ChemicalBook--->CAS DataBase List--->112-39-0

112-39-0

112-39-0 Structure

112-39-0 Structure
IdentificationMore
[Name]

Methyl hexadecanoate
[CAS]

112-39-0
[Synonyms]

C16
C16:0 METHYL ESTER
HEXADECANOIC ACID METHYL ESTER
METHYL HEXADECANOATE
METHYL N-HEXADECANOATE
METHYL PALMITATE
PALMITIC ACID METHYL ESTER
Emery 2216
Metholene 2216
metholene2216
n-Hexadecanoic acid methyl ester
n-hexadecanoicacidmethylester
Radia 7120
Uniphat A60
uniphata60
METHYL PALMITATE, STANDARD FOR GC
METHYL PALMITATE 97+%
METHYL PALMITATE, 99+%
METHYL PALMITATE OEKANAL
PALMITIC ACID METHYL ESTER 99+%
[EINECS(EC#)]

203-966-3
[Molecular Formula]

C17H34O2
[MDL Number]

MFCD00008994
[Molecular Weight]

270.45
[MOL File]

112-39-0.mol
Chemical PropertiesBack Directory
[Appearance]

Clear colorless liquid or low melting solid
[Melting point ]

32-35 °C (lit.)
[Boiling point ]

185 °C/10 mmHg (lit.)
[density ]

0.852 g/mL at 25 °C(lit.)
[vapor pressure ]

0.008Pa at 25℃
[refractive index ]

n20/D 1.4512(lit.)
[Fp ]

>230 °F
[storage temp. ]

2-8°C
[solubility ]

Chloroform (Sparingly), Methanol (Slightly)
[form ]

Liquid or Low Melting Solid
[color ]

Clear colorless
[Specific Gravity]

0.852
[Odor]

at 100.00 %. oily waxy fatty orris
[biological source]

plant (palm)
[Odor Type]

waxy
[Water Solubility ]

INSOLUBLE
[BRN ]

1780973
[Henry's Law Constant]

2.9×10-3 mol/(m3Pa) at 25℃, Krop and Velzen (1997)
[Cosmetics Ingredients Functions]

SKIN CONDITIONING
SKIN CONDITIONING - EMOLLIENT
PERFUMING
[InChI]

1S/C17H34O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17(18)19-2/h3-16H2,1-2H3
[InChIKey]

FLIACVVOZYBSBS-UHFFFAOYSA-N
[SMILES]

CCCCCCCCCCCCCCCC(=O)OC
[LogP]

7.38 at 36℃
[CAS DataBase Reference]

112-39-0(CAS DataBase Reference)
[NIST Chemistry Reference]

Hexadecanoic acid, methyl ester(112-39-0)
[EPA Substance Registry System]

112-39-0(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362
[Safety Statements ]

S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

1
[TSCA ]

Yes
[REACH Registrations]

Active
[HS Code ]

29157090
[Storage Class]

11 - Combustible Solids
[Hazardous Substances Data]

112-39-0(Hazardous Substances Data)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Palmitic acid-->Betulin
[Preparation Products]

4-Morpholineethanesulfonic acid-->Methyl 2(E)-Octadecenoate-->2-hydroxyethyl palmitate-->Glycidyl Palmitate-->Methyl alpha-eleostearate-->CIS-7,10,13,16,19-DOCOSAPENTAENOIC ACID METHYL ESTER
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Methyl hexadecanoate(112-39-0).msds
Hazard InformationBack Directory
[Description]

Saturated fatty acids are synthesized by both plants and animals from acetyl coenzyme A as a form of long-term energy storage. Palmitic acid is a common 16-carbon saturated fat that represents 10-20% of the normal human dietary fat intake, and approximately 25% of the total plasma fatty acids in plasma lipoproteins. Saturated free fatty acids induce the expression of cyclooxygenase-2. Palmitic acid methyl ester (MP) is a fatty acid ester whose concentration in cells is modulated by methanol. In studies with isolated Kupffer cells, MP inhibits phagocytosis and decreases cell viability. In cells treated with lipopolysaccharide, it also decreases secretion of interleukin-10, TNF-α, nitric oxide, and prostaglandin E2. This effect is thought to occur by the inhibition of NF-κB.
[Chemical Properties]

Clear colorless liquid or low melting solid
[Uses]

Methyl Palmitate is a fatty acid ester essential oil that naturally occurs in many plant species. Methyl Palmitate concentration in cells are known to be modulated by methanol. In experimental studies with isolated Kupffer cells, Methyl palmitate exhibited inhibitory activity towards phagocytosis and decreases cell viability.
[Application]

Methyl Palmitate is a fatty acid ester essential oil that naturally occurs in many plant species. Methyl Palmitate concentration in cells are known to be modulated by methanol. In experimental studies with isolated Kupffer cells, Methyl palmitate exhibited inhibitory activity towards phagocytosis and decreases cell viability.
[Definition]

ChEBI: A natural product found in Neolitsea daibuensis.
[Biological Functions]

