3-hydroxyhexadecanoic acid

2398-34-7

3-hydroxy-hexadecanoic acid

928-17-6

3-Hydroxypalmitic acid

Hexadecanoic acid,3-hydroxy-

beta-Hydroxyhexadecanoic acid

DL-beta-Hydroxypalmitic acid

Hexadecanoic acid, 3-hydroxy-

3-HYDROXYHEXADECANOICACID

20595-04-4

beta-Hydroxypalmitic acid

MFCD00171638

Hexadecanoic acid, 3-hydroxy-, (A+/-)-

3-?Hydroxy-hexadecanoic Acid

DL-(2)-Hydroxypalmitic acid

SCHEMBL310976

DL- beta -Hydroxypalmitic acid

DL-.beta.-Hydroxypalmitic acid

CHEBI:37248

?-HYDROXYHEXADECANOIC ACID

DTXSID80946831

(+/-)-3-hydroxyhexadecanoic acid

CAA39834

LMFA01050188

NSC179484

AKOS024438254

DL-beta-Hydroxypalmitic acid, >=98%

NSC-179484

AS-59627

BP-29862

PD044275

DB-057332

F87673

A929893

Q27117078

A9897684-CABA-4D85-8749-EF6BF75EB0A0

hexadec-2-enoic acid

hexadecaenoic acid

ZVRMGCSSSYZGSM-UHFFFAOYSA-N

DTXSID001347916

AKOS028110148

PD118471

DB-054346

Tetradecanoic acid

MYRISTIC ACID

544-63-8

n-Tetradecanoic acid

Crodacid

n-Tetradecan-1-oic acid

n-Tetradecoic acid

1-Tridecanecarboxylic acid

Myristate

Hydrofol acid 1495

Myristinsaeure

Univol U 316S

Emery 655

tetradecoic acid

Hystrene 9014

Myristic acid, pure

FEMA No. 2764

Myristic acid (natural)

acide tetradecanoique

n-Myristic acid

NSC 5028

CCRIS 4724

HSDB 5686

Philacid 1400

C14:0

Prifac 2942

CH3-[CH2]12-COOH

CHEBI:28875

AI3-15381

NSC-5028

1-tetradecanecarboxylic acid

EINECS 208-875-2

PHILACID-1400

UNII-0I3V7S25AW

PRIFRAC-2942

BRN 0508624

0I3V7S25AW

DTXSID6021666

Edenor C 14

Acid, Myristic

MyristicAcid-13C14

CHEMBL111077

DTXCID501666

MYRISTIC-14-13C ACID

NSC5028

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

MFCD00002744

FA 14:0

n-tetradecan-1-oate

MYRISTIC ACID (II)

MYRISTIC ACID [II]

32112-52-0

MYRISTIC ACID (MART.)

MYRISTIC ACID [MART.]

MYRISTIC ACID (USP-RS)

MYRISTIC ACID [USP-RS]

CH3-(CH2)12-COOH

CAS-544-63-8

Acid, Tetradecanoic

Myristic acid [NF]

62217-70-3

myristoate

myristoic acid

n-Tetradecanoate

Tetradecanoicacid

3usx

Myristic acid pure

fatty acid 14:0

Hystrene 9514

TETRADECANSAEURE

1-Tridecanecarboxylate

ACIDO MYNISTICO

MAGNESIUMARSENATE

Myristic acid, 95%

Myristic acid, natural

tridecanecarboxylic acid

Myristic acid (8CI)

Myristic Acid, Reagent

3v2n

3w9k

Myristic acid, puriss.

