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1-(diethoxyphosphoryl)butyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40568-81-8

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40568-81-8 Usage

Chemical class

Organophosphorus compounds

Physical state

Colorless liquid

Uses

Plasticizer, solvent in industrial applications, flame retardant in plastics and rubber manufacturing

Toxicity

Moderately toxic if ingested or inhaled

Hazards

Can cause skin and eye irritation

Safety

Handle with caution, follow proper safety protocols

Check Digit Verification of cas no

The CAS Registry Mumber 40568-81-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,5,6 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40568-81:
(7*4)+(6*0)+(5*5)+(4*6)+(3*8)+(2*8)+(1*1)=118
118 % 10 = 8
So 40568-81-8 is a valid CAS Registry Number.

40568-81-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-diethoxyphosphorylbutyl acetate

1.2 Other means of identification

Product number -
Other names 1-Acetoxy-butylphosphonsaeure-diethylester

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:40568-81-8 SDS

40568-81-8Relevant academic research and scientific papers

An efficient route to chiral α- and β-hydroxyalkanephosphonates

Pamies, Oscar,Baeckvall, Jan-E.

, p. 4815 - 4818 (2007/10/03)

Enzymatic kinetic resolution of α- and β-hydroxyphosphonates in combination with ruthenium-catalyzed alcohol isomerization led to a successful dynamic kinetic resolution. A variety of racemic hydroxyphosphonates were efficiently transformed to the corresponding enantiomerically pure acetates (ee up to 99% and yield up to 87%).

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