2-Chloro-4-nitrophenol - ≥97% , CAS No.619-08-9

CAS: 619-08-9 Cat. No.: C104236 Molecular Weight: 173.55 Beilstein Registry Number: 6240 EC Number: 210-578-8
AVAILABLE TO ORDER
GRADE & PURITY ≥97%
Synonyms
BRN 2046372 | Nitrofurgin | AC-10766 | AM20040873 | SY006700 | EN300-18946 | AKOS000119853 | UNII-Y2V03M9UL8 | 2-chloro-4nitrophenol | 2-CHLORO-4-NITROPHENOL | 2-chloro4-nitro-phenol | AH-034/32465052 | Y2V03M9UL8 | DTXSID0060694 | Phenol, chloro-4-nitro-
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
C104236-1g
2
$9.90
5g
C104236-5g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$10.90
25g
C104236-25g
1

$13.90

$20.90
Save $7.00 (33.49%)
100g
C104236-100g
1

$21.90

$32.90
Save $11.00 (33.43%)
500g
C104236-500g
1

$102.90

$154.90
Save $52.00 (33.57%)
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Why this grade

≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
BRN 2046372 | Nitrofurgin | AC-10766 | AM20040873 | SY006700 | EN300-18946 | AKOS000119853 | UNII-Y2V03M9UL8 | 2-chloro-4nitrophenol | 2-CHLORO-4-NITROPHENOL | 2-chloro4-nitro-phenol | AH-034/32465052 | Y2V03M9UL8 | DTXSID0060694 | Phenol, chloro-4-nitro-
Specifications & Purity
≥97%
Storage
Room temperature
Shipped In
Normal
Action Type
INHIBITOR
Purity
≥97%
Names and Identifiers
Pubchem Sid504752257
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504752257
Canonical SmilesC1=CC(=C(C=C1[N+](=O)[O-])Cl)O
IUPAC Name2-chloro-4-nitrophenol
InChIKeyBOFRXDMCQRTGII-UHFFFAOYSA-N
INCHI1S/C6H4ClNO3/c7-5-3-4(8(10)11)1-2-6(5)9/h1-3,9H
Isomeric SMILES C1=CC(=C(C=C1[N+](=O)[O-])Cl)O
WGK Germany 3
RTECS SK5075000
UN Number 2811
Molecular Weight 173.55
Beilstein 6240
Reaxy-Rn 2046372
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2046372&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassPhenols
SubclassNitrophenols
Intermediate Tree Nodes Not available
Direct ParentNitrophenols
Alternative Parents Nitrobenzenes  O-chlorophenols  Nitroaromatic compounds  Chlorobenzenes  1-hydroxy-2-unsubstituted benzenoids  Aryl chlorides  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Organopnictogen compounds  Organooxygen compounds  Organonitrogen compounds  Organochlorides  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Nitrophenol - Nitrobenzene - Nitroaromatic compound - 2-halophenol - 2-chlorophenol - 1-hydroxy-2-unsubstituted benzenoid - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Organic nitro compound - C-nitro compound - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organochloride - Organohalogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as nitrophenols. These are compounds containing a nitrophenol moiety, which consists of a benzene ring bearing both a hydroxyl group and a nitro group on two different ring carbon atoms.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Mechanisms of Action
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.

13 results found

Lot NumberCertificate TypeDateItem
D2622062Certificate of AnalysisMay 06, 2026 C104236
D2617059Certificate of AnalysisApr 23, 2026 C104236
E2614030Certificate of AnalysisApr 23, 2026 C104236
A1928035Certificate of AnalysisMar 20, 2026 C104236
J2023144Certificate of AnalysisFeb 05, 2026 C104236
D2017081Certificate of AnalysisAug 15, 2025 C104236
L2129107Certificate of AnalysisOct 09, 2023 C104236
L2129108Certificate of AnalysisOct 09, 2023 C104236
L2129165Certificate of AnalysisOct 09, 2023 C104236
L2129167Certificate of AnalysisOct 09, 2023 C104236
K2129327Certificate of AnalysisSep 15, 2023 C104236
D2327050Certificate of AnalysisNov 13, 2021 C104236
E2323019Certificate of AnalysisNov 13, 2021 C104236

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Chemical and Physical Properties
SolubilitySlightly Soluble in water.
SensitivityMoisture sensitive.
Melt Point(°C)106-112°C
Molecular Weight173.550 g/mol
XLogP32.300
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count0
Exact Mass172.988 Da
Monoisotopic Mass172.988 Da
Topological Polar Surface Area66.100 Ų
Heavy Atom Count11
Formal Charge0
Complexity158.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Jiayue Dong, Peizeng Yang, Jing Chen, Yuefei Ji, Junhe Lu.  (2022)  Nitrophenolic byproducts formation during sulfate radical oxidation and their fate in simulated drinking water treatment processes.  WATER RESEARCH,      [PMID:36088770] [10.1016/j.watres.2022.119054]
2. Feng Li, Qi-Le Li, Lei Hu, Hong-Yu Zhu, Wen-Juan Wang, Fen-Ying Kong, Heng-Ye Li, Zhong-Xia Wang, Wei Wang.  (2021)  Ratiometric detection of p-nitrophenol and its derivatives using a dual-emissive neuron cell-like carbonized probe based on a π⋯π stacking quenching mechanism.  ANALYST,  146  (14): (4566-4575).  [PMID:34152330] [10.1039/D1AN00891A]
3. Fu Yang, Jin Wang, Shuying Gao, Shijian Zhou, Yan Kong.  (2020)  Record-high catalytic hydrogenated activity in nitroarenes reduction derived from in-situ nascent active metals enabled by constructing bimetallic phosphate.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2020.110873]
4. Yanhong Zheng, Zeyu Song, Muwei Huang, Cancan Li, Chunke Nong, Tinghao Jiang, Zhanji Li, Zhongsheng Yi.  (2025)  Elucidating thyroid hormone transport proteins disruption by nitrophenols through computational and spectroscopic analysis.  BIOPHYSICAL CHEMISTRY,      [PMID:39987709] [10.1016/j.bpc.2025.107415]
Solution Calculators
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