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1 Material Safety Data Sheet. 2 Structure and properties. ... Dow Chemical. Archived from the original (PDF) on 27 September 2007. Distillation data Vapor–liquid ...
Diisopropanolamine is a chemical compound with the molecular formula C 6 H 15 NO 2, used as an emulsifier, stabilizer, and chemical intermediate. [2] Diisopropanolamine can be prepared by the reaction of isopropanolamine or ammonia with propylene oxide. [3] Synthesis of diisopropanolamine from isopropanolamine
Table data obtained from Lange's Handbook of Chemistry, 10th ed. Specific gravity is at 15 °C, referenced to water at 15 °C. See details on: Freezing Points of Glycerine-Water Solutions Dow Chemical [6] or Freezing Points of Glycerol and Its Aqueous Solutions. [7]
Propylene glycol methyl ether acetate (PGMEA, 1-methoxy-2-propanol acetate) is a P-type glycol ether used in inks, coatings, and cleaners. It is sold by Dow Chemical under the name Dowanol PMA, [3] by Shell Chemical under the name methyl proxitol acetate, [4] [5] and by Eastman under the name PM Acetate.
Triton X-100 (C 14 H 22 O(C 2 H 4 O) n) is a nonionic surfactant that has a hydrophilic polyethylene oxide chain (on average it has 9.5 ethylene oxide units) and an aromatic hydrocarbon lipophilic or hydrophobic group.
A History of the Dow Chemical Physics Lab: The Freedom to be Creative. M. Dekker. ISBN 0-8247-8097-3. E. Ned Brandt. (2003). Growth Company: Dow Chemical's First Century. Michigan State University Press. ISBN 0-87013-426-4 online book review; Don Whitehead and Max Dendermonde. (1968). The Dow Story: The History of the Dow Chemical Co. McGraw-Hill.
While cleaning laboratory glassware, he came across a vial he could not scrub clean. Dow researchers made this material into a greasy, dark green film, [4] first called "Eonite" and then "Saran". [3] [5] Ralph Wiley went on to become one of Dow Chemical's research scientists and invent and develop many plastics, chemicals and production machines.
In the process developed by Dow Chemical, glycerol undergoes two substitution reactions when treated with hydrogen chloride in the presence of a carboxylic acid catalyst. This is the same intermediate formed in the allyl chloride/hypochlorous acid process, and is likewise then treated with base to form epichlorohydrin.
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