_201479

Tox21_303148

111-84-2

CH3-[CH2]7-CH3

MCULE-1865327912

NCGC00091787-01

NCGC00091787-02

NCGC00257029-01

NCGC00259030-01

CAS-111-84-2

EINECS 203-913-4

32757-65-6

61193-19-9

66039-00-7

n-Nonane, 99% 100ml

MolPort-003-929-477

15417-EP2275407A1

15417-EP2275469A1

15417-EP2287940A1

15417-EP2289965A1

15417-EP2298828A1

15417-EP2301983A1

15417-EP2305683A1

15417-EP2308926A1

15417-EP2309564A1

15417-EP2311839A1

15417-EP2314589A1

15417-EP2316837A1

72705-EP2269986A1

72705-EP2277871A1

72705-EP2289509A2

72705-EP2292576A2

72705-EP2308492A1

72705-EP2371811A2

72705-EP2380568A1

178017-EP2277868A1

178017-EP2277869A1

178017-EP2277870A1

C8F3CAB9-DAF5-4085-84EB-07C0AB04D3A1

InChI=1/C9H20/c1-3-5-7-9-8-6-4-2/h3-9H2,1-2H

The Henry's Law constant for n-nonane is estimated as 3.4 atm-cu m/mole(SRC) derived from its vapor pressure, 4.45 mm Hg(1), and water solubility, 22 mg/L)(2). This Henry's Law constant indicates that n-nonane 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 3.3 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 4.5 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 155 days if adsorption is considered(4). n-Nonane's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of n-nonane from dry soil surfaces may exist(SRC) based upon the 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) Riddick JA et al; Techniques of Chemistry. 4th ed. Volume II. Organic Solvents. New York, NY: John Wiley and Sons (1985) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (4) US EPA; EXAMS II Computer Simulation (1987)

The Koc of n-nonane is estimated as 8.0X10+4(SRC), using a log Kow of 5.65(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that n-nonane is expected to be immobile in soil. Freundlich absorption coefficients of log 4.50 and log 4.01 were measured in Oberlausitz lignite (11.1% moisture content; 53.5 wt% carbon content; 0.6 wt % nitrogen content) and Pahokee peat soil (10.2% moisture content; 46.1 wt% carbon content; 3.3 wt % nitrogen content), respectively(4).
Literature: (1) Sangster J; LOGKOW Database. A databank of evaluated octanol-water partition coefficients (Log P). Available from, as of Oct 30, 2013: http://logkow.cisti.nrc.ca/logkow/search.html (2) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Nov, 2012. Available from, as of Oct 30, 2013: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (3) Swann RL et al; Res Rev 85: 17-28 (1983) (4) Endo S et al; Environ Sci Technol 42): 5897-5903 (2008)

Pelargonsaeure

NoEthaCoEa

Nonansaeure

FBUKVWPVBMHYJY-UHFFFAOYSA-N

Nonanoate

Pelargon

pergonate

nonans

Pelargonic acid

1-octanecarboxylate

n-Pelargonate

NONANOIC ACID

Pelargic acid

pergonic acid

Caprylic-Capric Acid

IioA inverted question markuEa

KNA

Nonoic acid

Nonylic acid

1-Octanecarboxylic acid

8-carboxyoctyl

n-Nonoate

n-Nonylate

Nonanoic Acid Anion

1-Octanecarboxyic acid

n-pelargonic acid

Nonanoic acid, analytical standard

1-nonanoate

n-Nonanoic acid

n-Nonylic acid

3sz1

n-Nonoic acid

1-nonanoic acid

AC1L1QE7

AC1Q2VX7

AC1Q5W5X

Acid C9

octan-1 carboxylic acid

Pelargon [Russian]

Cirrasol 185A

Hexacid C-9

KSC175A3N

C9H18O2

SCHEMBL21966

C9:0

CTK0H5036

HMDB00847

N0288

P0952

QSPL 030

WLN: QV8

ACMC-2099ce

Caprylic-Capric Acid 658

CHEMBL108436

Nonanoic acid, >=97%

NSC62787

Pelargonic Acid 1202

97SEH7577T

bmse000499

C01601

Emery 1202

Emery 1203

Emery's L-114

Emfac 1202

HMS2269L08

HSDB 5554

Nonanoic acid, 96%

BBL027459

DTXSID3021641

Jsp000917

LP067835

LP097946

LS-2986

SBB058693

STL372710

A802476

CHEBI:29019

DSSTox_CID_1641

UNII-97SEH7577T

ZINC1529234

AN-43106

ANW-16380

DSSTox_GSID_21641

KB-58725

NSC 62787

NSC-62787

BB_SC-7262

DSSTox_RID_76255

Fatty acids, C8-1O

LMFA01010009

MFCD00004433

AI3-04164

CCG-231471

NCIOpen2_000142

NCIOpen2_000179

NCIOpen2_001763

NCIOpen2_002882

NCIOpen2_003483

RTR-002359

ST51037369

TR-002359

AKOS000118981

BB_SC-07262

EPA Pesticide Chemical Code 217500

Nonanoic acid, >=96%, FG

Q-201488

S04-0163

BRN 1752351

Fatty acids, C6-12

Fatty acids, C8-10

FEMA No. 2784

FT-0660055

FT-0695195

MLS001066339

SMR000112203

CH3-[CH2]7-COOH

Tox21_202426

Tox21_300022

112-05-0

NONANOIC ACID MFC9 H18 O2

Z1258948135

Nonanoic acid, natural, 98%, FG

Emery 1202 (Salt/Mix)

