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

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)

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)

Caprinaldehyde

Decanaldehyde

Capraldehyde

DECALDEHYDE

Caprinic aldehyde

KSMVZQYAVGTKIV-UHFFFAOYSA-N

KSMVZQYAVGTKIV-UHFFFAOYSA-

n-DECYLALDEHYDE

Capric aldehyde

Decylic aldehyde

Decanal

n-Decaldehyde

Decyl aldehyde

n-Decanal

Decanal, analytical standard

n-Decyl aldehyde

AC1Q2VYO

AC1L1QFM

1-Decanal

Aldehyde C10

1-Decyl aldehyde

SCHEMBL2540

Decanal (natural)

KSC176G3J

U211

NSC6087

ACMC-1C59Q

C-10 aldehyde

D0032

CTK0H6334

Aldehyde C-10

HSDB 288

31Z90Q7KQJ

WLN: VH9

HMDB11623

NE10468

N-decanal (capric aldehyde)

1-Decanal(mixed isomers)

C12307

UNII-31Z90Q7KQJ

LS-2367

CHEMBL2228377

LP001404

NSC 6087

NSC-6087

DTXSID4021553

SBB058676

Jsp000949

ZINC1693270

A802551

CHEBI:31457

DSSTox_CID_1553

ANW-16447

AN-22691

Natural Decanal(C-10)

KB-49635

EBD2219840

SC-22770

DSSTox_GSID_21553

AK-44487

TRA0073044

MFCD00007031

LMFA06000052

DSSTox_RID_76207

ST24030299

AI3-04860

DB-041074

ST51037233

RTR-002413

TR-002413

AKOS000120018

S14-1463

J-002749

FEMA No. 2362

BRN 1362530

FT-0631643

I14-13645

Decanal, natural, >=97%, FG

Tox21_302656

EN300-20146

112-81-2

112-31-2

decanal (ACD/Name 4.0)

Decanal, >=95%, FCC, FG

NCGC00256769-01

CAS-112-31-2

Decanal, >=98% (GC), liquid

EINECS 203-957-4

MolPort-001-769-696

InChI=1/C10H20O/c1-2-3-4-5-6-7-8-9-10-11/h10H,2-9H2,1H3

The Henry's Law constant for decaldehyde is 1.8x10-3 atm-cu m/mole(1). This Henry's Law constant indicates that decaldehyde 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 2 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 5 days(SRC). Decaldehyde's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Decaldehyde is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.103 mm Hg(3).
Literature: (1) Zhou X, Mopper K; Environ Sci Technol 24: 1482-5 (1990) (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)

In water 0.00156 mg/L at 25 deg C
Literature: Yalkowsky, S.H., He, Yan, Jain, P. Handbook of Aqueous Solubility Data Second Edition. CRC Press, Boca Raton, FL 2010, p. 739
Literature: #Soluble in ethanol, ether, acetone; slightly soluble in carbon tetrachloride
Literature: Haynes, W.M. (ed.). CRC Handbook of Chemistry and Physics. 95th Edition. CRC Press LLC, Boca Raton: FL 2014-2015, p. 3-142
Literature: #Soluble in 80% alcohol, fixed oils, volatile oils, mineral oil; insoluble in glycerol
Literature: Lewis, R.J. Sr.; Hawley's Condensed Chemical Dictionary 15th Edition. John Wiley & Sons, Inc. New York, NY 2007., p. 371

Using a structure estimation method based on molecular connectivity indices(1), the Koc of decaldehyde can be estimated to be 70(SRC). According to a classification scheme(2), this estimated Koc value suggests that decaldehyde 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 20, 2015: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Swann RL et al; Res Rev 85: 17-28 (1983)

Pentanecarboxylic acid

pentylformate

capronate

FUZZWVXGSFPDMH-UHFFFAOYSA-N

hexylate

Kyselina kapronova

Pentylformic acid

1-pentanecarboxylate

Butylacetic acid

Pentiformic acid

Capronic acid

HEXANOIC ACID

Caproic acid

Hexoic acid

Hexylic acid

1-Pentanecarboxylic acid

5-carboxypentyl

hexansäure

n-caproate

n-hexoate

n-hexylate

AC1Q2VOK

Hexanoic acid Caproic acid

Hexanoic acid, analytical standard

Nat.Hexanoic Acid

1-hexanoate

ACMC-1BTHO

n-Caproic acid

n-Hexanoic acid

n-Hexylic acid

n-Hexoic acid

1-Hexanoic acid

AC1L1RW7

Acid C6

Pentane-1-carboxylic acid

Kyselina kapronova [Czech]

methyl 5-pentanoic acid

SCHEMBL3867

ethyl 4-butanoic acid

KSC177A6N

M557

CHEMBL14184

Hexacid 698

Hexanoic acid (natural)

