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461-55-2

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461-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 461-55-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 461-55:
(5*4)+(4*6)+(3*1)+(2*5)+(1*5)=62
62 % 10 = 2
So 461-55-2 is a valid CAS Registry Number.

461-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name butanoate

1.2 Other means of identification

Product number -
Other names N-Butyrate

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:461-55-2 SDS

461-55-2Relevant articles and documents

Microbial electrosynthesis of butyrate from carbon dioxide

Ganigué,Puig,Batlle-Vilanova,Balaguer,Colprim

, p. 3235 - 3238 (2015)

This work proves for the first time the bioelectrochemical production of butyrate from CO2 as a sole carbon source. The highest concentration of butyrate achieved was 20.2 mMC, with a maximum butyrate production rate of 1.82 mMC d-1. The electrochemical characterisation demonstrated that the CO2 reduction to butyrate was hydrogen driven. Production of ethanol and butanol was also observed opening up the potential for biofuel production.

Direct deamination of primary amines by water to produce alcohols

Khusnutdinova, Julia R.,Ben-David, Yehoshoa,Milstein, David

supporting information, p. 6269 - 6272 (2013/07/19)

Just add water! The title reaction is catalyzed by an acridine-based pincer complex (1, see scheme). This one-step transformation uses water as the only reagent in the absence of additional bases, oxidants, or reductants. Cyclization of 1,4-diaminobutane and 1,6-diaminohexane catalyzed by 1 leads to the formation of pyrrolidine and azepane, respectively. Copyright

p-octiphenyl β-barrels with ion channel and esterase activity

Baumeister, Bodo,Sakai, Naomi,Matile, Stefan

, p. 4229 - 4232 (2007/10/03)

(Metrix Presented) Design, synthesis, and esterase and ion channel activity of a novel barrel-stave supramolecule with hydrophobic exterior and histidine-rich interior are reported. Voltage-dependent binding of pyrenyl-8-oxy-1,3,6-trisulfonates by histidi

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