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51805-99-3

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51805-99-3 Usage

General Description

2,4,4-trimethyl-2-pentyl-1,3-oxazolidine is a chemical compound that belongs to the class of oxazolidines, which are cyclic organic compounds containing an oxazolidine ring. It is commonly used as a stabilizer in the formulation of personal care products such as shampoos, conditioners, and lotions. It functions as a fragrance ingredient and is also added to cosmetics to prevent them from spoiling or deteriorating. 2,4,4-trimethyl-2-pentyl-1,3-oxazolidine helps to extend the shelf life of these products and improve their overall quality. Additionally, it is known for its antimicrobial properties, which further contributes to its use in personal care and cosmetic formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 51805-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,8,0 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51805-99:
(7*5)+(6*1)+(5*8)+(4*0)+(3*5)+(2*9)+(1*9)=123
123 % 10 = 3
So 51805-99-3 is a valid CAS Registry Number.

51805-99-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,4-trimethyl-2-pentyl-1,3-oxazolidine

1.2 Other means of identification

Product number -
Other names Oxazolidine,2,4,4-trimethyl-2-pentyl

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:51805-99-3 SDS

51805-99-3Relevant articles and documents

Selective formation of aminoxyls or oxaziridines by oxidation of 2,2,4,4-tetrasubstituted oxazolidines

Hamdani, Mourad,Scholler, Denise,Bouquant, James,Feigenbaum, Alexandre

, p. 605 - 616 (2007/10/03)

The reactivity of 2,2,4,4-tetrasubstituted-1,3-oxazolidines 1 with m-chloroperbenzoic acid was reinvestigated. Aminoxyls 5 are isolated in good yields in ether at -15°C, or in anhydrous dichloromethane at 0°C. Oxaziridines 4 are promoted at room temperature, or in the presence of an acid. In any case, short reaction times prevented the degradation of aminoxyls and oxaziridines. The competition between oxaziridines 4 and aminoxyls 5 is ruled by the oxazolidine imine equilibrium.

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