2,3,3a,5,6,7,8,8a-octahydro-1,4-dimethyl-7-prop-1-en-2-yl-1H-azulen-4-ol

CAS: 21698-41-9 C15 H26 O MW: 222.37142000

Identification

Namepogostol
IUPAC1,4-dimethyl-7-prop-1-en-2-yl-2,3,3a,5,6,7,8,8a-octahydro-1H-azulen-4-ol
CAS Number21698-41-9
FDA UNIISearch
Molecular FormulaC15 H26 O
Molecular Weight222.37142000
Nikkaji NumberJ55.656D

Regulatory

Physical Properties

Assay 90.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 303.00 to 304.00 °C. @ 760.00 mm Hg
Vapor Pressure 0.000083 mmHg @ 25.00 °C. (est)
Flash Point 263.00 °F. TCC ( 128.33 °C. )
logP (o/w) 4.965 (est)
Soluble in alcohol
Insoluble in water

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 pogostol usage levels up tonot for fragrance use.
Recommendation for pogostol flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

FR patchouli

Natural Occurrence

patchouli oil @ 0.44% Data sage oil dalmatian @ 8.30% Data

Synonyms

1,4- dimethyl-7-prop-1-en-2-yl-2,3,3a,5,6,7,8,8a-octahydro-1H-azulen-4-ol 2,3,3a,5,6,7,8,8a- octahydro-1,4-dimethyl-7-prop-1-en-2-yl-1H-azulen-4-ol PubMed: Pogostol biosynthesis by the endophytic fungus Geniculosporium. PubMed: Chemical composition and antimicrobial activity of three essential oils from Curcuma wenyujin. PubMed: Quantitative and physical evaluation of patchouli essential oils obtained from different sources of Pogostemon cablin. PubMed: Guaiane sesquiterpenes from Biscogniauxia nummularia featuring potent antigerminative activity. PubMed: Synthesis of the reported structure of pogostol and a total aynthesis of (+/-)-kessane without the use of protecting groups. PubMed: Anti-emetic principles of Pogostemon cablin (Blanco) Benth.