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16179-44-5

16179-44-5

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16179-44-5 Usage

General Description

2-hydroxyethyl cyclohexanecarboxylate is a chemical compound with the molecular formula C9H16O3. It is commonly used as an ingredient in personal care products and cosmetics due to its moisturizing and emollient properties. 2-hydroxyethyl cyclohexanecarboxylate is derived from cyclohexane and contains a hydroxyl group, making it suitable for use in skincare formulations. It is often included in moisturizers, lotions, and creams to help improve skin hydration and softness. Additionally, 2-hydroxyethyl cyclohexanecarboxylate may also be utilized in fragrance products, as it can contribute to the overall texture and feel of the product. Overall, this chemical serves as a versatile ingredient in the formulation of cosmetic and personal care products.

Check Digit Verification of cas no

The CAS Registry Mumber 16179-44-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,7 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16179-44:
(7*1)+(6*6)+(5*1)+(4*7)+(3*9)+(2*4)+(1*4)=115
115 % 10 = 5
So 16179-44-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O3/c10-6-7-12-9(11)8-4-2-1-3-5-8/h8,10H,1-7H2

16179-44-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxyethyl cyclohexanecarboxylate

1.2 Other means of identification

Product number -
Other names Cyclohexancarbonsaeure-(1)-<2-hydroxy-ethylester>

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:16179-44-5 SDS

16179-44-5Downstream Products

16179-44-5Relevant articles and documents

An intracrystalline catalytic esterification reaction between ethylene glycol intercalated layered double hydroxide and cyclohexanecarboxylic acid

Wang, Hao,Duan, Weizhuo,Lei, Yanqing,Wu, Yan,Guo, Ke,Wang, Xiaodong

, p. 44 - 47 (2015)

An intracrystalline catalytic esterification between ethylene glycol intercalated NiAl layered double hydroxide and cyclohexanecarboxylic acid is developed. It leads to much higher deacidification efficiency than the bulk catalytic reaction. The intracrys

Al2O3/MeSO3H (AMA) as a new reagent with high selective ability for monoesterification of diols

Sharghi, Hashem,Sarvari, Mona Hosseini

, p. 3627 - 3633 (2007/10/03)

A new facile method for monoesterification of diols has been developed. A variety of diols, in particular oligoethylene glycols, were selectively monoesterified in excellent yields by reaction with aromatic and aliphatic acids in the presence of Al2O3/MeSO3H as a new reagent without use of any solvents.

Oxidative ring cleavage of cyclic acetals with hypervalent tert-butylperoxy-λ3-iodanes

Sueda, Takuya,Fukuda, Sonoko,Ochiai, Masahito

, p. 2387 - 2390 (2007/10/03)

(matrix presented) Exposure of cyclic acetals to 1-tert-butylperoxy-1,2-benziodoxol-3(1H)-one in the presence of tert-butyl hydroperoxide and potassium carbonate in benzene at room temperature results in oxidative ring cleavage to glycol monoesters via intermediate tert-butylperoxy ortho esters.

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