MCULE-4736597375

NCGC00164328-01

NCGC00164328-02

NCGC00164328-03

NCGC00253958-01

NCGC00259975-01

CAS-112-05-0

EINECS 203-931-2

EINECS 273-086-2

58253-02-4

68937-75-7

MolPort-000-881-522

83478-EP2305655A2

14047-60-0 (hydrochloride salt)

5112-16-3 (cadmium salt)

23282-34-0 (potassium salt)

7640-78-0 (zinc salt)

29813-38-5 (calcium salt)

4-02-00-01018 (Beilstein Handbook Reference)

F57B4D17-8824-403B-AE1B-FA425608BB39

InChI=1/C9H18O2/c1-2-3-4-5-6-7-8-9(10)11/h2-8H2,1H3,(H,10,11

A pKa of 4.95(1) indicates nonanoic 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). Nonanoic acid is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 1.65X10-3 mm Hg(3).
Literature: (1) Dean JA; Handbook of Organic Chemistry, NY, NY: McGraw-Hill, Inc p. 8-45 (1987) (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., Washington, DC: Taylor & Francis, Vol 4 (1995)

The Koc of undissociated nonanoic acid is estimated as 1,700 for the free acid(SRC), using a log Kow of 3.42(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that undissociated nonanoic acid is expected to have low mobility in soil. The pKa of nonanoic acid is 4.95(4), 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(5).
Literature: (1) Sangster J; LOGKOW Databank, Sangster Res Lab, Montreal Quebec, Canada (1994) (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) Dean JA; Handbook of Organic Chemistry, NY, NY: McGraw-Hill, Inc p. 8-45 (1987) (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)

Methylnonylketone

UNDECANONE

KYWIYKKSMDLRDC-UHFFFAOYSA-N

Rue ketone

Nonyl methyl ketone

Methyl nonyl ketone

2-Hendecanone

2-Oxoundecane

2-Undecanone

AC1L1QEM

2-undecanon

Methyl Nonyl Ketone FCC

YV5DSO8CY9

METHYL N-NONYL KETONE

Ketone, methyl nonyl

AC1Q5H8X

UNII-YV5DSO8CY9

Undecan-2-one

KSC176M2T

L352

MGK Dog and Cat Repellent

ACMC-1C77Q

Mgk dog & cat repellent

NSC4028

U0006

CTK0H6629

DB08688

SCHEMBL117635

SCHEMBL249443

Undecanone-(2)

C01875

HSDB 7431

WLN: 9V1

2-Undecanone (natural)

SBB060389

AN-1415

NSC-4028

NSC 4028

STL146552

LS-3143

LP003930

Jsp000923

BBL011441

CHEMBL1236582

DTXSID2021943

ZINC1529305

CHEBI:17700

DSSTox_CID_1943

A802493

DSSTox_GSID_21943

ANW-16393

Caswell No. 573O

2-Undecanone, 99%

LMFA12000002

BB_SC-6944

MFCD00009583

DSSTox_RID_76418

AI3-03081

TR-002375

ST51046579

RTR-002375

Q-201393

EPA Pesticide Chemical Code 044102

Methyl nonyl ketone (MNK) Nonyl methyl ketone Methyldecananone 2-Hendecanone Undecanone IBI-246

BB_SC-06944

AKOS005720838

FEMA No. 3093

FT-0613466

BRN 1749573

I14-10598

2-Undecanone, natural, FCC, FG

Tox21_301385

112-12-9

MCULE-6858373499

NCGC00255160-01

NCGC00164003-01

CAS-112-12-9

EINECS 203-937-5

53452-70-3

2-Undecanone, >=98%, FCC, FG

MolPort-003-933-723

The Henry's Law constant for 2-undecanone is 6.36X10-5 atm-cu m/mole(1). This Henry's Law constant indicates that 2-undecanone 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 13 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 11 days(SRC). 2-Undecanone's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). 2-Undecanone is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 4.1X10-2 mm Hg(3).
Literature: (1) Buttery RG et al: J Agric Food Chem 17:385-9 (1960) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Perry RH, Green D; Perry's Chemical Handbook. Physical and Chemical data. NY,NY: McGraw-Hill 6th ed (1984)

Insoluble in water. Soluble in ethanol, ether, acetone, benzene, carbon tetrachloride, chloroform.
Literature: Lide, D.R., G.W.A. Milne (eds.). Handbook of Data on Organic Compounds. Volume I. 3rd ed. CRC Press, Inc. Boca Raton ,FL. 1994., p. V5: 5176
Literature: #In water, 20 mg/L at 25 deg C (est)
Literature: US EPA; Estimation Program Interface (EPI) Suite. Ver.3.12. Nov 30, 2004. Available from, as of Mar 3, 2006: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm

Using a structure estimation method based on molecular connectivity indices(1), the Koc of 2-undecanone can be estimated to be 278(SRC). According to a classification scheme(2), this estimated Koc value suggests that 2-undecanone 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: 17-28 (1983)