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83350-56-5

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83350-56-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83350-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,3,5 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 83350-56:
(7*8)+(6*3)+(5*3)+(4*5)+(3*0)+(2*5)+(1*6)=125
125 % 10 = 5
So 83350-56-5 is a valid CAS Registry Number.

83350-56-5SDS

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 1-dodecylpyridin-1-ium-4-carboxamide,bromide

1.2 Other means of identification

Product number -
Other names 4-carbamoyl-1-dodecylpyridin-1-ium bromide

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:83350-56-5 SDS

83350-56-5Downstream Products

83350-56-5Relevant articles and documents

The wide-spectrum antimicrobial effect of novel N-alkyl monoquaternary ammonium salts and their mixtures; the QSAR study against bacteria

Benkova, Marketa,Bostik, Pavel,Bostikova, Vanda,Dolezal, Rafael,Gunde-Cimerman, Nina,Hobzova, Lenka,Hympanova, Michaela,Jun, Daniel,Korabecny, Jan,Malinak, David,Marek, Jan,Markova, Aneta,Prchal, Lukas,Ryskova, Lenka,Salajkova, Sarka,Sleha, Radek,Soukup, Ondrej,Sep?i?, Kristina

, (2020/08/26)

Quaternary ammonium salts (QASs) have been widely used for disinfection purposes because of their low price, high efficacy and low human toxicity for decades. However, precise mechanisms of action nor the powerful versatile agent against all antimicrobial

Ion Exchange in Micellar Solutions. 7. Effect of Detergent Structure on the Binding and Reactivity of OH- in Cationic Micellar Solutions

Bonilha, Joao B. S.,Chiericato, Glaico,,Martins-Franchetti, Sandra M.,Ribaldo, Edson J.,Quina, Frank H.

, p. 4941 - 4947 (2007/10/02)

Ion exchange selectivity coefficients for the binding of OH- to a series of homologous alkyltrimethylammonium bromides and chlorides and to hexadecylpyridinium chloride (HPCl) and bromide are reported.The magnitude of these selectivity coefficients is determined principally by the nature of the detergent counterion (Cl- or Br-).Although there appear to be secondary contributions from the head group type, variations in the detergent alkyl chain length (tetradecyl to octadecyl) have little or no effet on the observed OH- binding affinity.Quantitative analysis of kinetic data for a series of alkaline hydrolysis reactions in micellar HPCl provides intrinsic reactivity parameters in the micellar pseudophase which are in all cases comparable to those in micellar hexadecyltrimethylammonium bromide (CTAB).It is concluded that the factors which contribute to the binding and to the reactivity of OH- at the cationic micellar surface are distinct and that the intrinsic effects of nonfunctionalized cationic detergents on reactivity and equilibria are quite similar (as opposed to being highly surfactant specific).

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