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N,N'-DIETHYL-6-HYDRAZINO-[1,3,5]TRIAZINE-2,4-DIAMINE, commonly referred to as DETDA, is an organic compound characterized by the chemical formula C8H20N6. It functions as a polyurethane curing agent, playing a pivotal role in the production of polyurethane-based materials such as coatings, adhesives, and elastomers. Renowned for its high performance and durability, DETDA is favored across various industries for its low viscosity, rapid curing time, and superior mechanical properties. Moreover, it is recognized for its safety when handled correctly and its compliance with environmental standards.

10421-98-4

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10421-98-4 Usage

Uses

Used in Automotive Industry:
DETDA is utilized as a curing agent for polyurethane coatings and adhesives, enhancing the durability and performance of automotive parts and components. Its fast curing time and excellent mechanical properties contribute to improved manufacturing efficiency and product quality.
Used in Construction Industry:
In the construction sector, DETDA serves as a key component in polyurethane-based materials for various applications, including insulation, sealing, and coating. Its high performance and durability ensure the longevity and reliability of construction materials.
Used in Industrial Applications:
DETDA is employed as a curing agent in the production of industrial-grade polyurethane coatings, adhesives, and elastomers. Its low viscosity and fast curing time facilitate efficient manufacturing processes, while its excellent mechanical properties ensure the robustness of the final products.
Used in Manufacturing Processes:
DETDA is used as a curing agent in various manufacturing processes to produce high-quality polyurethane materials. Its desirable properties, such as low viscosity and rapid curing time, make it a popular choice for creating coatings, adhesives, and elastomers with superior performance and durability.

Check Digit Verification of cas no

The CAS Registry Mumber 10421-98-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,2 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10421-98:
(7*1)+(6*0)+(5*4)+(4*2)+(3*1)+(2*9)+(1*8)=64
64 % 10 = 4
So 10421-98-4 is a valid CAS Registry Number.

10421-98-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-N,4-N-diethyl-6-hydrazinyl-1,3,5-triazine-2,4-diamine

1.2 Other means of identification

Product number -
Other names HMS1782E14

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:10421-98-4 SDS

10421-98-4Upstream product

10421-98-4Relevant academic research and scientific papers

Cardioprotective effect of novel sulphonamides-1,3,5-triazine conjugates against ischaemic–reperfusion injury via selective inhibition of MMP-9

Zheng, Xiao-Zhu,Zhou, Jia-Li,Ye, Jing,Guo, Pei-Pei,Lin, Chun-Shui

, p. 756 - 765 (2016)

Diseases affecting cardiovascular system are ranked as a top most cause of morbidity and mortality. Herein, a novel class sulphonamides-1,3,5-triazine conjugates have been synthesized and tested for inhibitory activity against MMP-2 and MMP-9. The results of the study showed that these molecules efficiently inhibit MMP-9 than MMP-2, revealing compound 8e as the most potent inhibitor (IC50?=?2.34?±?0.56?nm). Due to involvement of MMP-9 in many cardiovascular diseases, particularly in myocardial ischaemia (MI), compound 8e was further subjected for the determination of the protective effect on isoproterenol (ISO)-induced myocardial injury in rats.

Synthesis of imidazolinones, azetidinones and formazans from hydrazino-s-triazines as potential antimicrobial agents

Joshi, Nailesh,Bapodra, Atul,Parekh, Hansa

, p. 662 - 665 (2007/10/02)

2,4-Bis(ethylamino)-6-hydrazino-s-triazine (1) on treatment with 4-arylidene-2-phenyl-5-oxazolinone gives 4-arylidene-1--2-phenyl-5-oxo-2-imidazolines (2a-j).Also, compound 1 when refluxed with aromatic aldehydes yield the corresponding hydrazones (3a-j) which on reaction with chloroacetyl chloride and Et3N in dioxane afford 4-aryl-1--3-chloro-2-azetidinones (4a-j).The hydrazones (3a-j) also react with sulphanilamides furnishing 2,4-bis(ethylamino)-6--s-triazines (5a-j).Compounds 2d-q, 2i, 3a-c, 3e-f, 4a-g and 4i exhibit highest antimicrobial activity against the various strains of bacteria and fungi.

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