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PALMITOLEIC ACID

Basic information Safety Supplier Related

PALMITOLEIC ACID Basic information

Product Name:
PALMITOLEIC ACID
Synonyms:
  • CIS-9-HEXADECENOIC ACID
  • DELTA 9 CIS HEXADECENOIC ACID
  • C16:1 (CIS-9) ACID
  • 9-HEXADECENOIC ACID
  • RARECHEM AL BE 0686
  • PALMITOLEIC ACID
  • cis-Hexadec-9-enoic acid
  • cis-Palmitoleic acid
CAS:
373-49-9
MF:
C16H30O2
MW:
254.41
EINECS:
206-765-9
Product Categories:
  • Biochemistry
  • Higher Fatty Acids & Higher Alcohols
  • Unsaturated Higher Fatty Acids
Mol File:
373-49-9.mol
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PALMITOLEIC ACID Chemical Properties

Melting point:
0.5 °C (lit.)
Boiling point:
162 °C/0.6 mmHg (lit.)
Density 
0.895 g/mL at 20 °C (lit.)
refractive index 
1.457-1.459
Flash point:
62 °C
storage temp. 
-20°C
solubility 
Chloroform, Methanol (Slightly)
pka
4.78±0.10(Predicted)
form 
Liquid
color 
Clear
BRN 
1725389
InChIKey
SECPZKHBENQXJG-FPLPWBNLSA-N
LogP
6.402 (est)
CAS DataBase Reference
373-49-9(CAS DataBase Reference)
EPA Substance Registry System
9-Hexadecenoic acid, (9Z)- (373-49-9)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
37/39-26-36
RIDADR 
NA 1993 / PGIII
WGK Germany 
3
HS Code 
29161995

MSDS

  • Language:English Provider:ACROS
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PALMITOLEIC ACID Usage And Synthesis

Description

Palmitoleic acid, or (Z)-9-hexadecenoic acid, is an omega - 7 mono unsaturated fatty acid with the formula CH3(CH2)5CH=CH(CH2)7COOH that is a common constituent of the glycerides of human adipose tissue. It is present in all tissues, but generally found in higher concentrations in the liver. It is biosynthesized from palmitic acid by the action of the enzyme delta-9 desaturase. A beneficial fatty acid, it has been shown to increase insulin sensitivity by suppressing inflammation, as well as inhibit the destruction of insulin-secreting pancreatic beta cells.

Chemical Properties

clear liquid

Chemical Properties

PALMITOLEIC ACID, Also called cis-9-hexa decanoic acid, formula CH3(CH2)5CH:CH(CH2)7COOH. This is an unsaturated fatty acid found in nearly every fat, especially in marine oils (15–20%). At room temperature, it is a colorless liquid. Insoluble in water; soluble in alcohol and ether. Insoluble in water; soluble in alcohol and ether. Combustible.

Occurrence

Palmitoleic acid can be abbreviated as 16:1Δ9. Dietary sources of palmitoleic acid include a variety of animal oils, vegetable oils, and marine oils. Macadamia oil (Macadamia integrifolia) and sea buckthorn oil (Hippophae rhamnoides) are botanical sources with high concentrations, containing 17 % and 40 % of palmitoleic acid, respectively.

Uses

Palmitoleic acid is used in organic synthesis, and as a standard in chromatographic analysis.

Uses

Palmitoleic Acid is a polyunsaturated fatty acid which contributes to reduced protein oxidation in mammals.

Definition

ChEBI: A hexadecenoic acid with a cis-double bond at position C-9.

General Description

Palmitoleic acid is a monounsaturated fatty acid found in macadamia oil and also in blood plasma. In the human body it is produced via endogenous fat synthesis.

Biochem/physiol Actions

Palmitoleic acid is a 16-carbon, omega-7, monounsaturated fatty acid that is enriched in the triglycerides of human adipose tissue and in liver.

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