Univol U 3165

Myristic acid, ?99%

Tetradecanoic acid (9CI)

bmse000737

Epitope ID:176772

MYRISTIC ACID [MI]

SCHEMBL6374

MYRISTIC ACID [FCC]

MYRISTIC ACID [FHFI]

MYRISTIC ACID [HSDB]

MYRISTIC ACID [INCI]

MLS002152942

WLN: QV13

Tetradecanoic (Myristic) acid

GTPL2806

NAA 104

NAA 142

IS_D27-TETRADECANOIC ACID

HMS3039E15

HMS3648O20

Myristic acid, analytical standard

HY-N2041

EINECS 250-924-5

Myristic acid, >=98.0% (GC)

Tox21_201852

Tox21_302781

BDBM50147581

LMFA01010014

s5617

STL185697

Myristic acid, >=95%, FCC, FG

Myristic acid, Sigma Grade, >=99%

AKOS009156714

CCG-266785

DB08231

DS-3833

MCULE-9671122893

NSC 122834

NCGC00091068-01

NCGC00091068-02

NCGC00091068-03

NCGC00256547-01

NCGC00259401-01

AC-34674

BP-27915

SMR001224536

CS-0018531

M0476

NS00010444

EN300-78099

C06424

G74510

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

Q422658

SR-01000854525

MYRISTIC ACID (CONSTITUENT OF SAW PALMETTO)

SR-01000854525-3

W-109088

F8889-5016

Z1954802504

EDAE4876-C383-4AD4-A419-10C0550931DB

MYRISTIC ACID (CONSTITUENT OF SAW PALMETTO) [DSC]

Myristic acid, United States Pharmacopeia (USP) Reference Standard

Tetradecanoic acid; 1-Tridecanecarboxylic acid; n-Tetradecanoic acid

Myristic acid, Pharmaceutical Secondary Standard; Certified Reference Material

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)

stearic acid

Octadecanoic acid

57-11-4

n-Octadecanoic acid

Stearophanic acid

Cetylacetic acid

1-Heptadecanecarboxylic acid

Pearl stearic

Stearex Beads

Octadecansaeure

Stearinsaeure

Vanicol

Hydrofol Acid 150

Century 1240

Glycon DP

Glycon TP

Industrene R

Stearate

Formula 300

Hydrofol 1895

Hystrene 7018

Hystrene 9718

Glycon S-80

Glycon S-90

octadecoic acid

Tegostearic 254

Tegostearic 255

Tegostearic 272

Hystrene 80

Humko Industrene R

Hydrofol acid 1655

Hydrofol acid 1855

Hystrene S-97

Hystrene T-70

Industrene 5016

Dar-chem 14

Emersol 120

Emersol 132

Hystrene 4516

Hystrene 5016

Groco 54

Groco 55

Groco 55L

Groco 58

Groco 59

Glycon S-70

Industrene 8718

Industrene 9018

Emersol 150

Kam 1000

Barolub FTA

FEMA No. 3035

Acidum stearinicul

C18:0

Caswell No. 801D

Oktadekansaeure

HY-Phi 1199

HY-Phi 1205

HY-Phi 1303

HY-Phi 1401

acide stearique

Kam 2000

Kam 3000

Steric acid

Century 1210

acide octadecanoique

Stearic acid, pure

PD 185

NAA 173

CCRIS 2305

Stearic acid 50

HSDB 2000

Emersol 153NF

Dervacid 3155

Purified stearic acid

Adeka sa 300

Century 1220

Century 1230

Emersol 6349

Hydrofol Acid 150 (VAN)

NSC 25956

Lunac S 40

Hydrofol Acid 1895

Prifac 2918

Promulsin

EPA Pesticide Chemical Code 079082

Vis-Plus

AI3-00909

UNII-4ELV7Z65AP

EINECS 200-313-4

n-Octadecylic acid

4ELV7Z65AP

NSC-25956

Pristerene 4900

Hystrene S 97

Hystrene T 70

Stearic Acid Cherry

Edenor C18

Edenor ST 1

Sunfat 18S

BRN 0608585

Emersol 153

Selosol 920

Stearic acid (TN)

