28384-26-1 Usage
Description
1-(2,6,6-trimethyl-1-cyclohexen-1-yl)butan-1-one, commonly known as patchouli alcohol, is a chemical compound derived from the essential oil of the patchouli plant. It is a ketone with a complex molecular structure and a strong, distinct odor that is characterized by earthy, woody, and musky notes. Patchouli alcohol is valued for its unique scent and potential medicinal properties.
Uses
Used in Fragrance Industry:
1-(2,6,6-trimethyl-1-cyclohexen-1-yl)butan-1-one is used as a base note in the fragrance industry for its strong, distinct, and long-lasting earthy, woody, and musky scent. It is a key component in perfumes, colognes, and other scented products, providing depth and richness to the overall fragrance.
Used in Cosmetics and Personal Care Products:
In the cosmetics and personal care industry, 1-(2,6,6-trimethyl-1-cyclohexen-1-yl)butan-1-one is used as a key ingredient in the production of various products such as soaps, lotions, and creams. Its unique scent and potential antimicrobial properties make it a valuable addition to these products.
Used in Medicinal Applications:
Patchouli alcohol has been studied for its potential medicinal properties, including its antimicrobial and anti-inflammatory effects. It is being explored as a possible treatment for various conditions due to these properties, although further research is needed to fully understand its therapeutic potential.
Check Digit Verification of cas no
The CAS Registry Mumber 28384-26-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,3,8 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28384-26:
(7*2)+(6*8)+(5*3)+(4*8)+(3*4)+(2*2)+(1*6)=131
131 % 10 = 1
So 28384-26-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H22O/c1-5-7-11(14)12-10(2)8-6-9-13(12,3)4/h5-9H2,1-4H3
28384-26-1Relevant articles and documents
In tandem or alone: A remarkably selective transfer hydrogenation of alkenes catalyzed by ruthenium olefin metathesis catalysts
Zieliski, Grzegorz Krzysztof,Samojlowicz, Cezary,Wdowik, Tomasz,Grela, Karol
supporting information, p. 2684 - 2688 (2015/04/14)
A system for transfer hydrogenation of alkenes, composed of a ruthenium metathesis catalyst and HCOOH, is presented. This operationally simple system can be formed directly after a metathesis reaction to effect hydrogenation of the metathesis product in a single-pot. These hydrogenation conditions are applicable to a wide range of alkenes and offer remarkable selectivity. This journal is
