mansonone C

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1,2-naphthalenedione, 3,8-dimethyl-5-(1-methylethyl)-

CAS: 5574-34-5 C15 H16 O2 MW: 228.29092000
All Ingredients Aromatic Ingredients CAS Numbers Found in Nature

Identification

Namemansonone C
IUPAC3,8-dimethyl-5-propan-2-ylnaphthalene-1,2-dione
CAS Number5574-34-5
FDA UNIISearch
Molecular FormulaC15 H16 O2
Molecular Weight228.29092000
Nikkaji NumberJ13.432E

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 367.90 °C. @ 760.00 mm Hg (est)
Flash Point 307.00 °F. TCC ( 152.90 °C. ) (est)
logP (o/w) 3.870 (est)
Soluble in water, 3.252 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 mansonone C usage levels up tonot for fragrance use.
Recommendation for mansonone C flavor usage levels up tonot for flavor use.

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5574-34-5 3,8-dimethyl-5-propan-2-ylnaphthalene-1,
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Potential Uses

None Found

Natural Occurrence

mansonia gagei wood

Synonyms

3,8- dimethyl-5-(1-methyl ethyl)-1,2-naphthalene dione 3,8- dimethyl-5-isopropyl-1,2-naphthoquinone 3,8- dimethyl-5-propan-2-ylnaphthalene-1,2-dione 1,2- naphthalenedione, 3,8-dimethyl-5-(1-methylethyl)- PubMed: Acetyl- and butyryl-cholinesterase inhibitory activities of mansorins and mansonones. PubMed: Use of allylic strain to enforce stereochemistry. Direct syntheses of 7,8-dihydroxycalamenene and mansonone C. PubMed: Antifungal, antioxidant and larvicidal activities of compounds isolated from the heartwood of Mansonia gagei. PubMed: Effects of mansonones on lipid peroxidation, P450 monooxygenase activity, and superoxide anion generation by rat liver microsomes.