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N,N'-dipropylbutane-1,4-diamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23346-57-8

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23346-57-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23346-57-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,3,4 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23346-57:
(7*2)+(6*3)+(5*3)+(4*4)+(3*6)+(2*5)+(1*7)=98
98 % 10 = 8
So 23346-57-8 is a valid CAS Registry Number.

23346-57-8SDS

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 N,N'-dipropylbutane-1,4-diamine

1.2 Other means of identification

Product number -
Other names N,N'-Dipropyl-1,4-butanediamine

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:23346-57-8 SDS

23346-57-8Downstream Products

23346-57-8Relevant academic research and scientific papers

Highly reactive, liquid diacrylamides via synergistic combination of spatially arranged curing moieties

Maier, Maximilian,Schmidt, Magnus S.,Ringwald, Markus,Fik, Christoph P.

, p. 372 - 383 (2017/03/14)

Six polymerizable N,N′-diacylamides containing spatially arranged N-acryl, N-allyl and/or N-alkyl groups were prepared via two-step syntheses and characterized by 1H/13C NMR-spectra, refractive index (RI) and viscosity measurements. Photo DSC measurements on activated samples provided reactivity parameters ΔHp, Rp,max and tmax, while FTIR spectra before and after curing elucidated the underlying polymerization mechanism. Mechanical testing of the obtained polymers exhibited gradual differences in network densities, depending on the intramolecular arrangement and number of functional groups. Overall, a general building principle for highly reactive, liquid diacrylamides via synergistic combination of optimally arranged functional groups could be identified. The highest possible level of intramolecular synergism was found for low viscous N,N′-diacryloyl-N,N′-diallyl-1,4-but-2-enediamine.

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