2433-95-6

Basic information

• Product Name: DL-2-HYDROXYTETRACOSANOIC ACID METHYL ESTER
• Synonyms: DL-2-HYDROXYTETRACOSANOIC ACID METHYL ESTER;METHYL 2-HYDROXYTETRACOSANOATE;2-HYDROXY C24:0 METHYL ESTER;2-hydroxytetracosanoic acid*methyl ester;2-hydroxy Lignoceric Acid methyl ester
• CAS NO: 2433-95-6
• Molecular Formula: C₂₅H₅₀O₃
• Molecular Weight: 398.66
• Mol File: 2433-95-6.mol
• Article Data: 5

Chemical Properties

• Melting Point: 68-68.5 °C
• Boiling Point: 423.9°C at 760 mmHg
• Flash Point: 198°C
• Appearance: /
• Density: 0.9g/cm³
• Vapor Pressure: 5.82E-09mmHg at 25°C
• Refractive Index: 1.459
• Storage Temp.: 2-8°C
• PKA: 13.03±0.20(Predicted)
• CAS DataBase Reference: DL-2-HYDROXYTETRACOSANOIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: DL-2-HYDROXYTETRACOSANOIC ACID METHYL ESTER(2433-95-6)
• EPA Substance Registry System: DL-2-HYDROXYTETRACOSANOIC ACID METHYL ESTER(2433-95-6)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 2433-95-6(Hazardous Substances Data)

Usage

Description

DL-2-HYDROXYTETRACOSANOIC ACID METHYL ESTER, also known as 2-hydroxy Lignoceric acid methyl ester, is a hydroxylated fatty acid methyl ester that has been identified in various natural sources such as ripe and unripe strawberry homogenates, Pseudosuberites and S. massa sea sponges, sediment samples from the Harney River and Lake Kivu, and the aerial parts of E. helioscopia.
Usage:
There is no specific information provided about the uses of DL-2-HYDROXYTETRACOSANOIC ACID METHYL ESTER in the given materials. However, based on its classification as a hydroxylated fatty acid methyl ester, it can be inferred that it may have potential applications in the following industries:
Used in Pharmaceutical Industry:
DL-2-HYDROXYTETRACOSANOIC ACID METHYL ESTER could be used as a pharmaceutical compound for its potential therapeutic properties, such as anti-inflammatory, antioxidant, or antimicrobial activities, which are common among hydroxylated fatty acid derivatives.
Used in Cosmetic Industry:
In the cosmetic industry, DL-2-HYDROXYTETRACOSANOIC ACID METHYL ESTER might be utilized as an ingredient in skincare or hair care products due to its potential moisturizing, emollient, or conditioning properties, which are often desired in cosmetic formulations.
Used in Food Industry:
As a component of natural extracts, DL-2-HYDROXYTETRACOSANOIC ACID METHYL ESTER could be used in the food industry as a additives for enhancing flavor, texture, or shelf-life of certain products.
Please note that these potential applications are speculative and would require further research and validation to confirm their suitability and efficacy.

InChI:InChI=1/C25H50O3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24(26)25(27)28-2/h24,26H,3-23H2,1-2H3

Upstream product

• 67-56-1 methanol 
• 148347-44-8 (2S,3S,4R,2''R)-1-O-α-D-galactopyranosyl-2-N-(2''-hydroxy-tetracosanoyl)hexadecane-3,4-diol 
• 148289-27-4 agelasphin-9a 
• 154801-30-6 (2S,3S,4R)-2-<(2R)-2-hydroxytetracosanoylamino>-1,3,4-octadecanetriol 
• 193412-78-1 1-O-β-D-glucopyranosyl-(2S,3S,4R,9Z)-2-[(2R)-2-hydroxytetracosanoylamino]-1,3,4-octadecanetriol 
• 152139-44-1 agelasphin-11 
• 148766-51-2 (2S,3S,4R)-1-O-(α-D-galctopyranosyl)-16-methyl-2--1,3,4-heptadecanetriol 

Downstream Products

• 112146-60-8 (2R)-2-tert-butyldiphenylsilyloxytetracosanoic acid 
• 64655-47-6 (2S,3R,4E)-N-(2'R)-2'-hydroxytetracosanoylsphingenine 
• 112146-62-0 (2S,3R,4E)-N-(2'R)-2'-tert-butyldiphenylsilyloxytetracosanoyl-1,3-di-O-(1-ethoxyethyl)-sphingenine 
• 112146-63-1 (2S,3R,4E)-N-(2'R)-2'-tert-butyldiphenylsilyloxytetracosanoylsphingenine 
• 112146-59-5 methyl (2R)-2-tert-butyldiphenylsilyloxytetracosanoate 
• 112146-61-9 methyl (2R)-2-(-)-α-methoxy-α-trifluoromethylphenylacetyloxytetracosanoate 

Relevant articles and documents

Ceramide and cerebroside from the stem bark of Ficus mucuso (Moraceae)

Two new sphingolipids mucusamide (1) and mucusoside (2) have been isolated from methanol soluble part of the stem bark of Ficus mucuso WELW., together with fifteen known secondary metabolites including cellobiosylsterol (3), β-sitosterol (4), stigmasterol (5), β-sitosterol 3-O-β-D- glucopyranoside (6), lupeol acetate (7), ursolic acid (8), procatechuic acid (9), 2-methyl-5,7-dihydroxychromone 8-C-β-D-glucoside (10), apigenin (11), (-)-epicatechin (12), (+)-catechin (13), N-benzoyl-L-phenylalanilol (14), α-acetylamino-phenylpropyl α-benzoylaminophenylpropionate (15), asperphenamate (16) and bejaminamide (17). Structures of compounds 1 and 2 were elucidated by spectroscopic analysis and chemical methods.

Preliminary biological assay on cerebroside mixture from Euphorbia nicaeensis All. Isolation and structure determination of five glucocerebrosides

Preliminary studies of in vitro cytostatic activity on less polar fraction of the MeOH extract of the plant Euphorbia nicaeensis All., carried out on KB cells, have evinced a relatively low ability of extract to inhibit cell growth. Successive, five glucocerebrosides were isolated from the cerebroside molecular species obtained from this extract using normal and reversed phase column 'flash-chromatography'. The structures of these cerebrosides were determined on the basis of chemical and spectroscopic evidences. Mass spectrometry of dimethyl disulfide derivatives was useful for the determination of the double-bond positions in the long-chain bases.

Agelasphins, novel antitumor and immunostimulatory cerebrosides from the marine sponge Agelas mauritianus

New glycosphingolipids, named agelasphins (1-8), have been isolated by antitumor and immunostimulatory bioassay-guided purification from an extract of a marine sponge, Agelas mauritianus. Strongly active agents in agelasphins had characteristic α-galactosylceramide structures, the isolation of which from natural products has not previously been reported. The absolute configurations of agelasphins were elucidated by the total synthesis.