Hystrene 9718NF

Kortacid 1895

Lunac 30

CH3-[CH2]16-COOH

DTXSID8021642

Loxiol G 20

CHEBI:28842

Lunac S 20

Lunac S 30

Lunac S 90

Lunac S 90KC

Hystrene 9718NFFG

MFCD00002752

NSC-261168

CHEMBL46403

17FA

DTXCID301642

EC 200-313-4

4-02-00-01206 (Beilstein Handbook Reference)

NSC25956

FA 18:0

NCGC00091596-02

STEARIC ACID (II)

STEARIC ACID [II]

400JB9103-88

A 1760

68937-76-8

STEARIC ACID (MART.)

STEARIC ACID [MART.]

STEARIC ACID (USP-RS)

STEARIC ACID [USP-RS]

CH3-(CH2)16-COOH

Oktadekansaure

Stearicacid

Lunac

STEARIC ACID (EP MONOGRAPH)

STEARIC ACID [EP MONOGRAPH]

CAS-57-11-4

Isostearic acid EX

Haimaric MKH(R)

Prisorine 3501

Prisorine 3502

Prisorine 3508

Emersol 871

Emersol 875

Emery 875D

Emery 871

Unimac 5680

C-Lube 10

Stearic acid [JAN:NF]

octadecansaure

Stearinsaure

Stearophanate

Stearex

Tsubaki

n-Octadecanoate

Bassinic acid

Lactaric acid

Talgic acid

Doctor Plus

Edenor htict-n

1hmr

1hmt

4fnn

Kiri stearic acid

Obeo Baby Bubble

Jinhwagwangsu Hair

Lunac YA

Palmitostearic acid

Stearic acid 70

Stearic acid, CP

Sterene 60b

Sterene 60r

EINECS 250-178-0

F 3 (lubricant)

Industrene 4518

Jinhwagwangsu Bubble

Nonsoul SK 1

Pristerene 4904

Pristerene 4910

Pristerene 4916

Pristerene 4963

Pristerene 4981

Pristerene 9429

Pristerene 9559

Pristerine 4989

CELOZOLE

fatty acid 18:0

Sterene 460

Industrene 5016K

Radiacid 0427

Edenor ST 20

Serfax MT 90

Stearic acid_ravikumar

Unister NAA 180

Century 1224

NORSOREX AP

Edenor HT-JG 60

Stearic acid (8CI)

Stearic acid, puriss.

Hyfac 410

Hyfac 420

Hyfac 421

Hyfac 422

Hystrene 7018 FG

Lunac S 50

Lunac S 98

Prifac 5905

3v2p

875D

1-Heptadecanecarboxylate

Industrene 7018 FG

AFCO-Chem B 65

Heptadecanecarboxylic acid

Edenor C 18/98

Octadecanoic acid (9CI)

Stearic acid, >=98%

SCHEMBL659

Hystrene 9718 NF FG

bmse000485

STEARIC ACID [MI]

Emery 400 (Salt/Mix)

NEO-FAT 18S

STEARIC ACID [DSC]

STEARIC ACID [JAN]

Stearic acid (JP15/NF)

Stearic acid (JP17/NF)

Emersol 110 (Salt/Mix)

STEARIC ACID [FHFI]

STEARIC ACID [HSDB]

STEARIC ACID [INCI]

NOPCOCERA LU 6418

Stearic acid (reagent grade)

STEARIC ACID [VANDF]

WLN: QV17

STEARIC ACID [WHO-DD]

GTPL3377

WO 2

UNII-X33R8U0062

CELLBN FIRST CARE CLEANSER

NAA 180

Nonsoul SN 1 (*Sodium salt*)

SNA-2000 (*Sodium salt*)

Stearic acid, analytical standard

VLZ 200

S 30C

PURIFIED STEARIC ACID [NF]

