aleuritic acid
hexadecanoic acid, 9,10,16-trihydroxy-
None found
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9,10,16-trihydroxyhexadecanoic acid (Click)
CAS Number: 6949-98-0Picture of molecule
Nikkaji Web: J21.879K
MDL: MFCD00021797
XlogP3-AA: 2.50 (est)
Molecular Weight: 304.42704000
Formula: C16 H32 O5
NMR Predictor: Predict (works with chrome or firefox)
Category: cosmetic ingredient for skin conditioning
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Soluble in:
 water, 110.6 mg/L @ 25 °C (est)
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Organoleptic Properties:
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: skin conditioning
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 None found
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Safety Information:
Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: cosmetic ingredient for skin conditioning
Recommendation for aleuritic acid usage levels up to:
 not for fragrance use.
Recommendation for aleuritic acid flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 10790
National Institute of Allergy and Infectious Diseases: Data
 9,10,16-trihydroxyhexadecanoic acid
Chemidplus: 0006949980
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 9,10,16-trihydroxyhexadecanoic acid
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 10790
Pubchem (sid): 135054194
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Other Information:
(IUPAC): Atomic Weights of the Elements 2009
(IUPAC): Atomic Weights of the Elements 2009 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
HMDB (The Human Metabolome Database): Search
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
RSC Learn Chemistry: View
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Potential Blenders and core components note
None Found
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 found in nature
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 aleuritolic acid
 hexadecanoic acid, 9,10,16-trihydroxy-
9,10,16-trihydroxyhexadecanoic acid
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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.
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