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91337-36-9

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91337-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91337-36-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,3 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 91337-36:
(7*9)+(6*1)+(5*3)+(4*3)+(3*7)+(2*3)+(1*6)=129
129 % 10 = 9
So 91337-36-9 is a valid CAS Registry Number.

91337-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dibutoxypropan-1-ol

1.2 Other means of identification

Product number -
Other names 1-Propanol,2,3-dibutoxy

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:91337-36-9 SDS

91337-36-9Downstream Products

91337-36-9Relevant articles and documents

Heterogeneous catalytic conversion of glycerol with n-butyl alcohol

Samoilov,Ramazanov,Nekhaev,Maksimov

, p. 125 - 130 (2016/04/20)

The etherification of glycerol with n-butyl alcohol at 140°C in the presence of sulfonated cation-exchange resins and zeolite catalysts in an autoclave reactor has been studied. It has been shown that styrene - divinylbenzene ion-exchange resins are effective catalysts for the production of glycerol n-butyl ethers: the glycerol conversion is about 98% with an n-butyl ether selectivity of about 88 mol % (140°C, 5 h, 5 wt % Amberlyst 36 catalyst, and 10 wt % glycerol in n-butanol). Zeolites Y and β in the H+ form exhibit comparable specific activity (glycerol conversion of no more than 25% under similar conditions) in combination with high selectivity for glycerol di-n-butyl ethers (up to 28%).

POLYOL ETHERS AND PROCESS FOR MAKING THEM

-

Page/Page column 8, (2010/03/31)

New polyol ether compounds and a process for their preparation. The process comprises reacting a polyol, a carbonyl compound, and hydrogen in the presence of hydrogenation catalyst, to provide the polyol ether. The molar ratio of polyol to carbonyl compound in the process is greater than 5:1.

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