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4-Amino-2-chlorophenol - >98.0%(GC), high purity , CAS No.3964-52-1

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4-Amino-2-chlorophenol - >98.0%(GC), high purity , CAS No.3964-52-1

COA

Grade & Purity:

≥98%(GC)

Cas Number: 3964-52-1
Molecular Weight: 143.57
MDL number: MFCD00128891
PubChem CID: 77578
PubChem SID: 488185427

In stock

Item Number

A151243

Grouped product items
SKU	Size	Availability	Price
A151243-1g	1g	5	$9.90
A151243-5g	5g	4	$22.90
A151243-25g	25g	1	$66.90
A151243-100g	100g	1	$239.90

View related series

Oxygenated compounds (806) phenol (506)

Basic Description

Synonyms	FT-0611752 \| InChI=1/C6H6ClNO/c7-5-3-4(8)1-2-6(5)9/h1-3,9H,8H \| Eburnamonine (-) \| M-CHLORO-P-HYDROXYANILINE \| A6624 \| BB 0246799 \| 2-chloro-p-aminophenol \| 4-Amino-2-chlorophenol; (3-Chloro-4-hydroxyphenyl)amine; 2-Chloro-4-aminophenol; 2-Chloro-p-aminop
Specifications & Purity	≥98%(GC)
Storage Temp	Store at 2-8°C,Argon charged
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	4-Amino-2-chlorophenol (4A2CP) is a chlorinated aniline. Nephrotoxic potential of 4-amino-2-chlorophenol and its comparison with 4-aminophenol, 4-amino-2-chlorophenol, 4-amino-3-chlorophenol and 4-amino-2,6-dichlorophenol using isolated renal cortical cells from male Fischer 344 rats has been investigated. -Amino-2-chlorophenol may be used in the synthesis of the following compounds: . N-(3-chloro-4-hydroxyphenyl)-N′,N′-dimethylurea . 1,4-diketo-3-((4-[N-(3-chloro-4-hydroxyphenyl)amino]sulfonyl)phenyl)-6-phenylpyrrolo[3,4-c]pyrrole, a novel fluorescent pH-i

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Phenols
    - Subclass Halophenols
      - Level5 Chlorophenols
        Level6 O-chlorophenols

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Phenols
Subclass	Halophenols
Intermediate Tree Nodes	Chlorophenols
Direct Parent	O-chlorophenols
Alternative Parents	p-Aminophenols Aniline and substituted anilines Chlorobenzenes 1-hydroxy-2-unsubstituted benzenoids Aryl chlorides Primary amines Organopnictogen compounds Organooxygen compounds Organochlorides Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Aminophenol - P-aminophenol - Aniline or substituted anilines - 2-chlorophenol - 1-hydroxy-2-unsubstituted benzenoid - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Amine - Organochloride - Organohalogen compound - Organonitrogen compound - Organooxygen compound - Primary amine - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as o-chlorophenols. These are chlorophenols carrying a iodine at the C2 position of the benzene ring.
External Descriptors	Not available
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. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

CA2 Tclin Carbonic anhydrase II (17698 Activities)

Discover Target: CA2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA1 Tclin Carbonic anhydrase I (13240 Activities)

Discover Target: CA1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	488185427
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488185427
IUPAC Name	4-amino-2-chlorophenol
INCHI	InChI=1S/C6H6ClNO/c7-5-3-4(8)1-2-6(5)9/h1-3,9H,8H2
InChIKey	ZYZQSCWSPFLAFM-UHFFFAOYSA-N
Smiles	C1=CC(=C(C=C1N)Cl)O
Isomeric SMILES	C1=CC(=C(C=C1N)Cl)O
WGK Germany	3
Molecular Weight	143.57
Reaxy-Rn	2802560
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2802560&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

15 results found

Lot Number	Certificate Type	Date	Item
H1731043	Certificate of Analysis	Apr 02, 2025	A151243
E2415176	Certificate of Analysis	Apr 15, 2024	A151243
E2415177	Certificate of Analysis	Apr 15, 2024	A151243
E2415178	Certificate of Analysis	Apr 15, 2024	A151243
E2415179	Certificate of Analysis	Apr 15, 2024	A151243
G2301021	Certificate of Analysis	Jun 25, 2023	A151243
G2301020	Certificate of Analysis	Jun 25, 2023	A151243
G2301018	Certificate of Analysis	Jun 25, 2023	A151243
G2301019	Certificate of Analysis	Jun 25, 2023	A151243
G2301022	Certificate of Analysis	Jun 25, 2023	A151243
G2301028	Certificate of Analysis	Jun 25, 2023	A151243
G2303456	Certificate of Analysis	Jun 25, 2023	A151243
C2306869	Certificate of Analysis	Mar 15, 2023	A151243
G2213005	Certificate of Analysis	Jul 16, 2022	A151243
G2213012	Certificate of Analysis	Jul 16, 2022	A151243

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Chemical and Physical Properties

Solubility	DMSO (Slightly), Methanol (Slightly)
Sensitivity	air sensitive & heat sensitive
Melt Point(°C)	150-153°C
Molecular Weight	143.570 g/mol
XLogP3	1.800
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	0
Exact Mass	143.014 Da
Monoisotopic Mass	143.014 Da
Topological Polar Surface Area	46.300 Å²
Heavy Atom Count	9
Formal Charge	0
Complexity	99.100
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

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