83921-02-2

Basic information

• Product Name: 7-hydroxy-α-terpineol
• Synonyms: 7-hydroxy-α-terpineol
• CAS NO: 83921-02-2
• Molecular Weight: 170.252
• Mol File: 83921-02-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 7-hydroxy-α-terpineol(CAS DataBase Reference)
• NIST Chemistry Reference: 7-hydroxy-α-terpineol(83921-02-2)
• EPA Substance Registry System: 7-hydroxy-α-terpineol(83921-02-2)

Safety Data

• Hazardous Substances Data: 83921-02-2(Hazardous Substances Data)

Upstream product

• 7785-53-7 4R-α-terpineol 
• 177698-19-0 Beta-pinene 
• 875-08-1 (-)-2,10-epoxypinane 

Downstream Products

• 65221-01-4 7-acetoxy-p-menth-1-en-8-ol 
• 57717-97-2 (R)-Perillyl alcohol 

Relevant articles and documents

Biotransformation of α-terpineol by: Alternaria alternata

α-Terpineol (1), the main volatile constituent in some traditional Chinese medicines, has been reported to be metabolized to 4R-oleuropeic acid by the larvae of common cutworms. The present study verified that α-terpineol could be converted to 4R-oleurope

THE ENANTIOSELECTIVE BIOTRANSFORMATION OF α-TERPINEOL AND ITS ACETATE WITH THE CULTURED CELLS OF NICOTIANA TABACUM

In the biotransformation of the enantiomers of p-ment-1-en-8-ol (α-terpineol) and 8-acetoxy-p-ment-1-ene (α-terpinyl acetate) with the cultured suspension cells of Nicotina tabacum, it was clarified that the cultured cells effected the hydroxylation at the 6-position of (4R)-(+)-enantiomer in preference to the (4S)-(-)-enantiomer, whereas the cells did the hydrolysis of the acetoxyl group and the hydroxylation of the ethylenic linkage of (4S)-(-)-α-terpinyl acetate in preference to the (4R)-(+)-enantiomer.