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1,3,5-Triaminobenzene trihydrochloride, with the molecular formula C6H9N3 ? 3HCl, is a white crystalline solid that is soluble in water. It is a salt formed by the reaction of 1,3,5-triaminobenzene with hydrochloric acid and has a melting point of approximately 240°C. 1,3,5-TRIAMINOBENZENE TRIHYDROCHLORIDE serves as a versatile reagent in organic synthesis and finds applications in various industries due to its unique properties.

638-09-5

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638-09-5 Usage

Uses

Used in Organic Synthesis:
1,3,5-Triaminobenzene trihydrochloride is used as a reagent in the synthesis of various organic compounds. Its trisubstituted amine structure makes it a valuable building block for the creation of complex organic molecules.
Used in Metalworking Fluids:
In the metalworking industry, 1,3,5-triaminobenzene trihydrochloride is used as a corrosion inhibitor. Its ability to prevent the corrosion of metal surfaces during manufacturing processes helps to extend the life of machinery and reduce maintenance costs.
Used in Dye Production:
1,3,5-Triaminobenzene trihydrochloride is utilized in the production of dyes. Its chemical structure allows for the creation of a wide range of colors, making it a valuable component in the dye industry.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 1,3,5-triaminobenzene trihydrochloride is used in the synthesis of various drugs. Its unique properties enable the development of new medications with potential therapeutic benefits.
Used in Polymer Production:
1,3,5-TRIAMINOBENZENE TRIHYDROCHLORIDE is also used in the production of polymers. Its ability to form stable bonds with other molecules contributes to the creation of polymers with specific properties, such as conductivity or resistance to certain conditions.
Used in Materials Science:
1,3,5-Triaminobenzene trihydrochloride has potential applications in the field of materials science, particularly in the synthesis of conductive polymers and coordination polymers. Its role in creating materials with unique electronic properties makes it an important component in the development of advanced materials for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 638-09-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 638-09:
(5*6)+(4*3)+(3*8)+(2*0)+(1*9)=75
75 % 10 = 5
So 638-09-5 is a valid CAS Registry Number.

638-09-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name benzene-1,3,5-triamine,trihydrochloride

1.2 Other means of identification

Product number -
Other names Benzene-1,3,5-triamine trihydrochloride

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:638-09-5 SDS

638-09-5Relevant academic research and scientific papers

Modular Construction of Porous Hydrogen-Bonded Molecular Materials from Melams

Khadivjam, Tinasadat,Che-Quang, Huy,Maris, Thierry,Ajoyan, Zvart,Howarth, Ashlee J.,Wuest, James D.

, p. 7026 - 7040 (2020)

Ordered materials with predictable structures and properties can be made by a modular approach, using molecules designed to interact with neighbors and hold them in predetermined positions. Incorporating 4,6-diamino-1,3,5-triazin-2-yl (DAT) groups in modules is an effective way to direct assembly because each DAT group can form multiple N?H???N hydrogen bonds according to established patterns. We have found that modules with high densities of N(DAT)2 groups can be made by base-induced double triazinylations of readily available amines. The resulting modules can form structures held together by remarkably large numbers of hydrogen bonds per molecule. Even simple modules with only 1–3 N(DAT)2 groups and fewer than 70 non-hydrogen atoms can crystallize to form highly open networks in which each molecule engages in over 20 N?H???N hydrogen bonds, and more than 70 % of the volume is available for accommodating guests. In favorable cases, guests can be removed to create rigorously porous crystalline solids analogous to zeolites and metal–organic frameworks.

Safer conditions for the Curtius rearrangement of 1,3,5- benzenetricarboxylic acid

Davis, Matthew C.

, p. 3519 - 3528 (2008/03/13)

A rapid method to prepare 1,3,5-triaminobenzene and its derivatives is the tris-Curtius rearrangment of 1,3,5-benzenetricarboxylic acid. The hazards associated with the acyl azide route are minimized by using 1,2-dichloroethane as solvent. A second method that avoids acyl azide preparation uses diphenylphosphoryl azide to yield the tricarbamate in one step. Copyright Taylor & Francis Group, LLC.

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