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2718-37-8

2718-37-8 Structure

2718-37-8 Structure
IdentificationBack Directory
[Name]

2-HYDROXYTRICOSANOIC ACID
[CAS]

2718-37-8
[Synonyms]

2-HYDROXY C23:0 ACID
2-HYDROXYTRICOSANOIC ACID
JZWLIRVAYJRWLN-UHFFFAOYSA-N
Tricosanoic acid, 2-hydroxy-
Tricosanoic Acid Impurity 3
[Molecular Formula]

C23H46O3
[MDL Number]

MFCD00673438
[MOL File]

2718-37-8.mol
[Molecular Weight]

370.61
Chemical PropertiesBack Directory
[Boiling point ]

496.6±18.0 °C(Predicted)
[density ]

0.924±0.06 g/cm3(Predicted)
[solubility ]

Chloroform:Methanol (5:1): Soluble
[form ]

A solid
[pka]

3.86±0.21(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P321-P362+P364-P332+P313-P337+P313-P403+P233-P405-P501
Hazard InformationBack Directory
[Description]

2-hydroxy Tricosanoic acid is a hydroxylated fatty acid that has been found in the inner bark of E. globulus, the leaves of wild, kiyomi, and zweigeltrepe grape vines, C. elegans, and Pseudosuberites and S. massa sea sponges. [Matreya, LLC. Catalog No. 1713]
[Uses]

2-Hydroxytricosanoic Acid is a long chain saturated fatty acid found in sea cucumber and is known for exhibiting cytotoxic effects. Inhibits of cell proliferation.
[Definition]

ChEBI: 2-hydroxytricosanoic acid is a 2-hydroxy fatty acid that is tricosanoic acid substituted by a hydroxy group at position 2. It has a role as a marine metabolite and an animal metabolite. It is functionally related to a tricosanoic acid. It is a conjugate acid of a 2-hydroxytricosanoate.
[References]

[1] FREIRE C, SILVESTRE A, NETO C P, et al. Lipophilic Extractives of the Inner and Outer Barks of Eucalyptus globulus[C]//34 1. 2002: 0. DOI: 10.1515/hf.2002.059
[2] M KAWAGUCHI. Cerebrosides in grapevine leaves: distinct composition of sphingoid bases among the grapevine species having different tolerances to freezing temperature.[J]. Bioscience, Biotechnology, and Biochemistry, 2000, 64 6: 1271-1273. DOI: 10.1271/bbb.64.1271
[3] S GERDT. Isolation and structural analysis of three neutral glycosphingolipids from a mixed population of Caenorhabditis elegans (Nematoda:Rhabditida).[J]. Glycobiology, 1997, 7 2: 265-275. DOI: 10.1093/glycob/7.2.265
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