(1beta,2alpha,4alpha)-p-menth-2-yl hexanoate

Base Information

  • Chemical Name: (1beta,2alpha,4alpha)-p-menth-2-yl hexanoate
  • CAS No.: 6070-16-2

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What is the (1beta,2alpha,4alpha)-p-menth-2-yl hexanoate ?

(1beta,2alpha,4alpha)-p-menth-2-yl hexanoate is , while it's Molecular Formula is C16 H30 O2 . Used in Food and Beverage Industry:
(1beta,2alpha,4alpha)-p-menth-2-yl hexanoate is used as a flavoring agent for its fruity and minty aroma, enhancing the taste and smell of various food and beverage products.
Used in Perfume and Fragrance Industry:
(1beta,2alpha,4alpha)-p-menth-2-yl hexanoate is used in the production of perfumes and fragrances due to its pleasant and refreshing scent, contributing to the overall appeal and attractiveness of these products.

What is the CAS number for (1beta,2alpha,4alpha)-p-menth-2-yl hexanoate ?

The CAS number of (1beta,2alpha,4alpha)-p-menth-2-yl hexanoate is 6070-16-2.

More information of (1beta,2alpha,4alpha)-p-menth-2-yl hexanoate 6070-16-2 are:

CAS?Number

6070-16-2

Molecular Formula

C16 H30 O2

Molecular Weight

254.413

Density

0.91g/cm3

Boiling Point

294.2°Cat760mmHg

Flash Point

139.9°C

PSA

26.30000

LogP

4.57070

What is (1beta,2alpha,4alpha)-p-menth-2-yl hexanoate (6070-16-2) used for?

(1beta,2alpha,4alpha)-p-Menth-2-yl hexanoate is a naturally occurring ester compound derived from the essential oil of peppermint (Mentha piperita). It is characterized by its unique molecular structure, with a p-menthane skeleton and a hexanoate functional group. (1beta,2alpha,4alpha)-p-menth-2-yl hexanoate is known for its pleasant, minty aroma and is widely used in the fragrance and flavor industries. It can be found in various applications, such as perfumes, cosmetics, and food products, where it imparts a refreshing and cooling sensation. The chemical structure of (1beta,2alpha,4alpha)-p-menth-2-yl hexanoate consists of a p-menthane backbone with a hexanoate ester group attached to the 2-position, giving it its distinct properties and applications.

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