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100694-13-1

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100694-13-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100694-13-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,6,9 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 100694-13:
(8*1)+(7*0)+(6*0)+(5*6)+(4*9)+(3*4)+(2*1)+(1*3)=91
91 % 10 = 1
So 100694-13-1 is a valid CAS Registry Number.

100694-13-1SDS

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 HYPOXANTHINE MONOHYDROCHLORIDE, H

1.2 Other means of identification

Product number -
Other names HYPOXANTHINE MONOHYDROCHLORIDE,[8-3H]

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:100694-13-1 SDS

100694-13-1Downstream Products

100694-13-1Relevant articles and documents

Real-Time Monitoring of Enzyme-Catalysed Reactions using Deep UV Resonance Raman Spectroscopy

Westley, Chloe,Fisk, Heidi,Xu, Yun,Hollywood, Katherine A.,Carnell, Andrew J.,Micklefield, Jason,Turner, Nicholas J.,Goodacre, Royston

, p. 6983 - 6987 (2017)

For enzyme-catalysed biotransformations, continuous in situ detection methods minimise the need for sample manipulation, ultimately leading to more accurate real-time kinetic determinations of substrate(s) and product(s). We have established for the first time an on-line, real-time quantitative approach to monitor simultaneously multiple biotransformations based on UV resonance Raman (UVRR) spectroscopy. To exemplify the generality and versatility of this approach, multiple substrates and enzyme systems were used involving nitrile hydratase (NHase) and xanthine oxidase (XO), both of which are of industrial and biological significance, and incorporate multistep enzymatic conversions. Multivariate data analysis of the UVRR spectra, involving multivariate curve resolution-alternating least squares (MCR-ALS), was employed to effect absolute quantification of substrate(s) and product(s); repeated benchmarking of UVRR combined with MCR-ALS by HPLC confirmed excellent reproducibility.

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