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PALMITIC ACID ISOBUTYL ESTER

Basic Information

  • CAS No.: 110-34-9

Physical properties

Product Description

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What is the PALMITIC ACID ISOBUTYL ESTER ?

PALMITIC ACID ISOBUTYL ESTER is , while it's Molecular Formula is C20H40O2. Used in Cosmetic and Personal Care Industry:
PALMITIC ACID ISOBUTYL ESTER is used as a fragrance ingredient for its pleasant scent and ability to enhance the sensory experience of cosmetic and personal care products.
Used in Skincare Products:
PALMITIC ACID ISOBUTYL ESTER is used as a moisturizing agent in emollient creams and lotions to improve the skin's texture and appearance, providing hydration and nourishment.
Used in Industrial Applications:
PALMITIC ACID ISOBUTYL ESTER is used as a solvent and emollient in the production of specialty chemicals and lubricants, contributing to the efficiency and performance of various industrial processes.

What is the CAS number for PALMITIC ACID ISOBUTYL ESTER ?

The CAS number of PALMITIC ACID ISOBUTYL ESTER is 110-34-9.

More information of PALMITIC ACID ISOBUTYL ESTER 110-34-9 are:

Synonyms

Palmiticacid, isobutyl ester (7CI,8CI);Isobutyl hexadecanoate;Isobutyl palmitate;Kessco IBP;Palmitic acid, isobutyl ester;

CAS?Number

110-34-9

Molecular Formula

C20H40O2

Molecular Weight

312.536

Density

0.862 g/cm3

Melting Point

19 °C

Boiling Point

354.6 °C at 760 mmHg

Flash Point

170.9 °C

HS CODE

2915709000

PSA

26.30000

LogP

6.66690

What is PALMITIC ACID ISOBUTYL ESTER (110-34-9) used for?

PALMITIC ACID ISOBUTYL ESTER is a chemical compound derived from palmitic acid, a saturated fatty acid. It is known for its moisturizing properties and is commonly used as a fragrance ingredient in cosmetic and personal care products. The isobutyl ester form of palmitic acid contributes to improving the skin's texture and appearance, making it a versatile compound for both cosmetic and industrial applications.

InChI:InChI=1/C20H40O2/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20(21)22-18-19(2)3/h19H,4-18H2,1-3H3

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Article

Source

Identification and synthesis of new sex-specific components of olive fruit fly (Bactrocera oleae) female rectal gland, through original Negishi reactions on supported catalysts

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