Welcome to LookChem.com Sign In|Join Free
  • or
2,4,4-trimethyl-2-pentyl-1,3-oxazolidine is a cyclic organic compound belonging to the class of oxazolidines, characterized by the presence of an oxazolidine ring. It is recognized for its stabilizing, antimicrobial, and fragrance-enhancing properties, making it a valuable ingredient in various formulations.

51805-99-3

Post Buying Request

51805-99-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

51805-99-3 Usage

Uses

Used in Personal Care Products:
2,4,4-trimethyl-2-pentyl-1,3-oxazolidine is used as a stabilizer in the formulation of personal care products such as shampoos, conditioners, and lotions. It helps to extend the shelf life of these products and improve their overall quality by preventing spoilage or deterioration.
Used in Cosmetics:
In the cosmetics industry, 2,4,4-trimethyl-2-pentyl-1,3-oxazolidine is used as a fragrance ingredient to enhance the scent profile of products. Its antimicrobial properties also contribute to maintaining the integrity and safety of cosmetic formulations, ensuring their effectiveness and consumer satisfaction.

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 academic research and scientific papers

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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 51805-99-3