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)

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)

ANTEISOPENTADECANOIC ACID

12-Methyltetradecansaeure

Sarcinic acid

Aseanostatin P5

12-Methyl-tetradecansaeure

12-Methyltetradecanoic acid

AC1L2ITY

anteiso-C15

12-Methyl tetradecanoic acid

12-methyl-tetradecanoic acid

12-MTA

CTK8J2149

SCHEMBL397325

CHEMBL495852

C15:0ai

aC15:0

15:0ai

anteiso-C15:0

a15:0

C16665

HMS2267L13

anteiso-15:0

LP072281

15:0 anteiso

CHEBI:39251

KB-64806

Tetradecanoic acid, 12-methyl-

C-55310

LMFA01020008

MFCD00083664

12-Methyltetradecanoic acid; Sarcinic acid; Aseanostatin P5

MLS000517264

(+)-12-Methyltetradecanoic acid

SMR000127417

5502-94-3

NCGC00247048-01

(+)-12-methyl myristic acid

Isotridecanoic acid

SIOLDWZBFABPJU-UHFFFAOYSA-N

Isoundecylic acid

11-METHYLDODECANOICACID

AC1L1OTN

11-Methyldodecanoic acid

11-methyllauric acid

11-methyl-dodecanoic acid

CTK4F5765

SCHEMBL809936

i13:0

DTXSID1067099

LP001201

C13:0 iso

CHEBI:77359

iso-C13:0

ZINC2013445

AN-17760

13:0 iso

C-49845

MFCD00044078

LMFA01020006

DB-052971

11-Methyllauric acid, >=98%

ACM25448242

W-110634

FT-0635805

5681-98-1

EINECS 246-997-8

25448-24-2

79548-60-0

26403-18-9

isopentadecanoicacid

Subtilopentadecanoic acid

Isopentadecanoic acid

Isopentadecylic acid

ZOCYQVNGROEVLU-UHFFFAOYSA-N

13-METHYLTETRADECANOICACID

13-Methyl-tetradecansaeure

13-Methylmyristate

13-Methyltetradecanoic acid

13-methylmyristic acid

AC1L45HO

13-methyl-tetradecanoic acid

M09T9M1LTY

13-Methyl tetradecanoic acid

iso-C15

13-Mtd

UNII-M09T9M1LTY

Isopentadecanoic acid(7CI,9CI)

CTK1A1122

SCHEMBL366393

CHEMBL495851

LP001111

iso-C15:0

ZINC1911381

CHEBI:39250

i-C15:0

DTXSID90179552

15:0 iso

Tetradecanoic acid, 13-methyl-

KB-64810

i-15:0

LMFA01020009

C-55238

MFCD00083431

ACM50973096

J-015704

2485-71-4

13-Methylmyristic acid, >=98% (capillary GC)

27836-87-9

50973-09-6

3-Hmhd

AC1L4PJ0

AC1Q1PD0

3-Hydroxy-15-methylhexadecanoate

3-hydroxy-15-methylhexadecanoic acid

CTK4F5913

LP109165

SCHEMBL1358207

Hexadecanoic acid,3-hydroxy-15-methyl-

Hexadecanoic acid, 3-hydroxy-15-methyl-

25491-28-5

3-hydroxypentadecanoic acid

3-hydroxy-pentadecanoic acid

AC1L4A9W

Pentadecanoic acid,3-hydroxy-

CTK4G8995

SCHEMBL311217

AK401943

LP001216

LMFA01050183

MFCD00210306

ACM32602703

AKOS027383861

32602-70-3

3-HYDROXYHEXADECANOICACID

beta-Hydroxyhexadecanoic acid

CBWALJHXHCJYTE-UHFFFAOYSA-N

beta-Hydroxypalmitic acid

3-hydroxyhexadecanoic acid

DL-beta-Hydroxypalmitic acid

3-Hydroxypalmitic acid

AC1L6YRF

DL--Hydroxypalmitic acid

3-hydroxy-hexadecanoic acid

Hexadecanoic acid,3-hydroxy-

CTK4F2704

DL-.beta.-Hydroxypalmitic acid

SCHEMBL310976

DL-beta-Hydroxypalmitic acid, >=98%

AK401023

Hexadecanoic acid, 3-hydroxy-

LP038560

NSC179484

CHEBI:37248

CC-15318

C-17167

LMFA01050188

MFCD00171638

DB-057332

NSC-179484

AKOS024438254

FT-0633110

928-17-6

2398-34-7

20595-04-4

A9897684-CABA-4D85-8749-EF6BF75EB0A0