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4,4'-Diamino-3,3'-dimethyl diphenyl cyclohexane, also known as Hardener H, is an aliphatic diamine that serves as a high-performance hardening agent in the production of epoxy resins and adhesive products. This chemical compound is renowned for its versatility and its ability to significantly enhance the toughness, chemical resistance, mechanical, and thermal properties of epoxy-based materials. Its low viscosity and excellent curing properties make it a valuable ingredient in the formulation of high-quality composite materials and adhesives. Furthermore, its low color and low odor characteristics render it suitable for a wide range of manufacturing processes.

6442-08-6

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6442-08-6 Usage

Uses

Used in Epoxy Resin Industry:
4,4'-Diamino-3,3'-dimethyl diphenyl cyclohexane is used as a curing agent for enhancing the toughness and chemical resistance of epoxy-based materials. Its application results in improved mechanical and thermal properties, which are crucial for the production of durable and reliable epoxy resins.
Used in Adhesive Products:
In the adhesive products industry, 4,4'-Diamino-3,3'-dimethyl diphenyl cyclohexane is utilized as a hardening agent to improve the bonding strength and durability of adhesive formulations, ensuring strong and long-lasting adhesion in various applications.
Used in Coatings Production:
4,4'-Diamino-3,3'-dimethyl diphenyl cyclohexane is employed as a key component in the production of coatings, where it contributes to the development of coatings with enhanced performance characteristics, such as increased toughness, chemical resistance, and thermal stability.
Used in Sealants Industry:
In the sealants industry, 4,4'-Diamino-3,3'-dimethyl diphenyl cyclohexane is used as a curing agent to improve the sealing performance and durability of sealant formulations, providing effective sealing solutions for various industrial applications.
Used in Composite Materials:
4,4'-Diamino-3,3'-dimethyl diphenyl cyclohexane is utilized in the production of composite materials to enhance their mechanical properties, making them suitable for applications requiring high strength and durability.
Used in Manufacturing Processes:
Due to its low color and low odor properties, 4,4'-Diamino-3,3'-dimethyl diphenyl cyclohexane is an ideal ingredient for various manufacturing processes where color and odor are critical factors for the final product quality.

Check Digit Verification of cas no

The CAS Registry Mumber 6442-08-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,4 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6442-08:
(6*6)+(5*4)+(4*4)+(3*2)+(2*0)+(1*8)=86
86 % 10 = 6
So 6442-08-6 is a valid CAS Registry Number.

6442-08-6SDS

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 4-[1-(4-amino-3-methylphenyl)cyclohexyl]-2-methylaniline

1.2 Other means of identification

Product number -
Other names 4,4'-Cyclohexylidenedi-o-toluidine

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:6442-08-6 SDS

6442-08-6Relevant academic research and scientific papers

Syntheses of biphenyl polyimides via nickel-catalyzed coupling polymerization of bis(chlorophthalimide)s

Gao, Changlu,Zhang, Suobo,Gao, Lianxun,Ding, Mengxian

, p. 5559 - 5565 (2007/10/03)

A facile method for the synthesis of biphenyl polyamides, which involves the nickel-catalyzed coupling of aromatic dichlorides containing imide structure in the presence of zinc and triphenylphosphine, has been developed. The polymerizations proceeded smoothly under mild conditions and produced biphenyl polyimides with inherent viscosities of 0.13-0.98 dL/g. The polymerizations of bis(4-chlorophthalimide)s with bulky side substituents gave high molecular weight polymers. Low molecular weight polymers from bis(4-chlorophthalimide)s containing rigid diamine moieties and bis(3-chlorophthalimide)s were obtained because of the formations of polymer precipitate and cyclic oligoimides, respectively. The effects of various factors, such as amount of catalyst, solvent volume, ligand, reaction temperature, and time, on the polymerization were studied. The random copolymerization of two bis(chlorophthalimide)s in varying proportions produced medium molecular weight material. The Tgs of prepared polyimides were observed at 245 - 311 °C, and the thermogravimetry of polymers showed 10% weight loss in nitrogen at 470-530 °C.

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