aleuritic acid

hexadecanoic acid, 9,10,16-trihydroxy-

CAS: 6949-98-0 C16 H32 O5 MW: 304.42704000

Identification

Namealeuritic acid
IUPAC9,10,16-trihydroxyhexadecanoic acid
CAS Number6949-98-0
FDA UNIISearch
Molecular FormulaC16 H32 O5
Molecular Weight304.42704000
MDL NumberMFCD00021797
Nikkaji NumberJ21.879K

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Soluble in water, 110.6 mg/L @ 25 °C (est)

Cosmetic Information

CosIngcosmetic data
Cosmetic Usesskin conditioning

No sensory data available

Safety Information

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

Categorycosmetic ingredient for skin conditioning
Recommendation for aleuritic acid usage levels up tonot for fragrance use.
Recommendation for aleuritic acid flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

found in nature

Synonyms

aleuritolic acid hexadecanoic acid, 9,10,16-trihydroxy- 9,10,16- trihydroxyhexadecanoic acid PubMed: [Chemical Constituents from Macaranga denticulata Root]. PubMed: Antibacterial effects of Alchornea cordifolia (Schumach. and Thonn.) Müll. Arg extracts and compounds on gastrointestinal, skin, respiratory and urinary tract pathogens. PubMed: Antinociceptive and anti-inflammatory activities of Schefflera octophylla extracts. PubMed: Pectin-lipid self-assembly: influence on the formation of polyhydroxy fatty acids nanoparticles. PubMed: Anti-HIV and NO production inhibition activities of epi-aleuritolic acid derivatives. PubMed: Antioxidant capacity, antimicrobial activity and triterpenes isolated from Jatropha isabellei Müll Arg. PubMed: New triterpenoids from the stem bark of Hypodaphnis zenkeri. PubMed: Anti-inflammatory diterpene from Thyrsanthera suborbicularis. PubMed: Triterpenes from Garcia parviflora. Cytotoxic evaluation of natural and semisynthetic friedelanes. PubMed: Croton cajucara crude extract and isolated terpenes: activity on Trypanosoma cruzi. PubMed: Aleuritic (9,10,16-trihydroxypalmitic) acid self-assembly on mica. PubMed: [Study on the chemical constituents of liposoluble steroidal and triterpenoid compounds from the stem and bark of Macaranga hemsleyana]. PubMed: Antibacterial activities and cytotoxicity of terpenoids isolated from Spirostachys africana. PubMed: Seco-terpenoids and other constituents from Elateriospermum tapos. PubMed: Anti-inflammatory compounds from leaves and root bark of Alchornea cordifolia (Schumach. & Thonn.) Müll. Arg. PubMed: Chemical constituents from the roots of Homonoia riparia. PubMed: Gastroprotective effect and cytotoxicity of terpenes from the Paraguayan crude drug "yagua rova" (Jatropha isabelli). PubMed: Antifilarial activity in vitro of polycarpol and 3-O-acetyl aleuritolic acid from cameroonian medicinal plants against Onchocerca gutturosa. PubMed: [Study on chemical constituents from stem of Mallotus apelta]. PubMed: An effective use of benzoic anhydride and its derivatives for the synthesis of carboxylic esters and lactones: a powerful and convenient mixed anhydride method promoted by basic catalysts. PubMed: Rearranged jatrophane-type diterpenes from euphorbia species. Evaluation of their effects on the reversal of multidrug resistance. PubMed: New reagents for the introduction of reactive functional groups into chemically synthesized DNA probes. PubMed: Ethnopharmacology, phytochemistry and pharmacology: a successful combination in the study of Croton cajucara. PubMed: Characterization of natural resin shellac by reactive pyrolysis-gas chromatography in the presence of organic alkali. PubMed: Chemical composition and antimicrobial activity of Croton urucurana Baillon (Euphorbiaceae). PubMed: Natural-product inhibitors of human DNA ligase I. PubMed: Isolation and structural elucidation of pentacyclic triterpenoids from Maprounea africana. PubMed: Structure of (+-)-threo-9,10,16-trihydroxypalmitic acid. PubMed: Identity of maprounic acid with aleuritolic acid. Revision of the structure of maprounic acid: X-ray crystal structure of p-bromobenzyl acetylmaprounate. PubMed: Simple and economic syntheses of some (Z)-7- and (Z)-9-alkenyl acetates, and of (E,Z)-7,9-dodecadien-1-yl acetate, the sex pheromone of the European grapevine moth, using aleuritic acid as a common starting material.