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hexanedioic acid - benzene-1,4-diyldimethanamine (1:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13534-24-2

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13534-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13534-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,3 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13534-24:
(7*1)+(6*3)+(5*5)+(4*3)+(3*4)+(2*2)+(1*4)=82
82 % 10 = 2
So 13534-24-2 is a valid CAS Registry Number.

13534-24-2SDS

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 [4-(aminomethyl)phenyl]methanamine,hexanedioic acid

1.2 Other means of identification

Product number -
Other names [4-(aminomethyl)phenyl]methanamine

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:13534-24-2 SDS

13534-24-2Downstream Products

13534-24-2Relevant academic research and scientific papers

Polyamide-6,6-based blocky copolyamides obtained by solid-state modification

Jeyakumar, Albert,Goossens, Han,Noordover, Bart,Prusty, Manoranjan,Scheibitz, Matthias,Koning, Cor

, p. 5118 - 5129 (2013)

Copolyamides based on polyamide-6,6 (PA-6,6) were prepared by solid-state modification (SSM). Para- and meta-xylylenediamine were successfully incorporated into the aliphatic PA-6,6 backbone at 200 and 230 °C under an inert gas flow. In the initial stage of the SSM below the melting temperature of PA-6,6, a decrease of the molecular weight was observed due to chain scission, followed by a built up of the molecular weight and incorporation of the comonomer by postcondensation during the next stage. When the solid-state copolymerization was continued for a sufficiently long time, the starting PA-6,6 molecular weight was regained. The incorporation of the comonomer into the PA-6,6 main chain was confirmed by size exclusion chromatography (SEC) with ultraviolet detection, which showed the presence of aromatic moieties in the final high-molecular weight SSM product. The occurrence of the transamidation reaction was also proven by 1H nuclear magnetic resonance (NMR) spectroscopy. As the transamidation was limited to the amorphous phase, this SSM resulted in a nonrandom overall structure of the PA copolymer as shown by the degree of randomness determined using 13C NMR spectroscopy. The thermal properties of the SSM products were compared with melt-synthesized copolyamides of similar chemical composition. The higher melting and higher crystallization temperatures of the solid state-modified copolyamides confirmed their nonrandom, block-like chemical microstructure, whereas the melt-synthesized copolyamides were random. Copyright

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