1009314-88-8

Basic information

• Product Name: (4-aminobenzene-1,3-diyl)dimethanol
• Synonyms: (4-aminobenzene-1,3-diyl)dimethanol;(4-amino-1,3-phenylene)dimethanol;(4-aminobezene-1,3-diyl)dimethanol;[4-amino-3-(hydroxymethyl)phenyl]methanol
• CAS NO: 1009314-88-8
• Molecular Formula: C₈H₁₁NO₂
• Molecular Weight: 153.17844
• Mol File: 1009314-88-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (4-aminobenzene-1,3-diyl)dimethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (4-aminobenzene-1,3-diyl)dimethanol(1009314-88-8)
• EPA Substance Registry System: (4-aminobenzene-1,3-diyl)dimethanol(1009314-88-8)

Safety Data

• Hazardous Substances Data: 1009314-88-8(Hazardous Substances Data)

Usage

General Description

(4-aminobenzene-1,3-diyl)dimethanol is a chemical compound with the molecular formula C8H11NO2. It is a diol, meaning it has two hydroxyl functional groups. (4-aminobenzene-1,3-diyl)dimethanol is commonly used in the production of various polymers and plastics, particularly as a cross-linking agent to improve the mechanical and thermal properties of the materials. It is also utilized in the synthesis of pharmaceuticals and as an intermediate in the manufacture of dyes, pigments, and other organic compounds. Additionally, (4-aminobenzene-1,3-diyl)dimethanol can also be employed as a building block in the production of specialty chemicals and as a reagent in organic chemical reactions. Overall, this compound has numerous industrial applications due to its versatile properties and chemical reactivity.

Upstream product

• 50-00-0 formaldehyd 
• 62-53-3 aniline 
• 1253261-36-7 2,4-bishydroxymethyl nitrobenzene 
• 1055310-33-2 C₂₀H₃₉NO₂Si₂ 

Downstream Products

• 1055310-34-3 C₂₄H₂₉NO₂Si 
• 1353003-37-8 C₃₇H₄₀N₂O₁₉ 

Relevant articles and documents

Synthesis and characterization of metal-incorporated aniline formaldehyde resin modified by amino acid for antimicrobial applications

Advances in metal incorporated resins are now an active field of research. To develop resin having better antimicrobial and thermal activity, a series of metal-chelated resins have been synthesized by the condensation of (4-aminobenzene-1,3-diyl)dimethanol with 2,6-diaminohexanoic acid in alkaline medium and then this polymeric ligand further reacts with transition metal ions forming various coordination polymers. (4-Aminobenzene-1,3-diyl)dimethanol was initially prepared by the reaction of aniline and formaldehyde in 1 : 2 molar ratio in alkaline medium. The analytical data reveal that the polymer metal complexes of Mn(II), Co(II), and Ni(II) are coordinated with two water molecules, which are further supported by FTIR spectra and TGA data. Comparative analyses of the polymer metal complexes in thermal curves show better thermal stability than the polymeric ligand. Since these resins are relatively stable at high temperatures, they can be used for medical and biomaterial applications requiring thermal sterilization, solvent-resist coating materials because of their insoluble nature, and antifouling coating materials owing to antimicrobial activity in Eelds such as life-saving medical devices and the bottoms of ships.

The azaquinone-methide elimination: Comparison study of 1,6- and 1,4-eliminations under physiological conditions

The azaquinone-methide elimination is a powerful and efficient reaction useful for disassembly of spacers in prodrug systems. We and others have used the spacer-technique to develop dendritic and polymeric self-immolative molecular systems that can disass