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66411-63-0

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66411-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66411-63-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,4,1 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66411-63:
(7*6)+(6*6)+(5*4)+(4*1)+(3*1)+(2*6)+(1*3)=120
120 % 10 = 0
So 66411-63-0 is a valid CAS Registry Number.

66411-63-0SDS

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-butanoyloxy-3-octadecanoyloxypropyl) octadecanoate

1.2 Other means of identification

Product number -
Other names Glyceryl 2-butyrate distearate

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:66411-63-0 SDS

66411-63-0Downstream Products

66411-63-0Relevant articles and documents

Preparation of low calorie structured lipids catalyzed by 1,5,7-triazabicyclo[4.4.0]dec-5-ene(TBD)-functionalized mesoporous SBA-15 silica in a heterogeneous manner

Xie, Wenlei,Qi, Cong

, p. 3348 - 3355 (2014)

1,5,7-Triazabicyclo[4.4.0]dec-5-ene (TBD, a strong bicyclic guanidine base) functionalized SBA-15 material has been found to be an efficient solid catalyst for the interesterification between tributyrin and methyl stearate in a solvent-free system for the production of low-calorie structured lipid (LCSL). The solid base catalyst was characterized by using small-angle X-ray scattering, Fourier transform infrared spectra, thermo gravimetric analysis, scanning electron microscopy, transmission electron microscopy, nitrogen adsorption-desorption, and elemental analysis techniques. The obtained LCSL was analyzed by reverse-phase high-performance liquid chromatography for triacylglycerol composition. The influence of various reaction parameters, such as the substrate ratio, reaction temperature, and reaction time, on the interesterification reaction was investigated systematically. More than 90% LCSL was obtained at 80°C within 1 h when the methyl stearate/tributyrin molar ratio of 2:1 was employed. The obtained solid catalyst could be recovered easily and reused for several recycles with a negligible loss of activity. By using the solid base catalyst, an eco-friendly more benign process for the interesterification reaction in a heterogeneous manner was developed.

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