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29623-83-4

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29623-83-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29623-83-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,6,2 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29623-83:
(7*2)+(6*9)+(5*6)+(4*2)+(3*3)+(2*8)+(1*3)=134
134 % 10 = 4
So 29623-83-4 is a valid CAS Registry Number.

29623-83-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(2-cyanoethyl)phosphinic acid

1.2 Other means of identification

Product number -
Other names -

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:29623-83-4 SDS

29623-83-4Downstream Products

29623-83-4Relevant articles and documents

Aluminum-organophosphorus hybrid nanorods for simultaneously enhancing the flame retardancy and mechanical properties of epoxy resin

Jiajun, Ma,Junxiao, Yang,Yawen, Huang,Ke, Cao

, p. 2007 - 2017 (2012)

New aluminum-organophosphorus hybrid nanorods (AOPH-NR) have been prepared by reacting aluminum hydroxide (ATH) with dibenzylphosphinic acid (DBPA) with aluminum hydroxide (ATH) and used to prepare nanocomposites with epoxy resin. In order to determine the structure-property relationship of these composites, several other phosphinic acids of the general formula (R(CH2) n)2POOH (R = ester, allyl, nitrile, n = 1 or 2), and corresponding AOPHs were synthesized. FTIR, Raman, TGA, and XRD examinations showed that only AOPH-NR possesses a highly hybrid structure and high thermostability. SEM and TEM confirmed the nanorod morphology of AOPH-NR. The formation mechanism can be described as a decomposing-reforming process. This characteristic causes AOPH-NR to exhibit superior properties. Limiting oxygen index (LOI) determination and cone calorimeter analysis showed that the incorporation of only 4.25 wt% AOPH-NR remarkably improved the LOI value to as much as 28.0 and led to a 23% reduction in peak heat release rate (PHRR). Dynamic mechanical analysis (DMA) indicated that the mechanical properties of epoxy resin were also improved by incorporating AOPH-NR. In this way, the aluminum-organophosphorus hybridization via reacting ATH with specific organophosphinic acids shows promise as a means of improving flame retardancy and mechanical properties simultaneously. The thermal and anti-flaming properties of composites, combined with the properties of AOPHs, allowed us to discover the important role that the release and migration of phosphorus species plays in fire-retarding materials. This provides a new insight into the design of high-performance flame retardants.

ORGANIC PHOSPHORUS COMPOUNDS 101. PREPARATION AND PHYSICAL PROPERTIES OF BIS(AMINOALKYL)PHOSPHINIC ACIDS

Maier, Ludwig

, p. 67 - 72 (2007/10/02)

The synthesis, physical and spectroscopic properties of 3-aminopropyl-aminomethylphosphinic acid, 5, bis(2-aminoethyl)phosphinic acid, 8, and of bis(3-aminopropyl)phosphinic acid, 10, are reported. Key words: 3-Aminopropyl-aminomethylphosphinic acid; bis(

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