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Sodium butyl, also known as sodium butoxide or sodium n-butoxide, is an organic compound with the chemical formula C4H9ONa. It is a colorless, hygroscopic solid that is soluble in water and organic solvents. Sodium butyl is derived from the reaction of butanol with sodium hydroxide and is commonly used as a catalyst in various chemical reactions, particularly in the production of esters and amides. It is also employed as a base in organic synthesis and as a curing agent for epoxy resins. Due to its strong basic nature, it is essential to handle sodium butyl with caution, as it can cause irritation to the skin, eyes, and respiratory system.

3525-44-8

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3525-44-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3525-44-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,2 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3525-44:
(6*3)+(5*5)+(4*2)+(3*5)+(2*4)+(1*4)=78
78 % 10 = 8
So 3525-44-8 is a valid CAS Registry Number.

3525-44-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,butane

1.2 Other means of identification

Product number -
Other names Sodium,butyl

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:3525-44-8 SDS

3525-44-8Upstream product

3525-44-8Relevant academic research and scientific papers

Alkali metal-containing, organometallic products

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, (2008/06/13)

An alkali metal-containing, organometallic product, which is hydrocarbon-soluble, is prepared by reacting an organo-alkali metal reactant in which the alkali metal atom is bonded to a carbon atom, e.g. cyclohexyl-lithium, with a di(organooxy)-alkaline earth metal reactant, e.g. di-n-butoxy-magnesium, in an organic solvent at about -20° to +120°C. The organo-alkali metal reactant can be prepared by reacting an organo halide with an alkali metal, and this can be done in situ, i.e. in the presence of the di(organooxy)-alkaline earth metal reactant. The organometallic product has approximately the same chemical reactivity as the organo-alkali metal reactant from which it is prepared, but is more soluble in hydrocarbon solvents.

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