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
140-25-0Relevant articles and documents
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Mohler,Polya
, p. 96,100 (1937)
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Visible-light induced metal-free cascade Wittig/hydroalkylation reactions
Miao, Pannan,Li, Ruining,Lin, Xianfeng,Rao, Liangming,Sun, Zhankui
, p. 1638 - 1641 (2021/03/09)
Cascade reactions are green and powerful transformations for building multiple carbon-carbon bonds in one step. Through a relay olefination and radical addition process, we were able to develop the cascade Wittig/hydroalkylation reactions induced by visible light. This metal-free radical approach features mild conditions, robustness, and excellent functionality compatibility. It allows access to saturated C3 homologation products directly from aldehydes or ketones. The synthetic utility of this method is demonstrated by a two-step synthesis ofindolizidine 209D.
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.