Stearic acid, reagent grade, 95%

HY-B2219

ZENOL POWERFULX RECOVERYCREAM

Tox21_111154

Tox21_201887

Tox21_300562

BBL012224

BDBM50240485

LMFA01010018

s5733

SA 200

Stearic acid, >=95%, FCC, FG

STL163565

AKOS005716958

Tox21_111154_1

CCG-267314

DB03193

FA 1655

MCULE-5127577640

NSC 261168

X33R8U0062

NCGC00091596-01

NCGC00091596-03

NCGC00091596-04

NCGC00091596-05

NCGC00254456-01

NCGC00259436-01

E570

VS-03242

Stearic acid, puriss., >=98.5% (GC)

Stearic acid, SAJ first grade, >=90.0%

CS-0021598

G 270

NS00010335

S 300

S0163

EN300-19730

Stearic acid, SAJ special grade, >=95.0%

Stearic acid, Vetec(TM) reagent grade, 94%

C01530

D00119

EC 250-178-0

F70008

Stearic acid 50, tested according to Ph.Eur.

Q209685

SR-01000944717

STEARIC ACID (CONSTITUENT OF SAW PALMETTO)

Melting Point Standard 69-71C, analytical standard

SR-01000944717-1

Stearic acid, Grade I, >=98.5% (capillary GC)

Stearic acid, SAJ first grade, >=90.0%, powder

F0001-1489

STEARIC ACID (CONSTITUENT OF SAW PALMETTO) [DSC]

Stearic acid, certified reference material, TraceCERT(R)

Z104474964

CD7993EA-AD14-452A-A907-33376CC98790

Stearic acid, European Pharmacopoeia (EP) Reference Standard

Stearic acid, United States Pharmacopeia (USP) Reference Standard

Stearic Acid, Pharmaceutical Secondary Standard; Certified Reference Material

18639-67-3

InChI=1/C18H36O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h2-17H2,1H3,(H,19,20

An estimated pKa of 4.7(1) indicates stearic 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). Stearic acid is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 4.3X10-8 mm Hg at 25 deg C(3).
Literature: (1) SPARC; pKa/property server. Ver 3. Jan, 2006. Available at http://ibmlc2.chem.uga.edu/sparc/ as of Mar 5, 2008. (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 undissociated stearic acid is estimated as 710,000(SRC), using a log Kow of 8.23(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that undissociated stearic acid is expected to be immobile in soil. The estimated pKa of stearic acid is 4.75(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). However, the adsorption of stearate, the anion of stearic acid, was determined using relatively nonpolar marine sediment sand surfaces: anoxic clastic mud from Cape Lookout Bight, NC (3.5 g/g organic carbon, clay), fine carbonate beach sand from Kahana Stream, Oahu, HI (1.3 g/g organic carbon, fine sand and silty clay), and a fine carbonate sand from Waimanalo Beach, Oahu, HI (0.17 g/g organic carbon, fine-very fein sand)(6) Stearate exhibited Kds of 210, 140 and 36, respectively; overall averaging 99% adsorption(6).
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) SPARC; pKa/property server. Ver 3. Jan, 2006. Available at http://ibmlc2.chem.uga.edu/sparc/ as of Mar 5, 2008. (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) (6) Sansone FJ et al; Geochimica et Cosmochimica Acta 51: 1889-96 (1987)

lauric acid

DODECANOIC ACID

143-07-7

n-Dodecanoic acid

Dodecylic acid

Vulvic acid

Laurostearic acid

Dodecoic acid

Duodecylic acid

1-Undecanecarboxylic acid

Aliphat No. 4

Ninol AA62 Extra

Wecoline 1295

Hydrofol acid 1255

Hydrofol acid 1295

Duodecyclic acid

Hystrene 9512

Univol U-314

Lauric acid, pure

Dodecylcarboxylate

Lauric acid (natural)

