toddaculin

2H-1-benzopyran-2-one, 5,7-dimethoxy-6-(3-methyl-2-butenyl)-

CAS: 4335-12-0 C16 H18 O4 MW: 274.31626000

Identification

Nametoddaculin
IUPAC5,7-dimethoxy-6-(3-methylbut-2-enyl)chromen-2-one
CAS Number4335-12-0
FDA UNIISearch
Molecular FormulaC16 H18 O4
Molecular Weight274.31626000
Nikkaji NumberJ13.504F

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 432.81 °C. @ 760.00 mm Hg (est)
Flash Point 378.00 °F. TCC ( 192.20 °C. ) (est)
logP (o/w) 4.151 (est)
Soluble in water, 6.277 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 toddaculin usage levels up tonot for fragrance use.
Recommendation for toddaculin flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

found in nature

Synonyms

2H-1- benzopyran-2-one, 5,7-dimethoxy-6-(3-methyl-2-butenyl)- 5,7- dimethoxy-6-(3-methyl-2-butenyl)-2H-1-benzopyran-2-one 5,7- dimethoxy-6-(3-methylbut-2-enyl)chromen-2-one toddaculine PubMed: Toddaculin, Isolated from of Toddalia asiatica (L.) Lam., Inhibited Osteoclastogenesis in RAW 264 Cells and Enhanced Osteoblastogenesis in MC3T3-E1 Cells. PubMed: Anti-inflammatory activity of omphalocarpin isolated from Radix Toddaliae Asiaticae. PubMed: Toddaculin, a natural coumarin from Toddalia asiatica, induces differentiation and apoptosis in U-937 leukemic cells. PubMed: [Studies on the chemical constituents of Rutaceae++ plants. LXVI. The chemical constituents of Toddalia asiatica (L.) Lam. (T. aculeata Pers.). (1). Chemical constituents of the root bark].