Saturated fatty acids are synthesized by both plants and animals from acetyl coenzyme A as a form of long- term energy storage. Palmitic acid is a common 16-carbon saturated fat that represents 10-20% of the normal human dietary fat intake, and approximately 25% of the total plasma fatty acids in plasma lipoproteins. Saturated free fatty acids induce the expression of cyclooxygenase-2. Palmitic acid methyl ester (MP) is a fatty acid ester whose concentration in cells is modulated by methanol. In studies with isolated Kupffer cells, MP inhibits phagocytosis and decreases cell viability. In cells treated with lipopolysaccharide, it also decreases secretion of interleukin-10, TNF-α, nitric oxide, and prostaglandin E2. This effect is thought to occur by the inhibition of NF-κB.
[Synthesis Reference(s)]

Synthetic Communications, 16, p. 1423, 1986 DOI: 10.1080/00397918608056391
[General Description]

Methyl palmitate (PAME), a fatty acid ester of palmitic acid, is a muscurinic receptors antagonist. Methyl palmitate functions as a vasodilator and relaxes the arterioles in retina upon electrical depolarization. In the superior cervical ganglion, methyl palmitate modulates nicotinic receptor. Endogenous methyl palmitate modulates nicotinic receptor-mediated transmission in the superior cervical ganglion. PAME activates Kv7 channels and promotes perivascular adipose tissue.
[Flammability and Explosibility]

Nonflammable
[Biochem/physiol Actions]

Methyl palmitate has anti-inflammatory and anti-fibrotic effect. Methyl palmitate prevents bleomycin-induced lung inflammation and fibrosis in rats, by inhibiting NF-κB . Methyl palmitate also prevents CCl4-induced liver fibrosis linked to reduced TGF-β .
[Synthesis]

At present, there are two main methods to obtain methyl palmitate, one is to prepare fatty acid methyl ester mixture by transesterification reaction between palm oil and methanol under alkaline catalytic condition, which is used for biodiesel; the other o
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl palmitate(112-39-0)MS
Methyl palmitate(112-39-0)1HNMR
Methyl palmitate(112-39-0)13CNMR
Methyl palmitate(112-39-0)IR1
Methyl palmitate(112-39-0)IR2
Methyl palmitate(112-39-0)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Methyl palmitate, 95%(112-39-0)
[Alfa Aesar]

Methyl palmitate, 97%(112-39-0)
[Sigma Aldrich]

112-39-0(sigmaaldrich)
[TCI AMERICA]

Methyl Palmitate,>97.0%(GC)(112-39-0)
112-39-0 suppliers list
Company Name: SHANGHAI BANGCHENG CHEMICAL Co.,Ltd.  Gold
Telephone: 021-69106960 13701823997
Website: www.bangchengchem.com/
Company Name: Shanghai shengyue international trading co., ltd  Gold
Telephone: 021-66690837 13166269258
Website: www.zfshsy.com
Company Name: J & K SCIENTIFIC LTD.  
Telephone: 18210857532 18210857532
Website: https://www.jkchemical.com
Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
Telephone: 4006356688 18621169109
Website: www.x-labseek.com/
Company Name: future industrial shanghai co., ltd  
Telephone: 400-0066400 13621662912
Website: http://www.jonln.com
Company Name: Alfa Aesar  
Telephone: 400-6106006
Website: http://chemicals.thermofisher.cn
Company Name: TCI (Shanghai) Development Co., Ltd.  
Telephone: 021-67121386
Website: https://www.tcichemicals.com/CN/zh/
Company Name: Beijing HwrkChemical Technology Co., Ltd  
Telephone: 89508211 18501085097
Website: http://www.hwrkchemical.com
Company Name: Energy Chemical  
Telephone: 400-0056266
Website: www.energy-chemical.com
Company Name: JinYan Chemicals(ShangHai) Co.,Ltd.  
Telephone: 13817811078
Website: www.jingyan-chemical.com
Company Name: Nanjing Chemlin Chemical Co., Ltd  
Telephone: 025-83697070 13770331960
Website: www.echemlin.cn
Company Name: Shanghai Hanhong Scientific Co.,Ltd.  
Telephone: 021-54306202 13764082696
Website: https://www.hanhongsci.com
Company Name: Chemsky(shanghai)International Co.,Ltd.  
Telephone: 021-50135380
Website: www.shchemsky.com
Company Name: Beijing Isomersyn Technology CO;LTD  
Telephone: 010-82954736 13391601435
Website: www.chemicalbook.com/supplier/10680452/1.htm
Company Name: Shandong Xiya Chemical Co., Ltd  
Telephone: 13355009207 13355009207
Website: http://www.xiyashiji.com
Company Name: Syntechem Co.,Ltd  
Telephone:
Website: www.syntechem.com
Company Name: Sichuan Kulinan Technology Co., Ltd  
Telephone: 400-1166-196 18981987031
Website: http://www.hx-r.com/
Company Name: Tianjin heowns Biochemical Technology Co., Ltd.  
Telephone: 400 638 7771
Website: www.heowns.com
Tags:112-39-0 Related Product Information
57-10-3 1341-38-4 408-35-5 1492-30-4 112-67-4 74563-64-7 3155-48-4 2364-67-2 8015-86-9 111-06-8 2190-15-0 1716-07-0 8002-75-3 103833-72-3 1447824-23-8 68440-15-3 7501-44-2 1794941-80-2