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	Myristic acid
	Myristic acid

Myristic acid

Price USD1.00
Packge 1kg
  • Min. Order:1kg
  • Supply Ability:100KG
  • Time:2019-07-06

Product Details

  • Product Name Myristic acid
  • CAS No. 544-63-8
  • EINECS No.208-875-2
  • MFC14H28O2
  • MW228.37
  • InChIKeyTUNFSRHWOTWDNC-UHFFFAOYSA-N
  • AppearanceFlakes, Powder, Chunks or Crystalline MassWhite
  • Melting point 52-54 °C(lit.)
  • storage temp. room temp
  • Boiling point 250 °C100 mm Hg(lit.)
  • density 0.862
  • Water Solubility <0.1 g/100 mL at 18 ºC

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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: Miscellaneous Natural Products;Alkylcarboxylic Acids;Biochemistry;Color Former & Related Compounds;Functional Materials;Higher Fatty Acids & Higher Alcohols;Monofunctional & alpha,omega-Bifunctional Alkanes;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
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 Reference 544-63-8(CAS DataBase Reference)
NIST Chemistry Reference Tetradecanoic acid(544-63-8)
EPA Substance Registry System Tetradecanoic 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 Data 544-63-8(Hazardous Substances Data)
Toxicity LD50 i.v. in mice: 432.6 mg/kg (Or, Wretlind)
MSDS Information
Provider Language
1-Tridecanecarboxylic acid English
SigmaAldrich English
ACROS English
ALFA English
 
Myristic acid Usage And Synthesis
Chemical properties It 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.
Preparation To 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.
Toxicity Natural fatty acids, non-toxic
Can be safely used for food (FDA, § 172.860; 2000).
LD50:43 mg/kg (mouse, transdermal).
Use limit FEMA (mg/kg): soft drinks 5.3, cold drinks 2.6~10, candy 4.1, baked goods 5.3, pudding class 0.10.
Chemical Properties white solid
Uses Myristic Acid is a common saturated fatty acid found in nutmeg, palm kernel oil, coconut oil and butter fat.
Uses myristic 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.
Definition ChEBI: A straight-chain, fourteen-carbon, long-chain saturated fatty acid mostly found in milk fat.
Uses Myristic 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 Description Oily white crystalline solid.
Air & Water Reactions Insoluble in water.
Reactivity Profile Myristic 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 Hazard Myristic acid is probably combustible.
Safety Profile Poison by intravenous route. Mutation data reported. An eye and human skin irritant. When heated to decomposition it emits acrid smoke and irritating fumes.
Purification Methods Purify 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.]
 

Company Profile Introduction

Henan CoreyChem Co., Ltd, based on the original Zhengzhou Cote Chemical Research Institute, be brave in absorbing highly educated talents & overseas returnees; actively responded to Zhengzhou City High-tech Zone Government’s Special Care Policy, reorganized and founded in National University of Science and Technology Park, which is a high-tech, stock enterprise of high-end chemical Custom synthesis;The park was created by the People's Government of Henan Province, and proved by Ministry of Education and the National Science & Technology, taking the construction mode of "many college a park, and common development", mainly depends on Zhengzhou University and Henan University’s scientific research and talent advantage to set up Universities, scientific research institute and enterprise scientific research achievements transformation platform, to make high-tech enterprises incubate,  is the new high-tech talent gathering base, high and new technology industry enterprise radiation base, colleges and universities technological innovation base.
 
Henan Coreychem Co., Ltd, facing global High-tech pharmaceutical raw materials, high complex new type intermediates, fine chemicals custom synthesis, scale-up production and Rare chemicals trade. Corey have well-equipped machine, strong technical force and considerate marketing team service. We also have rich experience advantage in basic research, small scale process development, scale-up, industrial technology development & production and cost control.
 

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  • Since:2014-12-17
  • Address: No.967,15th Floor,Unit 7, Building 1, No.70 of DianChang Road, High-tech Development Zone, Zhengzho
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