110-34-9

Usage

Uses

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.

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

Upstream product

• 78-83-1 2-methyl-propan-1-ol 
• 112-67-4 n-hexadecanoyl chloride 
• 119520-62-6 palmitic acid-(4-nitro-anilide) 
• 57-10-3 1-hexadecylcarboxylic acid 
• 112-39-0 hexadecanoic acid methyl ester 

Downstream Products

• 57-10-3 1-hexadecylcarboxylic acid 

Relevant academic research and scientific papers

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

In the present study, eleven new sex-specific components extracted from female rectal gland of olive fruit flies were synthesized and identified. The quantitative determination of those components by GC and GC/EI-MS, at different moments of the insect life span, highlighted the growing trend of their secretion. While for the synthesis of saturated esters, conventional transesterification methods could be adopted, for the synthesis of unsaturated components, a Negishi cross-coupling between organozinc halides and (Z)-1-bromo-1-alkenes was developed. To the extent of our knowledge, this reaction represents the first example of supported-catalyst promoted Negishi coupling, between an alkylzinc reagent and an alkenyl halide.

USE OF ENDOCANNABINOID-LIKE COMPOUNDS FOR TREATING CNS DEGENERATIVE DISORDERS

no abstract published

An eco-friendly method for the synthesis of aryl and alkyl esters of carboxylic acids using acid activated Indian bentonite

Esterification of various carboxylic acids with phenol and alcohols has been achieved using acid activated Indian bentonite (AAIB) as catalyst. The catalyst is versatile, and the reaction is found to work well for primary, secondary and tertiary alcohols. The yields are very good under specific reaction conditions.

THE INVENTION OF RADICAL REACTIONS PART XVIII. A CONVENIENT SOLUTION TO THE 1-CARBON PROBLEM (R-CO2H --> R-13CO2H)

Radicals generated by photolysis (W light) of esters derived from N-hydroxy-2-thiopyridone react with electrophilic isocyanides 2a and (in the presence of trifluoroacetic acid) 2b to give adducts of type 3.Convenient reaction procedures have been worked out to hydrolyse the adducts to amides of type 5, from which the original acid can be regenerated under mild conditions.The three important acids oleic, linoleic and arachidonic have all given smooth reactions.In suitable examples, quantitative evolution of carbon dioxide and incorporation of 13C without dilution have been demonstrated.This reaction sequence will be useful for the labelling in the carboxyl group of prostaglandins, leukotrienes, and the side chain carboxyls of peptides.