35897-13-3 Usage
Uses
Used in Flavor and Fragrance Industry:
3-METHYLPENTYL ACETATE is used as a flavoring agent for its characteristic banana-like aroma, enhancing the taste and scent profiles of various food products.
Used in Food Industry:
3-METHYLPENTYL ACETATE is used as an artificial flavoring to impart a fruity note to foods, particularly those seeking to emulate the taste of bananas or other related fruits.
Used in Chemical Production:
3-METHYLPENTYL ACETATE is used as a key ingredient in the production of solvents, adhesives, and coatings, contributing to the manufacturing process of these products due to its versatile chemical properties.
Used in Cosmetics and Personal Care Products:
3-METHYLPENTYL ACETATE is used as a fragrance component in cosmetics and personal care products to provide a fresh and fruity scent, enhancing the sensory experience for consumers.
Safety Considerations:
It is important to handle 3-METHYLPENTYL ACETATE with care due to its flammable nature and potential to cause skin and eye irritation, ensuring proper safety measures are in place during its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 35897-13-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,9 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35897-13:
(7*3)+(6*5)+(5*8)+(4*9)+(3*7)+(2*1)+(1*3)=153
153 % 10 = 3
So 35897-13-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O2/c1-4-7(2)5-6-10-8(3)9/h7H,4-6H2,1-3H3
35897-13-3Relevant academic research and scientific papers
Complete structures of the sphingosine analog mycotoxins fumonisin B1 and AAL toxin T(A): Absolute configuration of the side chains
Shier,Abbas,Badria
, p. 1571 - 1574 (2007/10/02)
Fumonisin B1 and AAL toxin T(A) are sphingosine-analog mycotoxins characterized by propane-1,2,3-tricarboxylic acid side chains esterified to alkylamine backbones. The absolute configuration of all stereogenic centers in the backbones is known. Using chiral gas chromatography methodology we have determined the absolute configuration at C-3' in the side chains to the S, thereby completing structure determination of both toxins.
