83846-52-0 Usage
Uses
Used in Fragrance and Cosmetic Industry:
Patchouli alcohol is used as a base note in perfumes and colognes for its earthy, woody aroma, adding depth and richness to fragrance formulations. Its unique scent profile makes it a popular choice in the fragrance and cosmetic industry.
Used in Traditional Medicine and Aromatherapy:
Due to its antifungal and antibacterial properties, patchouli alcohol is utilized in traditional medicine and aromatherapy for its potential therapeutic benefits.
Used as a Fixative in Fragrance Formulations:
Patchouli alcohol is also used as a fixative in fragrance formulations, helping to prolong the scent's longevity on the skin or other surfaces.
Check Digit Verification of cas no
The CAS Registry Mumber 83846-52-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,8,4 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83846-52:
(7*8)+(6*3)+(5*8)+(4*4)+(3*6)+(2*5)+(1*2)=160
160 % 10 = 0
So 83846-52-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H28O/c1-11(18)12-6-8-17(5)14-10-15(2,3)13(14)7-9-16(12,17)4/h12-14H,6-10H2,1-5H3
83846-52-0Relevant academic research and scientific papers
Perfume compositions and perfumed articles containing one or more tetramethyl-tri-cycloundecyl-alkyl ketones as perfume base
-
, (2008/06/13)
Perfume compositions, perfumed materials and perfumed articles containing one or more isomers of substituted 1.4.4.8-tetramethyl-tricyclo[6.3.0.02.5 ]-undecanes as perfume base. Use of one or more isomers of 9-alkanoyl-1.4.4.8-tetramethyl-tricyclo[6.3.0.02.5 ]undecanes having formula STR1 wherein R is methyl, ethyl or n-propyl as a perfume component in perfume compositions and in imparting fragrance to materials and articles for example soaps, cleaning preparations and cosmetic preparations.
A NOVEL RADICAL INDUCED REARRANGEMENT OF THE CARYOPHYLLENE SKELETON
Linde, L. M. van der,Weerdt, A. J. A. van der
, p. 1201 - 1204 (2007/10/02)
The addition of an acetyl radical on caryophyllene leads to formation of the four isomeric ketones 5-8 involving a novel rearrangement of the caryophyllene skeleton.