Laurinsaeure

Undecane-1-carboxylic acid

ABL

NSC-5026

FEMA No. 2614

laurate

C-1297

Philacid 1200

CCRIS 669

C12:0

Emery 651

Lunac L 70

CHEBI:30805

HSDB 6814

EINECS 205-582-1

UNII-1160N9NU9U

BRN 1099477

n-Dodecanoate

Kortacid 1299

Dodecanoic Acid Anion

DTXSID5021590

Prifrac 2920

AI3-00112

Lunac L 98

Univol U 314

Prifac 2920

1160N9NU9U

MFCD00002736

DAO

DTXCID801590

CH3-[CH2]10-COOH

NSC5026

EC 205-582-1

dodecylate

laurostearate

vulvate

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

DODECANOIC ACID (LAURIC ACID)

1-undecanecarboxylate

LAURIC ACID (USP-RS)

LAURIC ACID [USP-RS]

CH3-(CH2)10-COOH

8000-62-2

CAS-143-07-7

SMR001253907

laurinsaure

dodecanic acid

Nuvail

lauric-acid

Acide Laurique

n-Dodecanoicacid

3uil

Lauric acid (NF)

DODECANOICACID

fatty acid 12:0

Lauric Acid, Reagent

Nissan NAA 122

Emery 650

Dodecanoic acid, 98%

Dodecanoic acid, 99%

Guaranteed Reagent,99%

Dodecanoic (Lauric) acid

LAURIC ACID [MI]

bmse000509

LAURIC ACID [FCC]

LAURIC ACID [FHFI]

LAURIC ACID [INCI]

SCHEMBL5895

NCIOpen2_009480

MLS002177807

MLS002415737

WLN: QV11

Dodecanoic acid (lauric acid)

LAURIC ACID [WHO-DD]

Dodecanoic acid, >=99.5%

Edenor C 1298-100

DODECANOIC ACID [HSDB]

CHEMBL108766

GTPL5534

NAA 122

NAA 312

HMS2268C14

HMS3649N06

HY-Y0366

STR08039

Dodecanoic acid, analytical standard

Lauric acid, >=98%, FCC, FG

Tox21_202149

Tox21_303010

BDBM50180948

LMFA01010012

s4726

STL281860

AKOS000277433

CCG-266587

DB03017

FA 12:0

MCULE-2795129925

HYDROFOL ACID 1255 OR 1295

NCGC00090919-01

NCGC00090919-02

NCGC00090919-03

NCGC00256486-01

NCGC00259698-01

AC-16451

BP-27913

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

LAU

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

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

CS-0015078

L0011

NS00008441

EN300-19951

C02679

D10714

A808010

LAURIC ACID (CONSTITUENT OF SAW PALMETTO)

Q422627

SR-01000838338

J-007739

SR-01000838338-3

F0001-0507

LAURIC ACID (CONSTITUENT OF SAW PALMETTO) [DSC]

Z104476194

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

Lauric acid, European Pharmacopoeia (EP) Reference Standard

Lauric acid, United States Pharmacopeia (USP) Reference Standard

Lauric Acid, Pharmaceutical Secondary Standard; Certified Reference Material

203714-07-2

7632-48-6

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)

3-HYDROXYTETRADECANOIC ACID

3-Hydroxymyristic acid

1961-72-4

Tetradecanoic acid, 3-hydroxy-

3422-31-9

beta-Hydroxymyristic acid

DL-B-HYDROXYMYRISTIC ACID

beta-Hydroxytetradecanoic acid

DL-beta-Hydroxymyristic acid

(+/-)-3-hydroxymyristic acid

3-HYDROXY-TETRADECANOIC ACID

FL8S7F2JJQ

.beta.-Hydroxymyristic acid

.beta.-Hydroxytetradecanoic acid

CHEMBL4456892

(RS)-3-Hydroxytetradecanoic acid

(+/-)-3-Hydroxytetradecanoic acid

MFCD00059633

UNII-FL8S7F2JJQ

BRN 1725372

starbld0000280

beta-hydroxy-myristic acid

3-03-00-00660 (Beilstein Handbook Reference)

