Ad
related to: 1 3 diphenyl propanediol 20 25 ctemu.com has been visited by 1M+ users in the past month
- Top Sale Items
Daily must-haves
Special for you
- Women's Clothing
Limited time offer
Hot selling items
- Store Locator
Team up, price down
Highly rated, low price
- Sale Zone
Special for you
Daily must-haves
- Top Sale Items
Search results
Results from the WOW.Com Content Network
1,3-Propanediol is the organic compound with the formula CH 2 (CH 2 OH) 2. This 3-carbon diol is a colorless viscous liquid that is miscible with water. Products
Neopentyl glycol (IUPAC name: 2,2-dimethylpropane-1,3-diol) is an organic chemical compound. It is used in the synthesis of polyesters , paints , lubricants , and plasticizers . When used in the manufacture of polyesters, it enhances the stability of the product towards heat, light, and water.
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
Bioseparation of 1,3-propanediol is a biochemical process for production of 1,3-propanediol (PDO). PDO is an organic compound with many commercial applications. Conventionally, PDO is produced from crude oil products such as propylene or ethylene oxide .
Allyl alcohol (IUPAC name: prop-2-en-1-ol) is an organic compound with the structural formula CH 2 =CHCH 2 OH. Like many alcohols , it is a water-soluble, colourless liquid. It is more toxic than typical small alcohols.
2-Methyl-2,4-pentanediol (MPD) is an organic compound with the formula (CH 3) 2 C(OH)CH 2 CH(OH)CH 3. This colourless liquid is a chiral diol. It is produced industrially from diacetone alcohol by hydrogenation. [4] Total European and USA production was 15000 tonnes in 2000. [5] 2-Methyl-2,4-pentanediol exists as two enantiomers, (4R)-(−) and ...
Structure of (C 3 H 6 S 2) 2, the oxidized "dimer" of 1,3-propanedithiol. [4] 1,3-Propanedithiol is used in the synthesis of tiapamil. 1,3-Propanedithiol reacts with metal ions to form dithiolates. Illustrative is the synthesis of the derivative diiron propanedithiolate hexacarbonyl upon reaction with triiron dodecacarbonyl: [5] Fe 3 (CO) 12 ...
4300mg/kg (rabbit,transdermal); [1] 1300mg/kg (rat, oral) [1] Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references
Ad
related to: 1 3 diphenyl propanediol 20 25 ctemu.com has been visited by 1M+ users in the past month