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N-(2,4-dinitrophenyl)hexane-1,6-diamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40299-04-5

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40299-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40299-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,9 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 40299-04:
(7*4)+(6*0)+(5*2)+(4*9)+(3*9)+(2*0)+(1*4)=105
105 % 10 = 5
So 40299-04-5 is a valid CAS Registry Number.

40299-04-5SDS

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'-(2,4-dinitrophenyl)hexane-1,6-diamine

1.2 Other means of identification

Product number -
Other names N-(6-aminohexyl)-2,4-dinitroaniline

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:40299-04-5 SDS

40299-04-5Downstream Products

40299-04-5Relevant academic research and scientific papers

EPOXY-CONTAINING POLY(ESTER AMIDES) AND METHODS OF USE

-

Page/Page column 48-49, (2010/11/30)

The invention provides aliphatic epoxy-containing PEA polymer compositions with film-forming properties. The aliphatic epoxy di-acids used in the invention PEA compositions include non-toxic fatty aliphatic epoxy homologs. A second, C-protected L-lysine-based monomer can be introduced into the polymer to provide additional chain flexibility. The invention PEA polymer compositions are useful for delivery of bioactive agents when administered internally or used in the manufacture of implantable medical devices. Biodegradable hydrogels can be made using the invention epoxy-containing PEAs.

Chromatographic approach to the measurement of the interstrand distance for some chiral bonded phases

Pirkle, William H.,Readnour, Robin S.

, p. 16 - 20 (2007/10/02)

A series of homologous N,N′-bis(2,4-dinitrophenyl)-α,ω-diaminoalkanes (bis-DNP's) was chromatographed at various temperatures on π-basic chiral stationary phases derived from N-(2-naphthyl)alanine in order to determine the enthalpy and entropy of adsorption. The number of methylene groups in the bis-DNP's influences the ability of the terminal π-acidic groups to interact simultaneously with neighboring strands of stationary phase, a process termed "bridging". When the number of methylene groups is optimal for bridging, the enthalpy of adsorption is most exothermic. The length of the bis-derivative required for optimal bridging is related to the interstrand distance. Optimal bridging occurs for the bis-DNP's having five methylene groups regardless of the extent of surface coverage of the silica for the surface coverage range investigated. This suggests that the strands are not randomly spaced on the silica, with interstrand distance being influenced only by surface coverage, but are instead clustered, the clusters having similar distributions of interstrand distances. Adsorption is more exothermic for phases of high surface coverages than for low. If Interstrand spacing is independent of surface coverage but surface coverage affects the enthalpy of adsorption, then surface coverage must influence the cluster size, which then influences the average extent of solvation of a strand of bonded phase.

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