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6-Heptyl-1,3,5-triazine-2,4-diamine is an organic compound with the molecular formula C10H17N5. It is a derivative of the triazine family, characterized by a six-membered heterocyclic ring containing three nitrogen atoms and three carbon atoms. The compound features a heptyl (seven-carbon) alkyl chain attached to the 6th position of the triazine ring, and two amino groups (-NH2) at the 2nd and 4th positions. This chemical is known for its potential applications in various fields, such as pharmaceuticals, agrochemicals, and dyes, due to its unique structure and reactivity. However, it is essential to handle 6-Heptyl-1,3,5-triazine-2,4-diamine with care, as it may have potential health and environmental risks.

6025-08-7

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6025-08-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6025-08-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,2 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6025-08:
(6*6)+(5*0)+(4*2)+(3*5)+(2*0)+(1*8)=67
67 % 10 = 7
So 6025-08-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H19N5/c1-2-3-4-5-6-7-8-13-9(11)15-10(12)14-8/h2-7H2,1H3,(H4,11,12,13,14,15)

6025-08-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-heptyl-1,3,5-triazine-2,4-diamine

1.2 Other means of identification

Product number -
Other names 6-heptyl-[1,3,5]triazine-2,4-diyldiamine

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:6025-08-7 SDS

6025-08-7Downstream Products

6025-08-7Relevant academic research and scientific papers

Triple hydrogen bonds direct crystal engineering of metal-assembled complexes: The effect of a novel organic-inorganic module on supramolecular structure

Adachi, Keiichi,Sugiyama, Yuichi,Yoneda, Ko,Yamada, Koichi,Nozaki, Koichi,Fuyuhiro, Akira,Kawata, Satoshi

, p. 6616 - 6628 (2005)

Novel triply hydrogen bonded suprastructures based on [M-(tdpd) 2(L)2]2- (H2tdpd= 1,4,5,6-tetrahydro-5,6-dioxo-2,3-pyrazinedicarbonitrile, L = solvent) and melamine-analogous cations have been synthesized and characterized. The use of anions containing two AAA sets from [M-(tdpd)2(L)2] 2 together with cations containing one ODD set (A = hydrogen-bond acceptor, D = hydrogen-bond donor) leads to the formation of complementary triply hydrogen bonded modules in the solid state. In all cases, the building module is further extended via additional hydrogen-bonding in teractions to produce a tape, and tapes are assembled into sheets. These results show that a hydrogen-bonded module consisting of different kinds of building blocks, one of which is a metal complex that includes hydrogen-bond acceptor sites and the other is a hydrogen-bond donor molecule, will be attractive for constructing metal-containing supramolecular systems by the self-assembly technique.

Colorant compositions and processes

-

, (2008/06/13)

A process for making solid colored particles by preparing a reaction solution in water comprising formaldehyde, urea, a cyclic polyamine functional triazine compound, and acid. A dye can be incorporated into the reaction solution if a color other than white is desired. Particles are formed having an average particle size between 1 and 70 microns without the need to resort to crushing to break up agglomerates. Particles made by this process provide excellent color and are easily washable from a substrate when incorporated into a washable formulation. Additionally, it has been found that the incorporation of colored microcapsules of average size of 1-70 microns where the color is located primarily on or in the shell of the microcapsule also provides excellent washable compositions when incorporated into a washable formulation.

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