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21368-49-0

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21368-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21368-49-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,6 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 21368-49:
(7*2)+(6*1)+(5*3)+(4*6)+(3*8)+(2*4)+(1*9)=100
100 % 10 = 0
So 21368-49-0 is a valid CAS Registry Number.

21368-49-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name sulfocholine

1.2 Other means of identification

Product number -
Other names Sulfocholin

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:21368-49-0 SDS

21368-49-0Downstream Products

21368-49-0Relevant articles and documents

Borohydride-coupled HPLC-FPD instrumentation and its use in the determination off dimethylsulffonium compounds

Howard,Russell

, p. 2882 - 2887 (1997)

Novel HPLC instrumentation has been developed which employs an in-line sodium tetrahydroborate (borohydride) reaction step to generate volatile sulfur species from a variety of sulfonium compounds. Transfer of the resulting volatile sulfur-containing products into the gas phase permits them to be monitored using sulfur-specific flame photometric detection. The system has been evaluated for the determination of a collection of dimethylsulfonium compounds, comprising (dimethylsulfonio)propionate, S-methylmethionine (SMM), (dimethylsulfonio)-2-methylpropionate, dimethylsulfocholine, (dimethylsulfonio)-acetate, (dimethylsulfonio)butanoate, and (dimethylsulfonio)pentanoate. Following their separation by either cation- or anion-exchange HPLC, these compounds react in-line with the tetrahydroborate, generating dimethyl sulfide, which is then swept into a flame photometric detector. The development of chromatographic conditions for the resolution of the seven sulfonium compounds is described. In an example application of the instrumentation, the levels of SMM in parsley and cabbage were found to be 16 and 74 mmol kg-1, respectively, on a fresh weight basis.

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