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Palmitic anhydride

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Palmitic anhydride Basic information

Product Name:
Palmitic anhydride
Synonyms:
  • hexadecanoicacid,anhydride
  • PALMITIC ANHYDRIDE
  • HEXADECANOIC ANHYDRIDE
  • PALMITIC ANHYDRIDE (C16:0) GRADE II
  • PALMITIC ANHYDRIDE (C16:0) GRADE I
  • Palmitic anhydride 99+%
  • Bishexadecanoic anhydride
  • Bispalmitic anhydride
CAS:
623-65-4
MF:
C32H62O3
MW:
494.83
EINECS:
210-805-0
Product Categories:
  • Anhydrides
  • Biochemicals and Reagents
  • Building Blocks
  • Carbonyl Compounds
  • Carboxylic Acid Anhydrides
  • Chemical Synthesis
  • Fatty Acids and conjugates
  • Fatty Acyls
  • Lipids
  • Organic Building Blocks
  • Saturated Fatty Acids and Derivatives
Mol File:
623-65-4.mol
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Palmitic anhydride Chemical Properties

Melting point:
61-64 °C (lit.)
Boiling point:
547.77°C (rough estimate)
Density 
0.8388
refractive index 
1.4364 (estimate)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
almost transparency in Toluene
form 
powder to crystal
color 
White to Almost white
BRN 
1807507
LogP
14.107 (est)
CAS DataBase Reference
623-65-4(CAS DataBase Reference)
EPA Substance Registry System
Palmitic acid anhydride (623-65-4)
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Safety Information

Hazard Codes 
C
Risk Statements 
34
Safety Statements 
26-36/37/39-45-25
RIDADR 
UN 3261 8/PG 2
WGK Germany 
3
10-21
HazardClass 
8
PackingGroup 
III
HS Code 
29159000

MSDS

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Palmitic anhydride Usage And Synthesis

Chemical Properties

white powder

Uses

Palmitic anhydride was used in the synthesis of water-soluble N-palmitoyl chitosan (PLCS) by coupling with swollen chitosan in dimethyl sulfoxide (DMSO). It was also used in the synthesis of N-acylphosphatidylserine.

General Description

Palmitic anhydride reacted with 20-methyl spirolide G to form a derivative with a retention time and spectrum identical with the metabolite, 17-O-palmitoyl-20-methyl spirolide G.

Purification Methods

It is moisture sensitive and hydrolyses in water. Purify it by refluxing with acetic anhydride for 1hour, evaporating and freeing the residue of acetic acid and anhydride by drying the residue at high vacuum and recrystallising from pet ether at low temperature. [Beilstein 2 IV 1181.]

Palmitic anhydrideSupplier

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