SCHEMBL142895

DL- beta -Hydroxymyristic acid

CHEBI:85148

3-Hydroxymyristic acid (racemic)

DTXSID20941380

(3RS)-3-Hydroxytetradecanoic acid

BAA96172

BDBM50511033

LMFA01050175

AKOS027380549

CS-W010260

DL-beta-Hydroxymyristic acid, >=98%

HY-W009544

SB47509

AS-58639

3-HYDROXYMYRISTIC ACID, (+/-)-

DB-294356

H0274

T72017

4,6-DINITRO-1,3-BENZENEDICARBONYLCHLORIDE

J-019508

Q27158359

Tetradecanoic acid, 3-hydroxy- (6CI,7CI,8CI,9CI)

F98D6745-6EF1-4182-BB79-6FB77737B72C

Z6X

palmitic acid

Hexadecanoic acid

57-10-3

Cetylic acid

palmitate

n-Hexadecanoic acid

Hexadecylic acid

1-Pentadecanecarboxylic acid

Hydrofol

n-Hexadecoic acid

Palmitinic acid

hexaectylic acid

Pentadecanecarboxylic acid

hexadecoic acid

1-Hexyldecanoic Acid

Industrene 4516

Emersol 140

Emersol 143

Hystrene 8016

Hystrene 9016

Palmitinsaeure

Palmitic acid, pure

Palmitic acid 95%

Kortacid 1698

FEMA No. 2832

Loxiol EP 278

Palmitic acid (natural)

Hydrofol Acid 1690

Cetyl acid

Prifac 2960

C16:0

HSDB 5001

Pristerene 4934

Pristerene-4934

Edenor C16

NSC 5030

AI3-01594

Lunac P 95KC

Lunac P 95

Lunac P 98

CCRIS 5443

Prifac-2960

CHEBI:15756

NSC5030

NSC-5030

EINECS 200-312-9

UNII-2V16EO95H1

FA 16:0

BRN 0607489

Palmitic acid (NF)

DTXSID2021602

Glycon P-45

IMEX C 1498

2V16EO95H1

Hexadecanoic acid (9CI)

MFCD00002747

67701-02-4

Palmitic acid (7CI,8CI)

CHEMBL82293

DTXCID101602

CH3-[CH2]14-COOH

EC 200-312-9

4-02-00-01157 (Beilstein Handbook Reference)

n-hexadecoate

LMFA01010001

PA 900

EDENOR C 16-98-100

FA 1695

SURFAXIN COMPONENT PALMITIC ACID

1-hexyldecanoate

NCGC00164358-01

LUCINACTANT COMPONENT PALMITIC ACID

1219802-61-5

pentadecanecarboxylate

Hexadecanoic acid 10 microg/mL in Acetonitrile

HEXADECANOIC-11,11,12,12-D4 ACID

PALMITIC ACID (II)

PALMITIC ACID [II]

PALMITIC ACID (MART.)

PALMITIC ACID [MART.]

CH3-(CH2)14-COOH

Palmitic acid; Hexadecanoic acid

PLM

palmic acid

Hexadecanoate (n-C16:0)

PALMITIC ACID (EP MONOGRAPH)

PALMITIC ACID [EP MONOGRAPH]

Acid, Palmitic

CAS-57-10-3

Acid, Hexadecanoic

SR-01000944716

Palmitic acid [USAN:NF]

palmitoate

Hexadecoate

Palmitinate

Palmitinsaure

palmitic-acid

palmitoic acid

Hexadecanoicacid

Aethalic acid

Hexadecanoic acid Palmitic acid

2hmb

2hnx

Palmitic acid_jeyam

n-Hexadecyclic Acid

fatty acid 16:0

Palmitic Acid, FCC

Kortacid 1695

Palmitic acid_RaGuSa

Univol U332

Prifrac 2960

Hexadecanoic acid anion

Hexadecanoic--d5 Acid

3v2q

Palmitic acid, >=99%

bmse000590

Epitope ID:141181

CETYL ACID [VANDF]

