291765-93-0

Basic information

• Product Name: 1,2-BENZENE-D4-DIAMINE
• Synonyms: 1,2-BENZENE-D4-DIAMINE;1,2-Phenylenediamine-3,4,5,6-d4
• CAS NO: 291765-93-0
• Molecular Formula: C₆H₈N₂
• Molecular Weight: 112.17
• Mol File: 291765-93-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2-BENZENE-D4-DIAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-BENZENE-D4-DIAMINE(291765-93-0)
• EPA Substance Registry System: 1,2-BENZENE-D4-DIAMINE(291765-93-0)

Safety Data

• Hazardous Substances Data: 291765-93-0(Hazardous Substances Data)

Usage

Uses

Used in the Production of High-Performance Polymers:
1,2-Benzene-d4-diamine is used as a key precursor in the synthesis of polybenzimidazole fiber, a high-performance thermoplastic polymer. This fiber is valued for its exceptional thermal stability and chemical resistance, making it suitable for various applications in demanding environments.
Used in the Synthesis of Dyes:
1,2-Benzene-d4-diamine is utilized as an intermediate in the production of dyes, contributing to the development of colorants with specific properties for various industries, such as textiles, printing, and cosmetics.
Used in Pharmaceutical Synthesis:
As an intermediate in the synthesis of pharmaceuticals, 1,2-Benzene-d4-diamine plays a crucial role in the development of new drugs and active pharmaceutical ingredients, potentially leading to advancements in healthcare and medicine.
Used in Organic Compounds Synthesis:
1,2-Benzene-d4-diamine is employed as an intermediate in the synthesis of various organic compounds, enabling the creation of a wide range of chemical products with diverse applications across different industries.

Upstream product

• 95-54-5 1,2-diamino-benzene 

Downstream Products

• 1176802-04-2 2,3-dihydro(4,5,6,7-D4)-1H-1,3-benzodiazol-2-one 
• 291765-95-2 methyl 2-aminobenzimidazolecarbamate-4,5,6,7-2H4 

Relevant articles and documents

Synthesis of deuterium labelled benomyl and carbendazim residue standards

Three environmental degradation products of benomyl possessing tetradeutero-ring substitutions were synthesized for use in quantitative analysis of trace residues. The common precursor, 1,2-phenylenediamine, was exhaustively deuterated upon heating in aci

Microwave mediated hydrogen deuterium exchange: A rapid synthesis of 2H-substituted benzimidazole

Deuterium aromatic substituted compounds were prepared by microwave irradiation of the parent unlabeled compounds in the presence of deuterium oxide and deuterium chloride. The percentage of deuterium incorporation was investigated under various reaction

Efficient and selective Pt/C-catalyzed H-D exchange reaction of aromatic rings

An effective and applicable deuteration method for aromatic rings using Pt/C-D2O-H2 system was established. Especially, phenol was fully deuterated even at room temperature, and other electron-rich aromatic nuclei were efficiently deuterated under mild conditions. The scope and limitations of the presence method and its application to the synthesis of deuterium-labeled biologically active compounds and deuterium-labeled building blocks for practical multi-gram scale syntheses are reported. 2008 The Chemical Society of Japan.

Aromatic ring favorable and efficient H-D exchange reaction catalyzed by Pt/C

An effective and applicable Pt/C-catalyzed deuteration method of aromatic rings using D2O as a deuterium source under hydrogen atmosphere was developed. Five percent Pt/C would lead to quite effective H-D exchange results on the aromatic ring systems. The reaction is general for a variety of aromatic compounds including biologically active compounds.