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4484-61-1

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4484-61-1 Usage

Appearance

Clear, colorless liquid

Odor

Mild, sweet

Usage

Solvent in various industries (pharmaceuticals, electronics, coatings), extractant in metal ion separation, stabilizer in lithium batteries, potential use in biofuel production and chemical reactions

Chemical category

Glycol ether

Properties

High solvent power, low volatility, water solubility

Precautions

Can cause skin, eye, and respiratory irritation; may have adverse effects on liver and kidneys with prolonged or repeated exposure

Check Digit Verification of cas no

The CAS Registry Mumber 4484-61-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,8 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4484-61:
(6*4)+(5*4)+(4*8)+(3*4)+(2*6)+(1*1)=101
101 % 10 = 1
So 4484-61-1 is a valid CAS Registry Number.

4484-61-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(methoxymethoxy)ethanol

1.2 Other means of identification

Product number -
Other names 2-Methoxymethoxy-aethanol

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:4484-61-1 SDS

4484-61-1Downstream Products

4484-61-1Relevant articles and documents

Transition metal complexes-catalyzed synthesis of 2,4,7,9- tetraoxadecane and homologs

Fontaine,Piette,Noels,Beaujean,Detry

, p. 3153 - 3156 (1998)

Polyether molecules are readily available from cheap acetals with a catalyst system based on ruthenium and tin(II) chloride. As a model reaction 1,3-dioxolane 2 reacts with dimethoxymethane 3 to yield 78% of 2,4,7,9- teetraoxadecane 1.

Organotin-containing composition for the stabilization of polymers of vinyl chloride

-

, (2008/06/13)

An organotin-containing composition for the stabilization of polymers or copolymers of vinyl chloride in which there is incorporated a stabilizing amount of an organotin compound containing at least two tin atoms and which is a mercapto, hydroxy or alkoxy substituted ester of a mercapto acid substituted organotin mercapto acid diester.

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