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25263-97-2

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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.

Check Digit Verification of cas no

The CAS Registry Mumber 25263-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,2,6 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 25263-97:
(7*2)+(6*5)+(5*2)+(4*6)+(3*3)+(2*9)+(1*7)=112
112 % 10 = 2
So 25263-97-2 is a valid CAS Registry Number.
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

25263-97-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylpropyl tetradecanoate

1.2 Other means of identification

Product number -
Other names isobutyl tetradecanoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:25263-97-2 SDS

25263-97-2Downstream Products

25263-97-2Relevant articles and documents

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-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.

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 myristic acid was synthesized and tested in vitro for antibacterial activity against Gram-positive and Gram-negative bacteria. All the compounds showed activity comparable to that of the standard drug, ciprofloxacin. The structural characteristics governing antibacterial activity of myristic acid derivatives was studied using QSAR methodology. The results showed that the antibacterial activity could be modeled using the topological descriptor, valence molecular connectivity index. The predictive ability of the models was cross-validated by construction of a test set. The low residual activity and high cross-validated r2 values ( rcv2 ) observed indicated the predictive ability of the developed QSAR models.

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