10325-89-0

Basic information

• Product Name: 2,5-Diaminobenzene-1,4-diol
• Synonyms: 2,5-Diamino-1,4-benzenediol;2,5-Diaminobenzene-1,4-diol
• CAS NO: 10325-89-0
• Molecular Formula: C₆H₈N₂O₂
• Molecular Weight: 140.14
• Mol File: 10325-89-0.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,5-Diaminobenzene-1,4-diol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Diaminobenzene-1,4-diol(10325-89-0)
• EPA Substance Registry System: 2,5-Diaminobenzene-1,4-diol(10325-89-0)

Safety Data

• Hazardous Substances Data: 10325-89-0(Hazardous Substances Data)

Usage

Type of compound

dihydroxybenzene derivative

Uses

production of hair dyes and colorant products, intermediate in the synthesis of dyes and pigments, formulation of photographic developers

Physical form

crystalline solid

Solubility

soluble in water

Industrial applications

wide range due to ability to react with various compounds to form colored products

Health hazard

recognized human health hazard, should be handled with care and proper safety measures.

Upstream product

• 1521-06-8 2,5-diaminocyclohexa-2,5-diene-1,4-dione 
• 21086-65-7 4,5-dimethoxy-1,2-benzoquinone 
• 3117-03-1 2,5-dimethoxyquinone 
• 120-80-9 benzene-1,2-diol 
• 57-68-1 sulfadimesine 
• 118-75-2 chloranil 
• 3908-48-3 2,5-diamino-3,6-dichloro-1,4-benzoquinone 

Downstream Products

• 1151760-14-3 2,6-bis(3,4,5-tridodecyloxyphenyl)benzo[1,2-d;4,5-d']bisoxazole 
• 267-94-7 benzo[1,2-d;4,5-d']bisoxazole 
• 783366-39-2 1,2-difluoro-4-oxo-4H-pyrido[3,2,1-kl]-8-(3'-hydroxy-4'-amino-(N-2-fluoro-4-nitrophenyl)-phenyl)-5-carboxylic acid 
• 783366-36-9 ethyl 2-(2',3',4',5'-tetrafluorobenzoyl)-3-(N-(4-hydroxy-2-aminophenoxazole))-prop-2-enoate 
• 783366-32-5 2-amino(t-butoxycarbonyl)-5-aminohydroquinone 

Relevant articles and documents

Degradation of sulfonamides in aqueous solution by membrane anodic Fenton treatment

Two agricultural antibiotics used heavily in agriculture, sulfamethazine and sulfadiazine, were degraded in an aqueous system by anodic Fenton treatment (AFT), an advanced oxidation technique that has been shown to be effective in degrading various pesticides but has not been applied to antibiotics. The effects of the H2O2/Fe2+ ratio, Fe2+ delivery rate, and initial contaminant concentration on the degradation of sulfamethazine by AR were determined. The optimal H2O 2/Fe2+ ratio was determined to be 10:1, and the optimal Fe2+ delivery rate was found to be between 38.9 and 54.4 μM min-1. Under these conditions, sulfamethazine was completely degraded within 10 min at a range of concentrations (18-250 μM)commonly found in manure lagoons, contaminated rivers, and groundwater. Using the same optimal conditions, the effect of pH on the degradation of sulfadiazine by AFT was analyzed, and 100 μM sulfadiazine was degraded within 6-8 min of treatment at a range of pH values (3.1-7.1) that could potentially be found in aquatic environments. Degradation products and pathways were proposed for both compounds, and it was inferred that AFT degradation products of sulfadiazine and sulfamethazine are unlikely to retain the bacteriostatic properties of their parent compounds. An aquatic toxicity test employing Lemna gibba confirmed that AFT removes the bacteriostatic properties of sulfamethazine and sulfadiazine during degradation.

Synthesis, characterization, spectral property, Hirshfeld surface analysis and TD/DFT calculations of 2, 6-disubstituted benzobisoxazoles

An effective and clean aerobic oxidative method for the synthesis of 2,6-disubstituted benzobisoxazole using the free radical catalysis was obtained. 2, 6-Di(pyridin-4-yl)-benzo[1,2-d:4,5-d']bisoxazole was synthesized and characterized by 1H an

PREPARATION OF BIS (AMINE-CONTAINING) BENZENEDIOLS

Bis (amine-containing) benzenediols are prepared by the hydrogenation and dehalogenation of bis (amine-contain-ing) dihalobenzoquinones using formic acid, formate salts or mixtures thereof in the presence of a noble metal catalyst. An example of a compoun