PALMITIC ACID [MI]

SCHEMBL6177

PALMITIC ACID [DSC]

PALMITIC ACID [FCC]

PALMITIC ACID [FHFI]

PALMITIC ACID [HSDB]

PALMITIC ACID [INCI]

PALMITIC ACID [USAN]

FAT

WLN: QV15

1-MONOPALMITIN_met001

P5585_SIGMA

PALMITIC ACID [VANDF]

GTPL1055

QSPL 166

PALMITIC ACID [USP-RS]

PALMITIC ACID [WHO-DD]

(1(1)(3)C)hexadecanoic acid

1b56

HMS3649N08

Palmitic acid, analytical standard

Palmitic acid, BioXtra, >=99%

Palmitic acid, Grade II, ~95%

HY-N0830

Palmitic acid, natural, 98%, FG

Tox21_112105

Tox21_201671

Tox21_302966

AC9381

BBL011563

BDBM50152850

s3794

STL146733

Palmitic acid, >=95%, FCC, FG

AKOS005720983

Tox21_112105_1

CCG-267027

CR-0047

DB03796

MCULE-1361949901

Palmitic acid, for synthesis, 98.0%

NCGC00164358-02

NCGC00164358-03

NCGC00256424-01

NCGC00259220-01

BP-27917

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

SY006518

CS-0009861

NS00008548

P0002

P1145

Palmitic acid, SAJ first grade, >=95.0%

EN300-19603

C00249

D05341

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

PALMITIC ACID (CONSTITUENT OF SPIRULINA)

Palmitic acid, >=98% palmitic acid basis (GC)

A831313

Q209727

PALMITIC ACID (CONSTITUENT OF FLAX SEED OIL)

PALMITIC ACID (CONSTITUENT OF SAW PALMETTO)

SR-01000944716-1

SR-01000944716-2

BA71C79B-C9B1-451A-A5BE-B480B5CC7D0C

PALMITIC ACID (CONSTITUENT OF BORAGE SEED OIL)

PALMITIC ACID (CONSTITUENT OF SPIRULINA) [DSC]

F0001-1488

Z104474418

PALMITIC ACID (CONSTITUENT OF EVENING PRIMROSE OIL)

PALMITIC ACID (CONSTITUENT OF SAW PALMETTO) [DSC]

Palmitic acid, certified reference material, TraceCERT(R)

Palmitic acid, European Pharmacopoeia (EP) Reference Standard

Palmitic acid, United States Pharmacopeia (USP) Reference Standard

Palmitic acid, Pharmaceutical Secondary Standard; Certified Reference Material

Sodium Palmitate, Palmitic acid sodium salt, Sodium hexadecanoate, Sodium pentadecanecarboxylate, HSDB 759

An estimated pKa of 4.7(1) for palmitic acid indicates palmitic acid will exist almost entirely in the anion form at pH values of 5 to 9 and therefore volatilization from water surfaces is not expected to be an important fate process(2). Palmitic acid is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 3.8X10-7 mm Hg(3).
Literature: (1) SPARC; pKa/property server. Ver 3. Jan, 2006. Available at http://ibmlc2.chem.uga.edu/sparc/ as of Mar 7, 2008. (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 & Thermodynamic Properties of Pure Chemicals 4 NY: Hemisphere Pub Corp (1989)

The Koc of undissociated palmitic acid is estimated as 189,000(SRC), using a log Kow of 7.17(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that undissociated palmitic acid is expected to be immobile in soil. The estimated pKa of palmitic acid is 4.7(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) 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) SPARC; pKa/property server. Ver 3. Jan, 2006. Available at http://ibmlc2.chem.uga.edu/sparc/ as of Mar 7, 2008. (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)