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63906-10-5

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63906-10-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63906-10-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,9,0 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63906-10:
(7*6)+(6*3)+(5*9)+(4*0)+(3*6)+(2*1)+(1*0)=125
125 % 10 = 5
So 63906-10-5 is a valid CAS Registry Number.

63906-10-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hexadecylpyridin-1-ium-3-carboxamide,chloride

1.2 Other means of identification

Product number -
Other names 1-Cetyl-3-carbamidopyridiniumchloride

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:63906-10-5 SDS

63906-10-5Downstream Products

63906-10-5Relevant articles and documents

Mechanisms of Transmembrane Electron Transfer: Diffusion of Uncharged Redox Forms of Viologen, 4,4'-Bipyridine, and Nicotinamide with Long Alkyl Chains

Hammarstroem, Leif,Almgren, Mats,Lind, Johan,Merenyi, Gabor,Norrby, Thomas,Akermark, Bjoern

, p. 10083 - 10091 (1993)

Transmembrane electron transfer in lecithin (phosphatidylcholine) vesicles was studied by pulse radiolysis.Upon reduction, cetylmethylviologen (N-hexadecyl-N'-methyl-4,4'-bipyridinium, CMV), cetylbipyridine (4-(N-hexadecylpyridinium-4-yl)pyridine, CB), and cetylnicotinamide (N-hexadecyl-3-(aminocarbonyl)pyridinium, CNA) transferred electrons from the bulk water phase to Fe(CN)63- in the internal water phase of the vesicles.The transmembrane electron transfer was found in all cases to proceed through diffusion of uncharged forms of the redox mediators (CMV0, CB0, and CNA0, respectively) but the kinetic behavior varied considerably.The mechanisms for CB and CNA were simple, the reaction following first-order kinetics, and the transmembrane diffusion was rate limiting (k = (1.5 +/- 0.3) * 103 s-1 for CB and k = 3.2 +/- 0.5 s-1 for CNA).The machanism for CMV was more complicated, and the reaction followed second-order kinetics.The rate-determining step was proposed to be the disproportionation of two viologen radicals formed by the radiation pulse (2CMV+ CMV0 + CMV2+), followed by rapid transmembrane diffusion of CMV0 and its subsequent reoxidation by Fe(CN)63-.In pulse radiolysis, and in phosphorescence quenching experiments with Pt2(P2O5)4H84-, CB0 and CB+ were used as models in order to obtain the rates of transmembrane diffusion of CMV0 and CMV+, respectively.Our results exclude the possibility of electron tunneling between viologens on opposite sides of the membrane, and they provide strong arguments against transmembrane diffusion of viologen radical (CMV+).

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