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MYRISTIC ACID ISOBUTYL ESTER

  • Chemical Name: MYRISTIC ACID ISOBUTYL ESTER
  • CAS: 25263-97-2
  • Purity: 99%
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Quality Factory Supply 99% Pure MYRISTIC ACID ISOBUTYL ESTER 25263-97-2 with Efficient Delivery

  • Molecular Formula: C18H36O2
  • Molecular Weight: 284.483
  • Vapor Pressure: 0.000215mmHg at 25°C 
  • Refractive Index: 1.4350-1.4390 
  • Boiling Point: 326.5°Cat760mmHg 
  • Flash Point: 153.2°C 
  • PSA: 26.30000 
  • Density: 0.863g/cm3 
  • LogP: 5.88670 

MYRISTIC ACID ISOBUTYL ESTER(Cas 25263-97-2) Usage

General Description

Myristic acid isobutyl ester, also known as isobutyl myristate, is a chemical compound commonly used in the cosmetic and personal care industry as an emollient and conditioner. It is derived from myristic acid, a saturated fatty acid found in plant and animal oils, and isobutyl alcohol. Isobutyl myristate is known for its lightweight and non-greasy texture, making it an ideal ingredient in lotions, creams, and moisturizers. It helps to soften and smooth the skin by forming a protective barrier and reducing moisture loss. Additionally, it can also be used as a fragrance solvent in perfumes and colognes. Overall, myristic acid isobutyl ester is a versatile and beneficial chemical with various applications in the beauty and personal care industry.

InChI:InChI=1/C18H36O2/c1-4-5-6-7-8-9-10-11-12-13-14-15-18(19)20-16-17(2)3/h17H,4-16H2,1-3H3

25263-97-2 Relevant articles

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

Fusini, Graziano,Barsanti, Davide,Angelici, Gaetano,Casotti, Gianluca,Canale, Angelo,Benelli, Giovanni,Lucchi, Andrea,Carpita, Adriano

supporting information, p. 4381 - 4389 (2018/07/21)

In the present study, eleven new sex-spe...

Use of Lecitase-Ultra immobilized on styrene-divinylbenzene beads as catalyst of esterification reactions: Effects of ultrasounds

Alves, Joana S.,Garcia-Galan, Cristina,Danelli, Daiane,Paludo, Natália,Barbosa, Oveimar,Rodrigues, Rafael C.,Fernandez-Lafuente, Roberto

, p. 27 - 32 (2015/08/06)

Abstract In this work it was evaluated f...

Design, synthesis, antibacterial, and QSAR studies of myristic acid derivatives

Narasimhan, Balasubramanian,Mourya, Vishnukant,Dhake, Avinash

, p. 3023 - 3029 (2008/09/20)

A series of esters and amides of myristi...

25263-97-2 Process route

2-methyl-propan-1-ol
78-83-1

2-methyl-propan-1-ol

Ethyl myristate
124-06-1

Ethyl myristate

isobutyl tetradecanoate
25263-97-2

isobutyl tetradecanoate

Conditions
Conditions Yield
With iodine; for 8h; Inert atmosphere; Reflux;
85%
2-methyl-propan-1-ol
78-83-1

2-methyl-propan-1-ol

n-tetradecanoic acid
544-63-8

n-tetradecanoic acid

isobutyl tetradecanoate
25263-97-2

isobutyl tetradecanoate

Conditions
Conditions Yield
With sulfuric acid; Heating;
79%
With lecitase-ultra immobilized on styrene-divinylbenzene beads; In hexane; at 50 ℃; for 1h; Sonication; Enzymatic reaction;

25263-97-2 Upstream products

  • 78-83-1
    78-83-1

    2-methyl-propan-1-ol

  • 544-63-8
    544-63-8

    n-tetradecanoic acid

  • 124-06-1
    124-06-1

    Ethyl myristate

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