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3,3'-Dihydroxybenzidine - 98%, high purity , CAS No.2373-98-0
Basic Description
Synonyms
InChI=1/C12H12N2O2/c13-9-3-1-7(5-11(9)15)8-2-4-10(14)12(16)6-8/h1-6,15-16H,13-14H2 | 3,3'-dihydroxy-4,4'-diamino-bipheny | SY052119 | 3,3'-Dihydroxy-4,4'-diaminobiphenyl | 3,3'-Dihydroxy-4,4'-diamino-biphenyl | CCRIS 9225 | Q27285684 | ZGDMDBHLKNQPSD-UHFF
Specifications & Purity
≥98%
Storage Temp
Argon charged
Shipped In
Normal
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Biphenyls and derivatives
Intermediate Tree Nodes
Benzidines
Direct Parent
3,3'-disubstituted benzidines
Alternative Parents
o-Aminophenols Aniline and substituted anilines 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Primary amines Organopnictogen compounds Organooxygen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
3,3'-disubstituted benzidine - Aminophenol - O-aminophenol - Aniline or substituted anilines - Phenol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Organic nitrogen compound - Primary amine - Amine - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as 3,3'-disubstituted benzidines. These are organic compounds containing a benzidine skeleton, which is substituted only at the 3- and 3'-positions.
External Descriptors
Not available
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
IUPAC Name
2-amino-5-(4-amino-3-hydroxyphenyl)phenol
INCHI
InChI=1S/C12H12N2O2/c13-9-3-1-7(5-11(9)15)8-2-4-10(14)12(16)6-8/h1-6,15-16H,13-14H2
InChIKey
ZGDMDBHLKNQPSD-UHFFFAOYSA-N
Smiles
C1=CC(=C(C=C1C2=CC(=C(C=C2)N)O)O)N
Isomeric SMILES
C1=CC(=C(C=C1C2=CC(=C(C=C2)N)O)O)N
RTECS
DV4900000
Molecular Weight
216.24
Beilstein
13(2)502
Reaxy-Rn
2725972
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2725972&ln=
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Insoluble in water; Soluble in Dimethylformamide
Sensitivity
air sensitive
Melt Point(°C)
292°C
Molecular Weight
216.240 g/mol
XLogP3
1.500
Hydrogen Bond Donor Count
4
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
1
Exact Mass
216.09 Da
Monoisotopic Mass
216.09 Da
Topological Polar Surface Area
92.500 Ų
Heavy Atom Count
16
Formal Charge
0
Complexity
213.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
1.
Zenghui Xie, Yuling Hu, Jiana Lin, Gongke Li, Qisheng Zhong.
(2023)
Calix[4]arene-based covalent organic frameworks with host-guest recognition for selective adsorption of six per- and polyfluoroalkyl substances in food followed by UHPLC-MS/MS detection.
JOURNAL OF HAZARDOUS MATERIALS,
459
(132198).
2.
Lili Zhang, Xinghua Zhang, Xinghai Wei, Deqi Jing, Weiguo Su, Shouchun Zhang.
(2022)
Hydroxyl-functionalized block co-polyimide enables simultaneously improved toughness and strength of tetrafunctional epoxy resin.
COMPOSITES SCIENCE AND TECHNOLOGY,
230
(109787).
3.
Jinmin Wang, Limin Zhao, Bing Yan.
(2022)
Postsynthetic functionalization of covalent organic frameworks for dual channel fluorescence diagnosis of two indicators related to Parkinson's disease.
SENSORS AND ACTUATORS B-CHEMICAL,
355
(131297).
4.
Xiao Zhang, Qin Yang, Yunhe Lang, Xia Jiang, Peng Wu.
(2020)
Rationale of 3,3′,5,5′-Tetramethylbenzidine as the Chromogenic Substrate in Colorimetric Analysis.
ANALYTICAL CHEMISTRY,
92
(18):
(12400–12406).
5.
Zheng Hu, Yuhang Yang, Zhe Li, Qiuying Tao, Yinghong Huang, Xian Wang.
(2025)
Efficient enrichment and sensitive determination of endocrine disruptors in PPCPs by novel magnetic covalent organic framework extraction coupled with HPLC-MS/MS.
TALANTA,
287
(127667).
6.
Rusong Sang, Yezi Hu, Zewen Shen, Guixia Zhao, Junrong Yue, Xiubing Huang.
(2024)
Low-temperature synthesis of porous organic polymers with donor–acceptor structure and β-ketoenamine for photocatalytic oxidative coupling of amines.
Nanoscale,
16
(18):
(8931-8940).
7.
Chunyi Yu, Xujing Kong, Wenting Li, Boyu Li, Baorong Chen, Mengyao Gao, Susu Cai, Yun Wei.
(2025)
Magnetic molecularly imprinted polymers coupled with UPLC-MS/MS for simultaneous detection of 19 steroid hormones in human plasma.
JOURNAL OF CHROMATOGRAPHY A,
(465655).
8.
Manyan Qiu, Yueling Tian, Wenxuan Qu, Yu Ma, Feng Zhao, Yujun Jiang, Qianyu Zhao, Chaoxin Man.
(2025)
Postbiotic-biosynthesized silver nanoparticles anchored on covalent organic frameworks integrated into carboxymethyl chitosan-based film for enhancing antibacterial packaging.
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,
291
(139143).
9.
Chenglong Sun, Ying Han, Hongyu Guo, Rui Zhao, Youxing Liu, Zheng Lin, Zehao Xiao, Zongqiang Sun, Mingchuan Luo, Shaojun Guo.
(2025)
Proton Reservoir in Covalent Organic Framework Compensating Oxygen Reduction Reaction Enhances Hydrogen Peroxide Photosynthesis.
ADVANCED MATERIALS,
(2502990).
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