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2,3,4,6-Tetrachlorophenol Standard - 2000ug/ml in Methanol, high purity , CAS No.58-90-2
Basic Description
Synonyms
2,3,4,6-TETRACHLOROPHENOL | 58-90-2 | Dowicide 6 | 2,4,5,6-Tetrachlorophenol | Phenol, 2,3,4,6-tetrachloro- | 1-Hydroxy-2,3,4,6-tetrachlorobenzene | DTXSID9021716 | NSC-2428 | 2,4,5,6-Tetrachlorophenol-13C6 | 2442S914FX | DTXCID201716 | Chlorophenols | NSC 2428 | RCRA waste number
Specifications & Purity
2000ug/ml in Methanol
Storage Temp
Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description
Phenols Single Compound Standards US EPA Methods:604,627,8270,1311
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Phenols
Subclass
Halophenols
Intermediate Tree Nodes
Chlorophenols
Direct Parent
P-chlorophenols
Alternative Parents
O-chlorophenols M-chlorophenols Chlorobenzenes Aryl chlorides Organooxygen compounds Organochlorides Hydrocarbon derivatives
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
4-chlorophenol - 2-chlorophenol - 3-chlorophenol - Halobenzene - Chlorobenzene - Monocyclic benzene moiety - Aryl halide - Aryl chloride - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organochloride - Organohalogen compound - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as p-chlorophenols. These are chlorophenols carrying a iodine at the C4 position of the benzene ring.
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
2,3,4,6-tetrachlorophenol
INCHI
InChI=1S/C6H2Cl4O/c7-2-1-3(8)6(11)5(10)4(2)9/h1,11H
InChIKey
VGVRPFIJEJYOFN-UHFFFAOYSA-N
Smiles
C1=C(C(=C(C(=C1Cl)Cl)Cl)O)Cl
Isomeric SMILES
C1=C(C(=C(C(=C1Cl)Cl)Cl)O)Cl
WGK Germany
1
PubChem CID
6028
UN Number
2811
Packing Group
I
Molecular Weight
231.89
Beilstein
779754
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Flash Point(°F)
11 °C
Flash Point(°C)
11°C
Boil Point(°C)
164°C
Melt Point(°C)
69-70°C
Molecular Weight
231.900 g/mol
XLogP3
4.500
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
0
Exact Mass
231.883 Da
Monoisotopic Mass
229.886 Da
Topological Polar Surface Area
20.200 Ų
Heavy Atom Count
11
Formal Charge
0
Complexity
143.000
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.
Ge Kun, Li Yonghui, Wu Qiyue, Gu Ying.
(2022)
Simultaneous and rapid detection of polychlorinated phenols in water samples by surface-enhanced Raman spectroscopy combined with principal component analysis. ANALYTICAL AND BIOANALYTICAL CHEMISTRY,
414
(7):
(2385-2395).
2.
Jingjing Hu, Sen Wang, Jiaqi Yu, Wenkai Nie, Jie Sun, Shaobin Wang.
(2021)
Duet Fe3C and FeNx Sites for H2O2 Generation and Activation toward Enhanced Electro-Fenton Performance in Wastewater Treatment. ENVIRONMENTAL SCIENCE & TECHNOLOGY,
55
(2):
(1260–1269).
3.
Yun Zhang, Shanshan Yin, Lingling Yu, Saijun Shangguan, Chencheng Song, Qin Li, Ke Chen, Jie Sun, Mei Li, Haobo Hou.
(2019)
Protocells self-assembled by hydroxyapatite nanoparticles: Highly efficient and selective enrichment of chlorophenols in an aqueous environment. CHEMOSPHERE,
233
(1).
4.
Chen-Xuan Li, Yun-Jie Wang, Chang-Bin Chen, Xian-Zhong Fu, Shuo Cui, Jia-Yuan Lu, Hou-Qi Liu, Wen-Wei Li.
(2019)
Interactions between chlorophenols and peroxymonosulfate: pH dependency and reaction pathways. SCIENCE OF THE TOTAL ENVIRONMENT,
664
(133).
5.
Xingru Hu, Chaohai Wang, Rui Luo, Chao Liu, Junwen Qi, Xiuyun Sun, Jinyou Shen, Weiqing Han, Lianjun Wang, Jiansheng Li.
(2019)
Double -shelled hollow ZnO/carbon nanocubes as an efficient solid-phase microextraction coating for the extraction of broad-spectrum pollutants. Nanoscale,
11
(6):
(2805-2811).
6.
Sheng-Dong Pan, Xiao-Hong Chen, Hao-Yu Shen, Xiao-Ping Li, Mei-Qiang Cai, Yong-Gang Zhao, Mi-Cong Jin.
(2016)
RETRACTED: Rapid and effective sample cleanup based on graphene oxide-encapsulated core–shell magnetic microspheres for determination of fifteen trace environmental phenols in seafood by liquid chromatography–tandem mass spectrometry. ANALYTICA CHIMICA ACTA,
919
(34).
7.
Yu Wang, Qian-Yuan Wu, Min-Yong Lee, Yu-Jia Nong, Wen-Long Wang, Jörg E. Drewes.
(2024)
Efficient Electrocatalytic Hydrodechlorination and Detoxification of Chlorophenols by Palladium–Palladium Oxide Heterostructure. ENVIRONMENTAL SCIENCE & TECHNOLOGY,
58
(46):
(20739-20750).
8.
Yu-Jia Nong, Qian-Yuan Wu, Yun-Peng Wu, Ju-Won Lee, Min-Yong Lee, Wen-Long Wang.
(2025)
Far-UVC (UV222) based photolysis, photooxidation, and photoreduction of chlorophenols using a KrCl-excimer lamp: Degradation, dechlorination, and detoxification. WATER RESEARCH,
268
(122560).
9.
Xingzhi Jin, Di Gao, Chunyan Zhang, Chen Chen, Yuyue Li, Hao Chen, Peng Cai, Jianwei Li, Xing Ding.
(2024)
Unveiling chlorine's role: How it shapes the formation and light-activated oxygen dynamics of chlorophenol-derived environmental persistent free radicals. JOURNAL OF HAZARDOUS MATERIALS,
480
(135870).
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9 Citations
B23271077