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22048-97-1

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22048-97-1 Usage

General Description

Leptomerine is a chemical compound that is often used as a surfactant and wetting agent in various industrial applications. It is a non-ionic and highly effective emulsifier, which helps to improve the dispersibility and stability of oil-in-water emulsions. Leptomerine is also known for its excellent detergency and foaming properties, making it a popular ingredient in cleaning products such as detergents and soaps. Additionally, its low toxicity and biodegradability make it a preferred choice in the formulation of environmentally friendly and sustainable products. Overall, Leptomerine plays a crucial role in enhancing the performance and efficiency of many commercial and consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 22048-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,4 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22048-97:
(7*2)+(6*2)+(5*0)+(4*4)+(3*8)+(2*9)+(1*7)=91
91 % 10 = 1
So 22048-97-1 is a valid CAS Registry Number.

22048-97-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name leptomerine

1.2 Other means of identification

Product number -
Other names 1-Methyl-2-propyl-1H-chinolon-4

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:22048-97-1 SDS

22048-97-1Downstream Products

22048-97-1Relevant articles and documents

BF3*OEt2 CATALYZED CYCLOADDITION REACTIONS OF N-ARYL SCHIFF'S BASES WITH 1-ALKENYL, 1,2-PROPADIENYL, AND 1-ALKYNYL SULFIDES

Narasaka, Koichi,Shibata, Takanori

, p. 1039 - 1053 (2007/10/02)

Cycloaddition reaction proceeds between N-aryl Schiff's bases and 1-allenyl sulfides, a 1,2-propadienyl sulfide, or 1-alkynyl sulfides in the presence of BF3*OEt2 to provide 2-substituted quinoline derivatives.A 2-alkyl-4-quinolone alkaloid, leptome

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