10099-57-7 Usage
Description
p-isopropylphenethyl alcohol, with the molecular formula C10H14O, is a colorless liquid characterized by its floral-like odor. It is a chemical compound that finds its niche in various industries due to its pleasant aroma and low toxicity.
Uses
Used in Fragrance and Flavor Industry:
p-isopropylphenethyl alcohol is used as a fragrance ingredient for its floral scent, enhancing the aroma profiles in perfumes and cosmetics. It contributes to the creation of pleasant and appealing scents in these products.
Used in Food and Beverage Industry:
p-isopropylphenethyl alcohol is used as a flavoring agent to impart a distinct taste and aroma to food and beverages, thereby enriching the sensory experience of consumers.
Used in Chemical Synthesis:
Beyond its direct applications, p-isopropylphenethyl alcohol serves as an intermediate in the synthesis of various other chemicals, playing a crucial role in the production of a wide range of compounds.
Overall, p-isopropylphenethyl alcohol is valued for its versatility, safety, and the enhancement it provides to the products it is incorporated into.
Check Digit Verification of cas no
The CAS Registry Mumber 10099-57-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,9 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10099-57:
(7*1)+(6*0)+(5*0)+(4*9)+(3*9)+(2*5)+(1*7)=87
87 % 10 = 7
So 10099-57-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O/c1-9(2)11-5-3-10(4-6-11)7-8-12/h3-6,9,12H,7-8H2,1-2H3
10099-57-7Relevant articles and documents
Transformations of epoxide derived from nopol over askanite-bentonite clay
Il'ina,Volcho,Korchagina,Salakhutdinov,Barkhash
, p. 1432 - 1436 (2007/10/03)
Transformations of epoxide derived from nopol in the presence of natural askanite-bentonite clay were studied. The major products of the isomerization in the cold are diols possessing a p-menthane skeleton, which are readily converted into bicyclic ethers when the reaction is carried out at room temperature.
