queretaroic acid

3beta,30-dihydroxyolean-12-en-28-oic acid

CAS: 511-82-0 C30 H48 O4 MW: 472.70936000

Identification

Namequeretaroic acid
CAS Number511-82-0
FDA UNIISearch
Molecular FormulaC30 H48 O4
Molecular Weight472.70936000
Nikkaji NumberJ14.007D

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Soluble in water, 0.003427 mg/L @ 25 °C (est)

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

Categorynatural substances and extractives
Recommendation for queretaroic acid usage levels up tonot for fragrance use.
Recommendation for queretaroic acid flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

chenopodium quinoa stenocereus thurberi

Synonyms

3beta,30- dihydroxyolean-12-en-28-oic acid (2S,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10- hydroxy-2-(hydroxymethyl)-2,6a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid PubMed: Clerodendrum serratum (L.) Moon. - a review on traditional uses, phytochemistry and pharmacological activities. PubMed: Biotransformation of oleanolic and maslinic acids by Rhizomucor miehei. PubMed: Variation in saponin content during the growing season of spotted medic [Medicago arabica (L.) Huds.]. PubMed: Triterpenoid saponins from the seeds of Pharbitis nil. PubMed: Hydroxylation of oleanolic acid to queretaroic acid by cytochrome P450 from Nonomuraea recticatena. PubMed: Inhibitory effect of some triterpenes from cacti on 32Pi-incorporation into phospholipids of HeLa cells promoted by 12-O-tetradecanoylphorbol-13-acetate.