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Myristic acid

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Company Name: Hebei Guanlang Biotechnology Co., Ltd.
Tel: +86-0311-66562153 whatsapp +8615203118427
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Products Intro: Product Name:Myristic acid
CAS:544-63-8
Purity:99% Package:25kg
Company Name: Henan DaKen Chemical CO.,LTD.
Tel: +86-371-55531817
Email: info@dakenchem.com
Products Intro: Product Name:Myristic acid
CAS:544-63-8
Purity:99% Package:100g,500g,1KG,10KG,100KG
Company Name: Henan Tianfu Chemical Co.,Ltd.
Tel: 0371-55170693
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Products Intro: CAS:544-63-8
Purity:99% Package:500G;1KG;5KG;25KG
Company Name: Mainchem Co., Ltd.
Tel: +86-0592-6210733
Email: sales@mainchem.com
Products Intro: Product Name:Myristic acid
CAS:544-63-8
Company Name: Hefei TNJ Chemical Industry Co.,Ltd.
Tel: 86-0551-65418684 18949823763
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Products Intro: Product Name:Myristic acid
CAS:544-63-8
Purity:99.9% Package:1KG;5USD

Lastest Price from Myristic acid manufacturers

  • Myristic acid
  • US $1.00 / kg
  • 2018-12-18
  • CAS: 544-63-8
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 100KG
Myristic acid Basic information
Chemical properties Application Preparation Toxicity Use limit
Product Name:Myristic acid
Synonyms:acidemyristique;acidetetradecanoique;Crodacid;EdenorC14;Emery 654;Emery 655;emery655;Hydrofol acid 1495
CAS:544-63-8
MF:C14H28O2
MW:228.37
EINECS:208-875-2
Product Categories:Alkylcarboxylic Acids;Biochemistry;Color Former & Related Compounds;Functional Materials;Higher Fatty Acids & Higher Alcohols;Monofunctional & alpha,omega-Bifunctional Alkanes;Miscellaneous Natural Products;Monofunctional Alkanes;Saturated Higher Fatty Acids;Sensitizer
Mol File:544-63-8.mol
Myristic acid Structure
Myristic acid Chemical Properties
Melting point 52-54 °C(lit.)
Boiling point 250 °C100 mm Hg(lit.)
density 0.862
vapor pressure <0.01 hPa (20 °C)
FEMA 2764 | MYRISTIC ACID
refractive index nD60 1.4305; nD70 1.4273
Fp >230 °F
storage temp. −20°C
solubility 1.07mg/l
form Flakes, Powder, Chunks or Crystalline Mass
color White
Water Solubility <0.1 g/100 mL at 18 ºC
Merck 14,6333
BRN 508624
Stability:Stable. Incompatible with strong oxidizing agents, bases.
CAS DataBase Reference544-63-8(CAS DataBase Reference)
NIST Chemistry ReferenceTetradecanoic acid(544-63-8)
EPA Substance Registry SystemTetradecanoic acid(544-63-8)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38-38
Safety Statements 24/25
WGK Germany -
RTECS QH4375000
TSCA Yes
HS Code 29159080
Hazardous Substances Data544-63-8(Hazardous Substances Data)
ToxicityLD50 i.v. in mice: 432.6 mg/kg (Or, Wretlind)
MSDS Information
ProviderLanguage
1-Tridecanecarboxylic acid English
SigmaAldrich English
ACROS English
ALFA English
Myristic acid Usage And Synthesis
Chemical propertiesIt appears as white to yellowish white solid, sometimes appearing as shiny crystalline solid, or white to yellowish white powder. It has a relative density of 0.8739 (80 ℃), melting point of 54.5 ℃ and the boiling point of 326.2 ℃. Its refractive index (nD60) is 1.4310. It is not soluble in water but soluble in ethanol, ether and chloroform.
Myristin contains about 70% to 80% while other kinds of coconut oil, palm kernel oil also contain it.
Application
  • It can be used as a chemical agent, also for the synthesis of spices and organic matter
  • It can be used in the manufacture of emulsifiers, waterproofing agents, curing agents, PVC heat stabilizers and plasticizers, and also used as the raw materials of spices and pharmaceutical.