NSC8266

UN2829

1F8SN134MX

BDBM16433

C6:0

CTK0H7066

HMDB00535

WLN: QV5

hexanoic acid (caproic acid)

Hexanoic acid, >=99%

RP19238

5-Carboxypentyl-Sepharose® 4B N-succinimidyl ester

bmse000351

C01585

CCRIS 1347

CH3(CH2)4COOH

Hexanoic acid, 99%

HSDB 6813

UNII-1F8SN134MX

AN-1410

DTXSID7021607

LP071647

LP097943

LS-2796

NSC 8266

NSC-8266

SBB053586

(C6-C12)Alkylcarboxylic acid

CHEBI:30776

DSSTox_CID_1607

Fatty Acid 1210

ZINC1529230

ANW-20709

DSSTox_GSID_21607

HEXANOIC ACID (CAPROIC ACID)

TRA0069554

DSSTox_RID_76233

LMFA01010006

MFCD00004421

AI3-07701

NCIOpen2_005355

RTR-035704

ST51046281

TR-035704

(C5-C9) Monobasic acids

(C6-C12) Alkylcarboxylic acid

AKOS000119844

I04-1053

J-007673

BRN 0773837

FEMA No. 2559

FT-0659402

C6:0 (Lipid numbers)

CH3-[CH2]4-COOH

Z955123566

Tox21_201517

Tox21_300406

142-62-1

Hexanoic acid, natural, >=98%, FCC

8040-17-3

Hexanoic acid, >=98%, FCC, FG

MCULE-1671810139

NCGC00248020-01

NCGC00248020-02

NCGC00254504-01

NCGC00259067-01

CAS-142-62-1

EINECS 205-550-7

EINECS 267-013-3

EINECS 271-676-4

EINECS 274-509-3

51109-46-7

53896-26-7

68603-84-9

70248-25-8

Caproic acid [UN2829] [Corrosive]

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

MolPort-001-769-761

11034-EP2269610A2

11034-EP2270002A1

11034-EP2277848A1

11034-EP2284146A2

11034-EP2284147A2

11034-EP2289510A1

11034-EP2298313A1

11034-EP2316457A1

11034-EP2316458A1

11034-EP2316825A1

11034-EP2316826A1

11034-EP2316827A1

11034-EP2316828A1

16407-EP2275401A1

16407-EP2281563A1

16407-EP2284160A1

16407-EP2289890A1

16407-EP2305646A1

16407-EP2305687A1

16407-EP2311824A1

16407-EP2311842A2

16407-EP2316459A1

16407-EP2374787A1

16420-EP2275401A1

16420-EP2281563A1

16420-EP2289890A1

16420-EP2305646A1

16420-EP2311842A2

16420-EP2316459A1

Caproic acid [UN2829] [Corrosive]

Hexanoic acid, purum, >=98.0% (GC)

19455-00-6 (potassium salt)

10051-44-2 (sodium salt)

38708-95-1 (calcium salt)

4-02-00-00917 (Beilstein Handbook Reference)

25401AB4-1ECB-481F-AC91-EAAFC9329BDD

16571-42-9 (manganese(2+) salt)

13476-79-4 (copper(2+) salt)

Carboxylic acids, C6-18 and C6-18-unsatd. mono- and C8-15-di-

InChI=1/C6H12O2/c1-2-3-4-5-6(7)8/h2-5H2,1H3,(H,7,8

The pKa of hexanoic acid is 4.88(1), indicating that this compound will exist predominantly as an anion under environmental conditions. Volatilization will not occur from water and moist soils since anions do not volatilize(SRC). Hexanoic acid is not expected to volatilize from dry soil surfaces(SRC), based upon an extrapolated vapor pressure of 0.0435 mm Hg at 25 deg C(2).
Literature: (1) Riddick, JA et al;. Techniques of Chemistry 4th ed Volume II. Organic Solvents. New York, NY: John Wiley and Sons, pp 372 (1985)(2) Daubert TE, Danner RP; Physical & Thermodynamic Properties of Pure Chemicals: Data Compilation, NY: Hemisphere Pub Corp (1989)

