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140-25-0

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140-25-0 Usage

Description

BENZYL LAURATE is an emollient ester derived from the reaction of benzyl alcohol and lauric acid. It is known for its easy emulsification, silky skin feel, and non-toxic, non-irritating properties. BENZYL LAURATE is also characterized by its non-viscous and non-oily nature, making it a versatile ingredient in various applications.

Uses

Used in Cosmetics and Personal Care Industry:
BENZYL LAURATE is used as an emollient for providing a smooth and silky texture to the skin. Its non-oily and non-viscous properties make it an ideal ingredient for formulations that require a light and non-greasy feel.
Used in Skincare Products:
BENZYL LAURATE is used as a skin conditioning agent for its ability to improve the skin's softness and smoothness without causing oiliness or greasiness.
Used in Hair Care Products:
BENZYL LAURATE is used as a hair conditioning agent to provide a smooth and silky feel to the hair, making it easier to comb and style.
Used in Sunscreen Products:
BENZYL LAURATE is used as a solubilizer for sunscreen actives, enhancing their stability and performance in the formulation.
Used in Mineral Oil Reduction:
BENZYL LAURATE is used to reduce the oiliness of mineral oil, providing a more comfortable and less greasy feel to the user.

Safety Profile

A skin irritant. When heated to decomposition it emits acrid smoke andirritating fumes.

Check Digit Verification of cas no

The CAS Registry Mumber 140-25-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 140-25:
(5*1)+(4*4)+(3*0)+(2*2)+(1*5)=30
30 % 10 = 0
So 140-25-0 is a valid CAS Registry Number.
InChI:InChI=1/C19H30O2/c1-2-3-4-5-6-7-8-9-13-16-19(20)21-17-18-14-11-10-12-15-18/h10-12,14-15H,2-9,13,16-17H2,1H3

140-25-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzyl Laurate

1.2 Other means of identification

Product number -
Other names benzyl dodecanoate

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:140-25-0 SDS

140-25-0Relevant articles and documents

-

Mohler,Polya

, p. 96,100 (1937)

-

Tunable aryl imidazolium ionic liquids (TAIILs) as environmentally benign catalysts for the esterification of fatty acids to biodiesel fuel

Ho, Wen-Yueh,Lin, Wesley,Lin, Yi-Jyun,Luo, Shun-Yuan,Pantawane, Amit,Su, Po-Fang,Thul, Mayur,Tseng, Shao-An,Wu, Hsin-Ru

, (2020/12/02)

Herein, we describe the synthesis of tunable aryl imidazolium ionic liquid catalysts and tested for esterification of fatty acids to biodiesel. In this work, six tunable aryl imidazolium ionic liquids (TAIILs) 1a-1f were prepared. These ionic liquids were used as the economical and reusable catalysts for the synthesis of biodiesel fuels. The reaction has been preceded in a monophase at 80 °C for 4 h, after which the product was separated from the catalyst system by a simple liquid/liquid phase separation at room temperature with excellent yields. With the simple post-process, the catalyst is reusable at least 6 times. This novel method offers a short reaction time, good yields, and environmentally benign characteristics.

NiH-Catalyzed Reductive Relay Hydroalkylation: A Strategy for the Remote C(sp3)?H Alkylation of Alkenes

Zhou, Fang,Zhu, Jin,Zhang, Yao,Zhu, Shaolin

supporting information, p. 4058 - 4062 (2018/03/21)

The terminal-selective, remote C(sp3)?H alkylation of alkenes was achieved by a relay process combining NiH-catalyzed hydrometalation, chain walking, and alkylation. This method enables the construction of unfunctionalized C(sp3)?C(sp3) bonds under mild conditions from two simple feedstock chemicals, namely olefins and alkyl halides. The practical value of this transformation is further demonstrated by the large-scale and regioconvergent alkylation of isomeric mixtures of olefins at low catalyst loadings.

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