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4,8-dimethyl-6,6-bis{[methyl(methylcarbamoyl)amino]methyl}-3,9-dioxo-2,4,8,10-tetraaza-6-phosphoniaundecane chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69248-03-9

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69248-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69248-03-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,4 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69248-03:
(7*6)+(6*9)+(5*2)+(4*4)+(3*8)+(2*0)+(1*3)=149
149 % 10 = 9
So 69248-03-9 is a valid CAS Registry Number.

69248-03-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name tetrakis[[methyl(methylcarbamoyl)amino]methyl]phosphanium,chloride

1.2 Other means of identification

Product number -
Other names Phosphonium,tetrakis((methyl((methylamino)carbonyl)amino)methyl)-,chloride

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:69248-03-9 SDS

69248-03-9Relevant academic research and scientific papers

CONDENSATION OF TETRAKIS(HYDROXYMETHYL)PHOSPHONIUM SULFATES AND SULFONATES WITH 1,3-DIMETHYLUREA

Frank, Arlen W.

, p. 207 - 212 (2007/10/02)

An unexpected displacement of one of the phosphorus groups occured when the chloride 1a was replaced by the sulfate 1b in its reactions with 1,3-dimethylurea.The products, 2c and 5c, were bisulfates rather than sulfates.In contrast, no displacement occurr

SYNTHESIS AND PROPERTIES OF CONDENSED UREIDOMETHYL PHOSPHONIUM SALTS

Frank, Arlen W.

, p. 147 - 152 (2007/10/02)

Urea, N-methylurea, and 1,3-dimethylurea react with tetrakis(hydroxymethylphosphonium chloride (THPC) in molar ratios lower than 4:1, forming condensed quaternary ureidomethyl phosphonium salts.The urea and N-methylurea products are polymeric gels, whereas the 1,3-dimethylurea products are cyclic crystalline solids.Some of the phosphonium salts are interconvertible through condensation or displacement reactions.Hydrolysis of the phosphonium salts, followed by oxidation, yields tertiary phosphine oxides having similar properties.The products were characterized by IR, NMR, an d electron spectroscopy for chemical analysis (ESCA).

Quaternary ureidomethyl phosphonium salts

-

, (2008/06/13)

Novel quaternary ureidomethyl phosphonium salts having the general formula STR1 are prepared by condensing a urea having the formula RNHC(O)NR'R" with a quaternary hydroxymethyl phosphonium salt having the formula (HOCH2)4 P+ X- in a molar ratio of at least 2:1. The products, which are characterized by the absence of residual hydroxymethyl groups, are useful as finishing agents for imparting flame retardant properties to cotton fabrics.

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