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Palmitic acid

Palmitic acid Suppliers list
Company Name: Hebei Guanlang Biotechnology Co., Ltd.
Tel: +86-0311-66562153 whatsapp +8615203118427
Email: sales@crovellbio.com
Products Intro: Product Name:Palmitic acid
CAS:57-10-3
Purity:99% Package:25kg
Company Name: Capot Chemical Co.,Ltd.
Tel: +86 (0)571-855 867 18
Email: sales@capotchem.com
Products Intro: Product Name:Palmitic acid
CAS:57-10-3
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
Company Name: Mainchem Co., Ltd.
Tel: +86-0592-6210733
Email: sales@mainchem.com
Products Intro: Product Name:Palmitic acid
CAS:57-10-3
Company Name: Chengdu Biopurify Phytochemicals Ltd.
Tel: 18080483897
Email: maggie@biopurify.com
Products Intro: Product Name:Palmitic acid
CAS:57-10-3
Purity:98% HPLC Package:20mg;100mg;500mg;1g Remarks:BP3411
Company Name: career henan chemical co
Tel: +86-371-86658258
Email: sales@coreychem.com
Products Intro: Product Name:Palmitic acid
CAS: 57-10-3
Purity:99% Package:1kg;1USD

Lastest Price from Palmitic acid manufacturers

  • Palmitic acid
  • US $1.00 / kg
  • 2018-12-18
  • CAS: 57-10-3
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 100KG
Palmitic acid Chemical Properties
Melting point 61-62.5 °C(lit.)
Boiling point 351.5 °C
density 0.852 g/mL at 25 °C(lit.)
vapor pressure 10 mm Hg ( 210 °C)
refractive index 1.4273
FEMA 2832 | PALMITIC ACID
Fp >230 °F
storage temp. +15C to +30C
solubility chloroform: 0.5 M, clear, colorless
form Flakes
color White or almost white
Water Solubility insoluble
Merck 14,6996
BRN 607489
Stability:Stable. Combustible. Incompatible with bases, oxidizing agents, reducing agents.
CAS DataBase Reference57-10-3(CAS DataBase Reference)
NIST Chemistry ReferenceHexadecanoic acid(57-10-3)
EPA Substance Registry SystemHexadecanoic acid(57-10-3)
Safety Information
Hazard Codes Xi
Risk Statements 36-36/38-36/37/38
Safety Statements 26-37/39-36
WGK Germany -
RTECS RT4550000
TSCA Yes
HS Code 29157015
Hazardous Substances Data57-10-3(Hazardous Substances Data)
ToxicityLD50 i.v. in mice: 57±3.4 mg/kg (Or, Wretlind)
MSDS Information
ProviderLanguage
Hexadecanoic acid English
SigmaAldrich English
ACROS English
ALFA English
Palmitic acid Usage And Synthesis
DescriptionPalmitic acid is a kind of common saturated fatty acid of a 16-carbon backbone, which is contained in fats and waxes.  It naturally exists in palm oil and palm kernel oil, and can also be found in butter, cheese, milk, meat, cocoa butter, soybean oil and sunflower oil. It can be produced by many kinds of plants and organisms.  It can be used for the production of soap, cosmetics, and industrial mold release agents. It is also a food processing aid. It can also be used to produce cetyl alocohol which is useful in the production of detergents and cosmetics. Recently, it has been also used for the manufacture of a long-acting antipsychotic medication, paliperidone palmitate.
Referenceshttps://pubchem.ncbi.nlm.nih.gov/compound/palmitic_acid#section=Top
https://en.wikipedia.org/wiki/Palmitic_acid
Chemical Propertieswhite chips, crystals or powder
UsesPalmitic Acid is a common fatty acid found in plants and animals. The body converts excess carbohydrates into Palmitic Acid, thus Palmitic Acid is the first fatty acid produced during fatty acid synt hesis as well as a precursor for longer fatty acids.
Usespalmitic acid is one of the skin’s major fatty acids produced by the sebaceous glands. In cosmetic preparations, it is used as a formula texturizer. This acid is naturally occurring in allspice, anise, calamus oil, cascarilla bark, celery seed, coffee, tea, and many animal fats and plant oils. It is obtained from palm oil, Japan wax, or Chinese vegetable tallow.
UsesPalmitic Acid is a fatty acid which is a mixture of solid organic acids from fats consisting principally of palmitic acid with varying amounts of stearic acid. it functions as a lubricant, binder, and defoaming agent.
DefinitionChEBI: A straight-chain, sixteen-carbon, saturated long-chain fatty acid.
Safety ProfileA poison by intravenous route. A human skin irritant. Questionable carcinogen with experimental neoplastigenic data. When heated to decomposition it emits acrid smoke and irritating fumes
Purification MethodsPurify palmitic acid by slow (overnight) recrystallisation from hexane. Some samples are also crystallised from acetone, EtOH or EtOAc. The crystals are kept in air to lose solvent, or are pumped dry of solvent on a vacuum line. [Iwahashi et al. J Chem Soc, Faraday Trans 1 81 973 1985, pK: White J Am Chem Soc 72 1858 1950, Beilstein 2 IV 1157.]
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