  • It is mainly used as raw materials for the production of surfactants for the production of sorbitan fatty acid esters, glycerol fatty acid esters, ethylene glycol or propylene glycol fatty acid esters. It can also be used for the production of isopropyl myristate and so on. It can also be used for defoamers and flavoring agent. According to the provision of China GB2760-89, it can be used to prepare a variety of food spices.
PreparationTo prepare the myristic acid, the methyl ester of the mixed fatty acids or mixed fatty acid methyl ester obtained from the coconut oil or palm kernel oil is subject to vacuum fractionation, obtaining myristic acid. For laboratory preparation, glycerol tris (tetradecanoate) is subject to saponification with 10% sodium hydroxide solution, further being acidified with hydrochloric acid to obtain the free myristic acid. It can also be made from tetradecanol.
ToxicityNatural fatty acids, non-toxic
Can be safely used for food (FDA, § 172.860; 2000).
LD50:43 mg/kg (mouse, transdermal).
Use limitFEMA (mg/kg): soft drinks 5.3, cold drinks 2.6~10, candy 4.1, baked goods 5.3, pudding class 0.10.
Chemical Propertieswhite solid
UsesMyristic Acid is a common saturated fatty acid found in nutmeg, palm kernel oil, coconut oil and butter fat.
Usesmyristic acid is a surfactant and cleansing agent. When combined with potassium, myristic acid soap provides very good, abundant lather. This is a solid organic acid naturally occurring in butter acids such as nutmeg, oil of lovage, coconut oil, mace oil, and most animal and vegetable fats. Although some sources cite it as having no irritation potential, they do indicate comedogenicity potential.
UsesMyristic Acid is a fatty acid obtained from coconut oil and other fats. it has poor water solubility but is soluble in alcohol, chloro- form, and ether. it is used as a lubricant, binder, and defoaming agent.
DefinitionChEBI: A straight-chain, fourteen-carbon, long-chain saturated fatty acid mostly found in milk fat.
UsesMyristic acid is a 14-carbon saturated (14:0) fatty acid. In vivo, it is commonly added covalently to the N-terminus of proteins in a co-translational process termed N-myristoylation. In addition, there are examples where N-myristoylation occurs post-translationally, when a hidden myristoylation pattern is exposed.
General DescriptionOily white crystalline solid.
Air & Water ReactionsInsoluble in water.
Reactivity ProfileMyristic acid is a carboxylic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in Myristic acid to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions.
Fire HazardMyristic acid is probably combustible.
Safety ProfilePoison by intravenous route. Mutation data reported. An eye and human skin irritant. When heated to decomposition it emits acrid smoke and irritating fumes.
Purification MethodsPurify the acid via the methyl ester (b 153-154o/10mm, n25 1.4350), as for capric acid. [Trachtman & Miller J Am Chem Soc 84 4828 1962.] Also purify it by zone melting. It crystallises from pet ether, and is dried in a vacuum desiccator containing shredded wax. [Beilstein 2 IV 1126.]
Tag:Myristic acid(544-63-8) Related Product Information
Palmitic acid FATTY ACID KIT HENEICOSANOIC ACID 16-HYDROXYHEXADECANOIC ACID Docosanoic acid PENTADECANOIC ACID HEXADECANOIC ACID-1-13C HEXADECANEDIOIC ACID OCTADECANOIC ACID-1-13C Ethyl myristate Myristic acid methyl,Tetradecanoic acid methyl Ascoric Acid ACETIC ACID Myristic acid LIGNOCERIC ACID Hyaluronic acid MYRISTYL MYRISTATE Citric acid