Koc values of 26, 24 and 37 have been experimentally measured, for an acidic forest soil (pH 2.8, 4.85% organic carbon), agricultural soil (pH 6.7, 1.25% organic carbon), and a lake sediment (pH 7.1, 1.58% organic carbon), respectively(1). According to a classification scheme(2), these measured Koc values suggest that hexanoic acid is very highly mobile in soil(SRC). In addition, the pKa of hexanoic acid is 4.88(3), indicating that this compound will primarily exist as an anion in the environment, and anions generally possess high mobility in soil(4).
Literature: (1) Von Oepen B et al; Chemosphere 22: 285-304 (1991) (2) Swann RL et al; Res Rev 85: 23 (1983) (3) Riddick, JA et al;. Techniques of Chemistry 4th ed Volume II. Organic Solvents. New York, NY: John Wiley and Sons, pp 372 (1985) (4) Doucette WJ; pp. 141-188 in Handbook of Property Estimation Methods for Chemicals. Boethling RS, Mackay D, eds. Boca Raton, FL: Lewis Publ (2000)

Myristinsaeure

Tetradecanoate

tridecanecarboxylic acid

acide tetradecanoique

myristoate

n-Tetradecanoicacid

1-Tridecanecarboxylate

Crodacid

Myristate

Tetradecanoic acid

TUNFSRHWOTWDNC-UHFFFAOYSA-N

n-Tetradecanoate

tetradecoic acid

1-tetradecanecarboxylic acid

MYRISTIC ACID

myristoic acid

1-Tridecanecarboxylic acid

n-Tetradecanoic acid

Myristic Acid Flake

Myristic acid pure

n-Tetradecoic acid

3usx

Myristic acid, analytical standard

ACMC-1AKMJ

n-Myristic acid

3v2n

3w9k

Myristic acid, natural

AC1L1WF8

AC1Q2W1A

Myristic acid, pure

Tetradecanoic (Myristic) acid

SCHEMBL6374

AC1Q2W11

GTPL2806

KSC271K5J

s161

C14 fatty acid

Myristic acid (natural)

Myristic acid, puriss.

n-tetradecan-1-oate

NSC5028

0I3V7S25AW

CTK1H1554

Emery 655

HMDB00806

Hystrene 9014

Hystrene 9514

Kortacid 1499

M0476

Myristic Acid 655

Myristic acid, pharmaceutical secondary standard; traceable to USP

Philacid 1400

CHEMBL111077

DB08231

Edenor C 14

LS-210

Myristic acid [NF]

n-Tetradecan-1-oic acid

NE10225

Neo-fat 14

Prifac 2942

Prifrac 2942

Tetradecanoic acid (9CI)

bmse000737

C06424

C14:0

CCRIS 4724

HMS3039E15

HMS3648O20

HSDB 5686

Hydrofol acid 1495

Myristic acid, 95%

UNII-0I3V7S25AW

Univol U 316S

WLN: QV13

AK114664

BT000309

DTXSID6021666

LP003932

Myristic acid (8CI)

NSC 5028

NSC-5028

SBB060024

ST023797

CHEBI:28875

DSSTox_CID_1666

Myristic acid, United States Pharmacopeia (USP) Reference Standard

ZINC1530417

AB1002562

AN-21363

ANW-32091

DSSTox_GSID_21666

BDBM50147581

DSSTox_RID_76274

LMFA01010014

MFCD00002744

AI3-15381

KB-260944

RTR-019260

ST24025989

TR-019260

AKOS009156714

Epitope ID:176772

I04-0252

Myristic acid, Sigma Grade, >=99%

W-109088

BRN 0508624

FEMA No. 2764

FT-0602832

MLS002152942

SMR001224536

EN300-78099

Tox21_201852

Tox21_302781

544-63-8

C14:0 (Lipid numbers)

CH3-[CH2]12-COOH

F8889-5016

MCULE-9671122893

Myristic acid, >=95%, FCC, FG

NCGC00091068-01

NCGC00091068-02

NCGC00091068-03

NCGC00256547-01

NCGC00259401-01

CAS-544-63-8

EINECS 208-875-2

EINECS 250-924-5

45184-05-2

Myristic acid, Vetec(TM) reagent grade, 98%

Myristic acid, >=98.0% (GC)

MolPort-001-779-744

4-02-00-01126 (Beilstein Handbook Reference)

EDAE4876-C383-4AD4-A419-10C0550931DB

A pKa of 4.90(1) indicates myristic 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). Myristic acid is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 1.4X10-6 mm Hg(3).
Literature: (1) Barratt MD; Toxicol In Vitro 10:85-94 (1996) (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 Domination. Design Inst Phys Prop Data, Amer Inst Chem Eng. NY, NY: Hemisphere Pub. Corp 4 Vol (1989)

The Koc of myristic acid is estimated as 50,000 fro the free acid(SRC), using a log Kow of 6.11(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that undissociated myristic acid is expected to be immobile in soil. The pKa of myristic acid is 4.90(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) Barratt MD; Toxicol In Vitro 10:85-94 (1996) (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)