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Sulfoxylic diamide, N,N'-dimethyl-N,N'-bis(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53370-29-9

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53370-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53370-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,7 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53370-29:
(7*5)+(6*3)+(5*3)+(4*7)+(3*0)+(2*2)+(1*9)=109
109 % 10 = 9
So 53370-29-9 is a valid CAS Registry Number.

53370-29-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[benzyl(methyl)amino]sulfanyl-N-methyl-1-phenylmethanamine

1.2 Other means of identification

Product number -
Other names Bis-(N-benzyl-N-methylamino)-sulfid

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:53370-29-9 SDS

53370-29-9Relevant academic research and scientific papers

Synthesis of the first poly(diaminosulfide)s and an investigation of their applications as drug delivery vehicles

Yoo, Jun,D'Mello, Sheetal R.,Graf, Tyler,Salem, Aliasger K.,Bowden, Ned B.

experimental part, p. 688 - 697 (2012/07/13)

This paper reports the first examples of poly(diaminosulfide)s that were synthesized by the reaction of a sulfur transfer reagent and several secondary diamines. The diaminosulfide group has the general structure of R 2N-S-NR2, and although it has been used in the synthesis of small molecules, it has never been utilized in the synthesis of macromolecules until this report. A series of poly(diaminosulfide)s were synthesized at elevated temperatures, and the molecular weights of the polymers were as high as 12-400 g mol-1 with conversions for the polymerization reaction up to 99%. The rate constants for the transamination reactions that lead to the polymers were measured in several solvents to provide an understanding of the reaction conditions necessary to polymerize the monomers. The degradation of diaminosulfides was studied in D2O, C6D6, CD3OD, CDCl3, and DMSO-d 6/D2O to demonstrate that they were very stable in organic solvents but degraded within hours under aqueous conditions. These results clearly demonstrated that diaminosulfides are very stable in organic solvents under ambient conditions. Poly(diaminosulfide)s have sufficient stabilities to be useful for many applications. The ability of these polymers to function as drug delivery vehicles was studied by the fabrication of nanoparticles of a water-insoluble poly(diaminosulfide) with a dye. The microparticles were readily absorbed into human embryonic 293 cells and possessed no measurable toxicity toward these same cells.

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