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1,3-Propanediol, 2-(1,1-dimethylethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73757-68-3

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73757-68-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73757-68-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,5 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73757-68:
(7*7)+(6*3)+(5*7)+(4*5)+(3*7)+(2*6)+(1*8)=163
163 % 10 = 3
So 73757-68-3 is a valid CAS Registry Number.

73757-68-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2-methylpropan-2-yl)oxy]propane-1,3-diol

1.2 Other means of identification

Product number -
Other names 1,3-Propanediol,2-(1,1-dimethylethoxy)

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:73757-68-3 SDS

73757-68-3Relevant academic research and scientific papers

Understanding the surface and structural characteristics of tungsten oxide supported on tin oxide catalysts for the conversion of glycerol

Srinivas,Raveendra,Parameswaram,Sai Prasad,Loridant,Lingaiah

, p. 897 - 908 (2015/08/04)

Abstract Catalysts with varying WO3 content on SnO2 were prepared and characterized by X-ray diffraction, in situ Raman spectroscopy, X-ray photoelectron spectroscopy and temperature programmed desorption of NH3. In situ Raman analysis reveals the presence isolated monomers and polymeric species of WO3. These catalysts were evaluated for the conversion of glycerol into value added chemicals. Etherification of glycerol with tertiary butanol and preparation of glycerol carbonate from glycerol and urea are studied over these catalysts. The catalytic activity results suggest that the glycerol conversion and selectivity depends on the morphology of WO3 which in turn is related to its content in the catalyst. The catalysts with 5 wt.% of WO3 on SnO2 resulted in high dispersion with larger number of strong acidic sites. The selectivity in the glycerol etherification is related to the nature of the catalyst and reaction time. These catalysts also exhibited high activity for synthesis of glycerol carbonate. The effect of various reaction parameters was studied to optimize the reaction conditions. The catalysts also exhibited consistent activity upon reuse.

Catalytic synthesis of glycerol tert-butyl ethers as fuel additives from the biodiesel by-product glycerol

Huang, Rui,Kim, Eui Yong

, (2015/05/27)

Glycerol is a major by-product in the biodiesel production process. Every 100 kg of biodiesel produced generates approximately 10 kg of crude glycerol. As the biodiesel industry has expanded rapidly in recent years, finding new uses of the excess crude glycerol is important. Many studies have examined alternative uses of crude glycerol. One of them is the use of glycerol derivatives, such as glycerol tert-butyl ethers as fuel additives. In this paper, the etherification kinetics of glycerol with tert-butyl alcohol to glycerol tert-butyl ethers was studied using an Amberlyst catalyst. The influences of the catalyst type and loading, reaction time, molar ratio, and temperature were investigated in detail.

Catalytic production of oxygenated additives by glycerol etherification

Cannilla, Catia,Bonura, Giuseppe,Frusteri, Leone,Frusteri, Francesco

, p. 1248 - 1254 (2014/08/05)

In this work the etherification reaction of glycerol with isobutene (IB) and tert-butyl alcohol (TBA) has been studied with the aim of preparing mixtures with high content of poly-substituted ethers. The results obtained using solid acid catalysts have shown that the reaction with IB proceeds at a high rate but the formation of undesired di-isobutene (DIB) represents a serious problem when catalysts with high density of acid sites, such as Amberlyst, are used. When using TBA as a reactant, the main problem is the formation of water that, due to thermodynamic reasons, prevents the formation of poly-substituted ethers regardless of the catalyst used. Some preliminary experiments carried out with a water permselective tubular membrane have demonstrated that the yield of poly-substituted ethers significantly increases once water was selectively removed from the reaction medium by recirculation of the gas phase. [Figure not available: see fulltext.]

Thermodynamic characteristics of the sorption of glycerol ethers on stationary phase OV-101

Zhabina,Krasnykh,Levanova

, p. 1590 - 1593 (2014/10/16)

Retention characteristics, temperature dependences of the retention characteristics, and thermodynamic characteristics of sorption on the nonpolar OV-101 phase are determined for 33 glycerol mono-, di-, and triethers with linear and branched monobasic alc

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