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112-28-7

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112-28-7 Usage

General Description

3-(3-methoxypropoxy)propanol, also known as propylene glycol methyl ether, is a clear, colorless liquid solvent derived from renewable resources. It is commonly used as a solvent in coatings, inks, and cleaners due to its ability to dissolve a wide range of materials. It is also used as a coupling agent in various industrial applications, helping to mix two substances that would not otherwise combine. Additionally, 3-(3-methoxypropoxy)propanol has a low volatility and mild odor, making it a suitable option for environmentally friendly products. Overall, this chemical is valued for its solvent properties and versatility in various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 112-28-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 112-28:
(5*1)+(4*1)+(3*2)+(2*2)+(1*8)=27
27 % 10 = 7
So 112-28-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O3/c1-9-5-3-7-10-6-2-4-8/h8H,2-7H2,1H3

112-28-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3-methoxypropoxy)propan-1-ol

1.2 Other means of identification

Product number -
Other names dipropylene glycol monomethylether

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:112-28-7 SDS

112-28-7Downstream Products

112-28-7Relevant articles and documents

Reactivity of Neopentyl-Like Compounds in the Synthesis of Branched Polyethers

Dale, Johannes,Fredriksen, Siw B.

, p. 278 - 282 (2007/10/02)

Two singly branched symmetrical hexaethers have been synthesized, starting from 2-bromomethyl-2-methyl-1,3-dibromopropane, in a surprisingly efficient one-pot nucleophilic substitution reaction.It is proposed that the expected adverse neopentyl effect is compensated by favourable neighbouring-group participation involving a 'bromonium'-like four-membered-ring transition state.The corresponding trichloride also reacted cleanly, although much more slowly, while the tritosylate gave an oxetane derivative.

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