sennidin A

dihydroxydianthrone

CAS: 641-12-3 C30 H18 O10 MW: 538.46546000

Identification

Namesennidin A
IUPAC(9R)-9-[(9R)-2-carboxy-4,5-dihydroxy-10-oxo-9H-anthracen-9-yl]-4,5-dihydroxy-10-oxo-9H-anthracene-2-carboxylic acid
CAS Number641-12-3
EINECS211-371-5
FDA UNIIO8793FIM31
Molecular FormulaC30 H18 O10
Molecular Weight538.46546000
MDL NumberMFCD00017368
Nikkaji NumberJ562.021J

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 801.80 °C. @ 760.00 mm Hg (est)
Flash Point 847.00 °F. TCC ( 452.60 °C. ) (est)
logP (o/w) 8.240 (est)
Soluble in water, 0.0007279 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 sennidin A usage levels up tonot for fragrance use.
Recommendation for sennidin A flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

found in nature

Synonyms

(9,9'- bianthracene)-2,2'-dicarboxylic acid, 9,9',10,10'-tetrahydro-4,4',5,5'-tetrahydroxy-10,10'-dioxo-, (R*,R*)-(+)- (9R)-9-[(9R)-2- carboxy-4,5-dihydroxy-10-oxo-9H-anthracen-9-yl]-4,5-dihydroxy-10-oxo-9H-anthracene-2-carboxylic acid dihydroxydianthrone (R*,R*)-(+)-9,9',10,10'- tetrahydro-4,4',5,5'-tetrahydroxy-10,10'-dioxo(9,9'-bianthracene)-2,2'-dicarboxylic acid PubMed: Necrosis targeted combinational theragnostic approach using radioiodinated Sennidin A in rodent tumor models. PubMed: Sennidin stimulates glucose incorporation in rat adipocytes. PubMed: The influence of the sennosides on absorption of glycyrrhetic acid in rats. PubMed: A sennoside-hydrolyzing beta-glucosidase from Bifidobacterium sp. strain SEN is inducible. PubMed: Isolation of a human intestinal anaerobe, Bifidobacterium sp. strain SEN, capable of hydrolyzing sennosides to sennidins. PubMed: The senna drug and its chemistry.