40853-55-2 Usage
Description
ACETIC ACID 2-ISOPROPYL-5-METHYLHEXYL ESTER, also known as isopropyl myristate, is a versatile chemical compound that serves as a solvent in various industrial and commercial applications. It is recognized for its wide-ranging uses and is considered safe for use when proper handling and disposal procedures are followed.
Uses
Used in Cosmetic Industry:
ACETIC ACID 2-ISOPROPYL-5-METHYLHEXYL ESTER is used as an emollient for its ability to soften and smooth the skin, providing a pleasant texture and improving the overall appearance of cosmetic products.
Used in Food Industry:
ACETIC ACID 2-ISOPROPYL-5-METHYLHEXYL ESTER is used as a flavoring ingredient to enhance the taste and aroma of various food products, contributing to a more enjoyable consumer experience.
Used in Plastic and Rubber Manufacturing:
ACETIC ACID 2-ISOPROPYL-5-METHYLHEXYL ESTER is used as a lubricant in the manufacturing process of plastic and rubber products, facilitating smoother production and improving the quality of the final products.
Check Digit Verification of cas no
The CAS Registry Mumber 40853-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,8,5 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40853-55:
(7*4)+(6*0)+(5*8)+(4*5)+(3*3)+(2*5)+(1*5)=112
112 % 10 = 2
So 40853-55-2 is a valid CAS Registry Number.
40853-55-2Relevant articles and documents
Model Studies of Terpene Biosynthesis. Intermolecular 1'-2 Electrophilic Condensation of 3-Methyl-2-butenyl Acetate
King, Chi-Hsin R.,Poulter, C. Dale
, p. 1413 - 1420 (2007/10/02)
The stereochemistry of the carbon-carbon bond-forming step in the electrophilic intermolecular 1'-2 condensation of 3-methyl-2-butenyl acetate (1-OAc) to yield lavandulyl acetate (2-OAc) was studied.Treatment of (1S)-3-methyl-2-butenyl acetate ((1S)-1-OAc) with aluminum trichloride in ethyl acetate gave labeled lavandulyl acetate (2-OAc) (30percent) and isoprene (65percent) as the major products.The configurations at C(1), C(2), and C(3) and the relative abundances of the diastereomers of 1-OAc were determined by converting the mixture to 3-(2'-propyl)-butyrolactone (3).The intensities of 1H resonances characteristic of each diastereomer were measured with the aid of Pirkle's chiral shift reagent, (S)-(+)-2,2,2-trifluoro-1-(9-anthryl)ethanol.The analysis showed that equal amounts of the (1S,2S,3R), (1S,2R,3R), (1S,2S,3S), and (1S,2R,3S) diastereomers of 2-OAc were obtained, signifying that the 1'-2 condensation was stereorandom at C(1) of the electrophilic isoprene unit.
