pentadecanecarboxylate

Pentadecanecarboxylic acid

Palmitinsaeure

Palmiticacid

Hexadecoate

Palmitinate

palmitoate

Calcium palmitate

Hexadecanoic acid

Hydrofol

IPCSVZSSVZVIGE-UHFFFAOYSA-N

palmitate

hexadecoic acid

Hexadecylic acid

hexaectylic acid

Palmitinic acid

1-Pentadecanecarboxylic acid

Hexadecanoic acid anion

Hexadecanoic acid Palmitic acid

n-hexadecoate

palmitic acid

palmitoic acid

1-hexyldecanoate

Cetylic acid

FAT

palmic acid

Palmitic acid_RaGuSa

PLM

Fatty acid pathway

n-Hexadecanoic acid

Palmitic acid_jeyam

2hmb

2hnx

n-Hexadecoic acid

Palmitic acid, analytical standard

1-Hexyldecanoic Acid

ACMC-1ASQF

3v2q

AC1L1AH2

Palmitic acid, pure

Edenor C16

SCHEMBL6177

1b56

GTPL1055

I728

KSC270O2R

Palmitic acid 95%

C16 fatty acid

CHEMBL82293

Emersol 140

Emersol 143

Industrene 4516

NSC5030

Palmitic acid (natural)

Pristerene 4934

Univol U332

CTK1H0728

HMDB00220

Hystrene 8016

Hystrene 9016

Kortacid 1695

Kortacid 1698

Lunac P 95KC

N2456

P0002

P1145

QSPL 166

DB03796

Glycon P-45

Hexadecanoic acid (9CI)

Lunac P 95

Lunac P 98

P5585_SIGMA

PA 900

Palmitic acid (NF)

Palmitic acid, >=99%

Prifac 2960

Prifrac 2960

RP29137

2V16EO95H1

bmse000590

C00249

C16:0

CCRIS 5443

D05341

HMS3649N08

HSDB 5001

Hydrofol Acid 1690

Loxiol EP 278

Palmitic acid, European Pharmacopoeia (EP) Reference Standard

WLN: QV15

BBL011563

DNC005038

DTXSID2021602

FA 1695

LP002534

LS-2331

NSC 5030

NSC-5030

Palmitic acid [USAN:NF]

SBB017229

ST023798

STL146733

CHEBI:15756

DSSTox_CID_1602

Palmitic acid, certified reference material, TraceCERT(R)

Palmitic acid, pharmaceutical secondary standard; traceable to USP and PhEur

Palmitic acid, United States Pharmacopeia (USP) Reference Standard

UNII-2V16EO95H1

ZINC6072466

AB1002597

AK-48351

AN-23574

ANW-13574

DSSTox_GSID_21602

Palmitic acid, BioXtra, >=99%

SC-81752

(C14-C18)Alkylcarboxylic acid

BB_SC-9400

BDBM50152850

DSSTox_RID_76229

LMFA01010001

MFCD00002747

AI3-01594

RTC-060456

SEL10404124

ST24025707

TC-060456

AKOS005720983

BB_SC-09400

Epitope ID:141181

Palmitic acid (7CI,8CI)

S04-0102

BRN 0607489

FEMA No. 2832

FT-0626965

(C14-C18) Alkylcarboxylic acid

57-10-3

Palmitic acid, Grade II, ~95%

Z955123552

Fatty acids, C14-18

Tox21_112105

Tox21_201671

Tox21_302966

C16:0 (Lipid numbers)

CH3-[CH2]14-COOH

CAS-57-10-3

Palmitic acid, natural, 98%, FG

8045-38-3

MCULE-1361949901

NCGC00164358-01

NCGC00164358-02

NCGC00164358-03

NCGC00256424-01

NCGC00259220-01

Palmitic acid, >=95%, FCC, FG

Palmitic acid, for synthesis, 98.0%

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

EINECS 200-312-9

EINECS 266-926-4

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

Palmitic acid, 95% 500g

60605-23-4

66321-94-6

67701-02-4

Palmitic acid, SAJ first grade, >=95.0%

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

SDA 17-005-00

SR-01000944716

Tox21_112105_1

116860-99-2

212625-86-0

MolPort-001-780-241

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

SR-01000944716-1

Light end (C14-C18) saturated fatty acid fraction from tallow fatty acids

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

BA71C79B-C9B1-451A-A5BE-B480B5CC7D0C

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)

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)

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)

beta-hydroxymyristicacid

beta-Hydroxytetradecanoic acid

ATRNZOYKSNPPBF-UHFFFAOYSA-N

DL-B-HYDROXYMYRISTICACID

beta-Hydroxymyristic acid

3-HYDROXYTETRADECANOIC ACID

3-hydroxy-tetradecanoicaci

DL-beta-Hydroxymyristic acid

Z6X

DL-B-HYDROXYMYRISTIC ACID

3-Hydroxymyristic acid

3-HYDROXY-TETRADECANOIC ACID

ACMC-1CSHD

.beta.-Hydroxytetradecanoic acid

.beta.-Hydroxymyristic acid

AC1L276O

CTK8B1115

(RS)-3-Hydroxytetradecanoic acid

SCHEMBL142895

3-Hydroxymyristic acid (racemic)

DL-beta-Hydroxymyristic acid, >=98%

Tetradecanoic acid, 3-hydroxy-

(r)-3-hydroxytetradeconoic acid

LP002052

AK392274

(3RS)-3-Hydroxytetradecanoic acid

R-(3)-HYDROXYMYRISTIC ACID

CHEBI:85148

ANW-23709

AN-50149

ACM3422319

ACM1961724

C-44473

MFCD00059633

LMFA01050175

TC-112454

( inverted exclamation markA)-3-hydroxyteradecanoic acid

LS-148904

AKOS027380549

J-019508

hydroxymyristic acid, 3-(sg)

FT-0625445

FT-0615850

FT-0080015

BRN 1725372

3-hydroxymyristic acid, (ss-)

1961-72-4

3422-31-9

(+/-)-3-Hydroxytetradecanoic acid

28715-21-1

3-hydroxymyristic acid (beta-) 96+%

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

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

F98D6745-6EF1-4182-BB79-6FB77737B72C

hexadecenoicacid

ZVRMGCSSSYZGSM-CCEZHUSRSA-N

Hexadecenoic acid

2-HEXADECENOICACID

cis-Hexadecenoic acid

Gaidic acid

AC1NR0PC

2-hexadecenoic acid

2-palmitoleic acid

trans-2-Hexadecenoic acid

2-trans-hexadecenoic acid

2-Hexadecenoic acid, AldrichCPR

t-2-hexadecenoic acid

HMDB10735

trans-hexadec-2-enoic acid

SCHEMBL189080

trans-Delta(2)-hexadecenoic acid

(2E)-hexadecenoic acid

LP082453

DTXSID1075014

AK167091

CHEBI:37252

Trans-Hexa-dec-2-enoic acid

TL8004329

LMFA01030054

(E)-2-hexadecenoic acid

MFCD00045907

ZINC32838989

C-49182

Caswell No. 481

t-16:1D2

TR-021668

AKOS015839097

EPA Pesticide Chemical Code 045401

C16:1n-14

FT-0632664

(E)-hexadec-2-enoic acid

(2E)-2-Hexadecenoic acid #

629-56-1

I14-107536

(2E)-hexadec-2-enoic acid

25447-95-4

10B54E76-29DB-4830-BC82-772EB20A8FEB