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1-benzyl-1-azoniabicyclo[2.2.2]octane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42790-41-0

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42790-41-0 Usage

Type of Compound

Quaternary ammonium compound

Primary Uses

Disinfectant, antiseptic, preservative in pharmaceuticals, and surfactant in industrial and agricultural applications

Effectiveness

Kills a wide range of bacteria, fungi, and viruses

Popularity

Common ingredient in cleaning and personal care products

Safety

Generally considered safe for use

Potential Risks

Prolonged or excessive exposure can cause skin and eye irritation and has been associated with potential health risks

Usage Guidelines

Follow recommended usage guidelines to minimize harmful effects

Check Digit Verification of cas no

The CAS Registry Mumber 42790-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,7,9 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 42790-41:
(7*4)+(6*2)+(5*7)+(4*9)+(3*0)+(2*4)+(1*1)=120
120 % 10 = 0
So 42790-41-0 is a valid CAS Registry Number.

42790-41-0SDS

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 1-benzyl-1-azoniabicyclo[2.2.2]octane

1.2 Other means of identification

Product number -
Other names -

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:42790-41-0 SDS

42790-41-0Downstream Products

42790-41-0Relevant academic research and scientific papers

Delineation of the factors governing reactivity and selectivity in epoxide formation from ammonium ylides and aldehydes

Robiette, Raphael,Conza, Matteo,Aggarwal, Varinder K.

, p. 621 - 623 (2007/10/03)

Diastereoselectivity in reactions of aryl-stabilised ammonium ylides are highly sensitive to the nature of the amine and the ylide substituent. DFT calculations are consistent with a mechanism in which reversibility in betaine formation [despite the high energy (and therefore instability) of ammonium ylides] is finely balanced due to the high barrier to ring closure. The Royal Society of Chemistry.

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