Palmitoyl chloride

Palmitoyl chloride Basic information
Product Name:Palmitoyl chloride
Synonyms:PalMitoyl chloride, 98% 100ML;Palmitoyl chloride,98%;Palmitoyl chloride,92%,tech.;PALMITOYL CHLORIDE FOR SYNTHESIS;Palm acetyl chlorine(14 acetyl chlorine);hexadecanoicacid,chloride;CETYLOYL CHLORIDE;N-HEXADECANOYL CHLORIDE
CAS:112-67-4
MF:C16H31ClO
MW:274.87
EINECS:203-996-7
Product Categories:Acid Halides;Bioactive Small Molecules;Building Blocks;Carbonyl Compounds;Cell Biology;Chemical Synthesis;Organic Building Blocks;P;ACID CHLORIDES
Mol File:112-67-4.mol
Palmitoyl chloride Structure
Palmitoyl chloride Chemical Properties
Melting point 11-13 °C (lit.)
Boiling point 88-90 °C/0.2 mmHg (lit.)
density 0.906 g/mL at 25 °C (lit.)
refractive index n20/D 1.452(lit.)
Fp >230 °F
storage temp. Store below +30°C.
solubility Chloroform (Sparingly), Ethyl Acetate (Slightly)
form Liquid
Specific Gravity0.905
color Clear
Water Solubility Decomposition
Sensitive Moisture Sensitive
BRN 972409
Stability:Moisture Sensitive
CAS DataBase Reference112-67-4(CAS DataBase Reference)
NIST Chemistry ReferencePalmitoyl chloride(112-67-4)
EPA Substance Registry SystemHexadecanoyl chloride (112-67-4)
Safety Information
Hazard Codes C
Risk Statements 14-34-29
Safety Statements 26-36/37/39-43-45-8
RIDADR UN 3265 8/PG 2
WGK Germany 1
9-21
TSCA Yes
HS Code 2915 90 70
HazardClass 8
PackingGroup II
Hazardous Substances Data112-67-4(Hazardous Substances Data)
ToxicityLD50 orally in Rabbit: > 2000 mg/kg
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
Palmitoyl chloride Usage And Synthesis
Chemical Propertiesclear liquid
UsesPalmitoyl chloride is a compound which has been used as a polymeric carrier for plasmid DNA delivery to 293T cells.
UsesPalmitoyl Chloride was used as a polymeric carriers for plasmid DNA (pDNA) delivery to 293T cells.
Synthesis Reference(s)The Journal of Organic Chemistry, 54, p. 6101, 1989 DOI: 10.1021/jo00287a023
General DescriptionA clear colorless to light yellow liquid with a pungent odor. Freezing point 11-12°C. Irritates skin, eyes, and mucous membranes. May be toxic by ingestion, inhalation and skin absorption.
Air & Water ReactionsDecomposes rather slowly in water to form hydrochloric acid and palmitic acid, a fatty acid that is not soluble in water.
Reactivity ProfileHEXADECANOYL CHLORIDE is incompatible with bases (including amines), with strong oxidizing agents, and with alcohols. May react vigorously or explosively if mixed with diisopropyl ether or other ethers in the presence of trace amounts of metal salts [J. Haz. Mat., 1981, 4, 291].
Health HazardTOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.
Fire HazardNon-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Some are oxidizers and may ignite combustibles (wood, paper, oil, clothing, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated.
Flammability and ExplosibilityNotclassified
Ethylhexyl Palmitate PALMITIC ACID VINYL ESTER PALMITELAIDIC ACID Palmitic acid ethyl ester Isopalmitic chloride BEHENOYL CHLORIDE FV301400 POLYVINYLIDENEFLUORIDE Propionyl chloride TRICOSANOYL CHLORIDE Pivaloyl chloride LIGNOCEROYL CHLORIDE NONADECANOYL CHLORIDE MARGAROYL CHLORIDE Protein hydrolyzates, wheat, reaction products with palmitoyl chloride 2-METHYLOCTADECANOYL CHLORIDE ARACHIDOYL CHLORIDE 2-​[[(2-​ethylphenyl)​(2-​hydroxyethyl)​amino]​methyl]​-​3,​3-​difluoro-Propanenitrile HENEICOSANOYL CHLORIDE

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