palmitic anhydride

hexadecanoic acid, anhydride

CAS: 623-65-4 C32 H62 O3 MW: 494.84374000

Identification

Namepalmitic anhydride
CAS Number623-65-4
EINECS210-805-0
FDA UNII33JHB8GS96
Molecular FormulaC32 H62 O3
Molecular Weight494.84374000
MDL NumberMFCD00008992
Nikkaji NumberJ24.134B
Beilstein1807507

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Melting Point 64.00 °C. @ 760.00 mm Hg
Boiling Point 488.65 °C. @ 760.00 mm Hg (est)
Flash Point 429.00 °F. TCC ( 220.60 °C. ) (est)
logP (o/w) 14.107 (est)
Soluble in water, 4.344e-009 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for palmitic anhydride usage levels up tonot for fragrance use.
Recommendation for palmitic anhydride flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

prunus tomentosa

Synonyms

hexadecanoic acid, anhydride hexadecanoic anhydride hexadecanoyl hexadecanoate palmitic acid anhydride palmiticanhydride PubMed: Assessment of acylation routes and structural characterisation by liquid chromatography/tandem mass spectrometry of semi-synthetic acyl ester analogues of lipophilic marine toxins. PubMed: Discovery of fatty acid ester metabolites of spirolide toxins in mussels from Norway using liquid chromatography/tandem mass spectrometry. PubMed: Novel polymer micelles prepared from chitosan grafted hydrophobic palmitoyl groups for drug delivery. PubMed: Biologically active ether lipids. Biotransformation of rac-1(3)-O-alkylglycerols in cell suspension cultures of rape and semisynthesis of 1-O-alkyl-2-palmitoyl-sn-glycero-3-phospho-(N-palmitoyl)ethanolamines, potent antitumor agents. PubMed: Purification and characterization of an N-acylphosphatidylserine from Rhodopseudomonas sphaeroides.