Welcome to LookChem.com Sign In|Join Free
  • or
2,2'-Oxydipropanol, also known as Bis(1-methyl-2-hydroxyethyl) Ether, is a colorless oil that is a metabolite formed during the aerobic degradation of polypropylene glycol by Corynebacterium species. It is also found in smoke condensate from nonfiltered cigarettes.

108-61-2

Post Buying Request

108-61-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

108-61-2 Usage

Uses

Used in Chemical Industry:
2,2'-Oxydipropanol is used as a chemical intermediate for the synthesis of various compounds and materials due to its ether functional group and hydroxyl groups.
Used in Pharmaceutical Industry:
2,2'-Oxydipropanol is used as a solvent or a starting material in the production of pharmaceutical compounds, taking advantage of its solubility and reactivity.
Used in Cosmetics Industry:
2,2'-Oxydipropanol is used as a solvent in the formulation of cosmetics, providing a means to dissolve and stabilize other ingredients in the product.
Used in Environmental Research:
2,2'-Oxydipropanol is utilized in studies related to environmental chemistry and pollution, particularly in the analysis of smoke condensates and their effects on health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 108-61-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 108-61:
(5*1)+(4*0)+(3*8)+(2*6)+(1*1)=42
42 % 10 = 2
So 108-61-2 is a valid CAS Registry Number.

108-61-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-hydroxypropan-2-yloxy)propan-1-ol

1.2 Other means of identification

Product number -
Other names 1,2-Dipropylene glycol

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:108-61-2 SDS

108-61-2Relevant academic research and scientific papers

RSV ANTIVIRAL COMPOUNDS

-

Page/Page column 47, (2014/05/07)

Inhibitors of RSV replication of formula RI including stereochemically isomeric forms, and salts or solvates thereof, wherein R22, W, Q, V, Z p,s,and Het have the meaning as defined herein. The present invention also relates to processes for preparing said compounds, pharmaceutical compositions containing them and their use, alone or in combination with other RSV inhibitors, in RSV therapy.

APPLICATIONS OF BIOBASED GLYCOL COMPOSITIONS

-

Page/Page column 11-14, (2008/06/13)

A biobased replacement for propylene glycol and ethylene glycol derived from petrochemical sources is presented. The product mixture from the hydrogenolysis of certain polyols from biobased renewable resources may replace propylene glycol and ethylene glycol products from petrochemical sources. Applications and methods of the biobased hydrogenolysis product mixture are disclosed. The compositions and methods provide a feedstock for industrial use which has a 13C/12C isotope ratio characteristic of bioderived material.

Oxidation process

-

Page/Page column 4, (2008/06/13)

A process is disclosed for reacting an olefin, hydrogen, and oxygen in a reactor in the presence of an epoxidation catalyst comprising a transition metal zeolite and a noble metal to produce a product stream comprising an epoxide and an alkane. The alkane is separated and oxidized to at least one oxygenated product.

Direct epoxidation process

-

Page/Page column 6-7, (2008/06/13)

A process is disclosed for reacting an olefin, hydrogen, and oxygen in a reactor in the presence of a catalyst comprising a transition metal zeolite and a noble metal to produce a reaction mixture comprising an epoxide and acidic byproducts. A portion of the reaction mixture is contacted with an adsorbent so that a treated mixture having a reduced amount of byproducts is produced. The treated mixture is recycled back to the reactor. Including an adsorption step should improve the catalyst productivity and epoxide selectivity.

Direct epoxidation process

-

Page/Page column 4-5, (2008/06/13)

A process is disclosed for the epoxidation of an olefin with hydrogen and oxygen in the presence of an oxidation catalyst comprising a transition metal zeolite, and a noble metal catalyst comprising a noble metal and an ion-exchange resin. The process is highly productive and selective in making epoxides. A noble metal catalyst comprising a cation-exchanged resin further improves the productivity and/or the selectivity of the process.

Direct epoxidation process

-

Page/Page column 5, (2008/06/13)

A process is disclosed for the epoxidation of an olefin with hydrogen and oxygen in the presence of an oxidation catalyst comprising a transition metal zeolite and a polymer-encapsulated noble metal catalyst. The noble metal catalyst comprises a noble metal and an ion-exchange resin. The process using the polymer-encapsulated noble metal catalyst gives higher epoxide productivity than a process that uses a noble metal catalyst which is not encapsulated by a polymer.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 108-61-2