2,4-Dichlorbenzoic acid - ≥98% , CAS No.50-84-0

CAS: 50-84-0 Cat. No.: D401393 Peso molecular: 191.01 Beilstein Registry Number: 1868192 Número EC: 200-067-8
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
AKOS000119754 | BB 0240623 | CCRIS 9472 | Benzoic acid, 2,4-dichloro- | FT-0610044 | NCGC00091214-02 | BRN 1868192
Storage
Room temperature
Shipped In
Normal
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Size
Estado
Price
Qty
5g
D401393-5g
2
9,90US$
25g
D401393-25g
1
10,90US$
100g
D401393-100g
1

29,90US$

44,90US$
Guardar 15,00 US$ (33.41%)
500g
D401393-500g
1

65,90US$

98,90US$
Guardar 33,00 US$ (33.37%)
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Why this grade

≥98% 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.

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Literature proof

Cited in 9 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

2,4-Dichlorobenzoic acid is the degradation product of chlorfenvinphos in water treated by photo-fenton driven by solar irradiation.
Application:

2,4-Dichlorobenzoic acid was used in solid-phase extraction and gas chromatographic determination of polar acidic herbicides in surface water.2,4-Dichlorobenzoic acid was used as reagent during the synthesis of pyrimido[2′,1′:2,3]thiazolo[4,5-b]quinoxaline derivatives. 2,4-Dichlorobenzoic acid was used as starting reagent during the synthesis of 1-(substituted)-1,4-dihydro-6-nitro-4-oxo-7-(sub-secondary amino)-quinoline-3-carboxylic acids.

Specifications

Sinónimos
AKOS000119754 | BB 0240623 | CCRIS 9472 | Benzoic acid, 2, 4-dichloro- | FT-0610044 | NCGC00091214-02 | BRN 1868192
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Sonrisas canónicasC1=CC(=C(C=C1Cl)Cl)C(=O)O
IUPAC Name2,4-dichlorobenzoic acid
InChIKeyATCRIUVQKHMXSH-UHFFFAOYSA-N
INCHI1S/C7H4Cl2O2/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3H,(H,10,11)
Isómeros SMILES C1=CC(=C(C=C1Cl)Cl)C(=O)O
WGK Alemania 3
RTECS DG6650000
Peso molecular 191.01
Beilstein 1868192
Reaxy-Rn 1868192
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1868192&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
ClaseBenzene and substituted derivatives
SubclassBenzoic acids and derivatives
Intermediate Tree Nodes Benzoic acids
Direct ParentDichlorobenzoic acids
Alternative Parents Halobenzoic acids  4-halobenzoic acids  2-halobenzoic acids  Dichlorobenzenes  Benzoyl derivatives  1-carboxy-2-haloaromatic compounds  Aryl chlorides  Vinylogous halides  Monocarboxylic acids and derivatives  Organooxygen compounds  Organochlorides  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents 2,4-dichlorobenzoic acid - Halobenzoic acid - 4-halobenzoic acid - 2-halobenzoic acid - Halobenzoic acid or derivatives - 4-halobenzoic acid or derivatives - 2-halobenzoic acid or derivatives - Benzoyl - 1,3-dichlorobenzene - 1-carboxy-2-haloaromatic compound - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Vinylogous halide - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organochloride - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as dichlorobenzoic acids. These are benzoic acids having two chlorine atoms attached to the carboxylated benzene ring.
External Descriptors dichlorobenzene - chlorobenzoic acid
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CASP1 Tchem Caspase-1 (6235 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

9 results found

Lot NumberCertificate TypeFechaArticulo
C2630068Certificate of AnalysisDec 14, 2024 D401393
L2427256Certificate of AnalysisDec 14, 2024 D401393
L2427257Certificate of AnalysisDec 14, 2024 D401393
L2427258Certificate of AnalysisDec 14, 2024 D401393
L2427259Certificate of AnalysisDec 14, 2024 D401393
L2427261Certificate of AnalysisDec 14, 2024 D401393
L2427262Certificate of AnalysisDec 14, 2024 D401393
L2431108Certificate of AnalysisDec 14, 2024 D401393
L2431109Certificate of AnalysisDec 14, 2024 D401393
Propiedades químicas y físicas
SolubilidadSoluble in ethanol (100 mg/ml), water (0.48 mg/ml), alcohol, ether, and acetone.
Punto de ebullición (°C)200°C
Punto de fusión (°C)160-164°C
Peso molecular191.010 g/mol
XLogP32.800
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass189.959 Da
Monoisotopic Mass189.959 Da
Topological Polar Surface Area37.300 Ų
Heavy Atom Count11
Formal Charge0
Complexity161.000
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
Referencias
1. Wei Wang, Zhijuan Wang, Kai Li, Yuxin Liu, Delong Xie, Shaoyun Shan, Liang He, Yi Mei.  (2021)  Enhanced adsorption of aqueous chlorinated aromatic compounds by nitrogen auto-doped biochar produced through pyrolysis of rubber-seed shell.  ENVIRONMENTAL TECHNOLOGY,      [PMID:34516358] [10.1080/09593330.2021.1980829]
2. Jiasheng Zhou, Zimo Lou, Zheni Wang, Chuchen Zhou, Cheng Li, Shams Ali Baig, Xinhua Xu.  (2021)  Electrocatalytic dechlorination of 2,4-DCBA using CTAB functionalized Pd/GAC movable granular catalyst: Role of adsorption in catalysis.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2021.128758]
3. Nadeem Muhammad, Dandan Guo, Yun Zhang, Azeem Intisar, Qamar Subhani, Muhammad Abdul Qadir, Hairong Cui.  (2019)  Online clean-up setup for the determination of non-fluorescent acidic pharmaceutical drugs in complex biological samples.  JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES,      [PMID:31437773] [10.1016/j.jchromb.2019.06.035]
4. Zimo Lou, Jiang Xu, Jiasheng Zhou, Kunlun Yang, Zhen Cao, Yizhou Li, Yuanli Liu, Liping Lou, Xinhua Xu.  (2019)  Insight into atomic H* generation, H2 evolution, and cathode potential of MnO2 induced Pd/Ni foam cathode for electrocatalytic hydrodechlorination.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2019.05.171]
5. Jiasheng Zhou, Zimo Lou, Jiang Xu, Xiaoxin Zhou, Kunlun Yang, Xiaoyu Gao, Yilin Zhang, Xinhua Xu.  (2018)  Enhanced electrocatalytic dechlorination by dispersed and moveable activated carbon supported palladium catalyst.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2018.10.098]
6. Zimo Lou, Jiasheng Zhou, Mei Sun, Jiang Xu, Kunlun Yang, Dan Lv, Yaping Zhao, Xinhua Xu.  (2018)  MnO2 enhances electrocatalytic hydrodechlorination by Pd/Ni foam electrodes and reduces Pd needs.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2018.07.057]
7. Meng Liu, Chuming Yin, Peng Chen, Mingtao Zhang, Sean Parkin, Panpan Zhou, Tonglei Li, Faquan Yu, Sihui Long.  (2017)  sp2CH⋯Cl hydrogen bond in the conformational polymorphism of 4-chloro-phenylanthranilic acid.  CRYSTENGCOMM,  19  (30): (4345-4354).  [PMID:] [10.1039/C7CE00772H]
8. Fengping Liu, Aiming Zhong, Qin Xu, Hongen Cao, Xiaoya Hu.  (2016)  Inhibition of 2,4-Dichlorophenoxyacetic Acid to Catalase Immobilized on Hierarchical Porous Calcium Phosphate: Kinetic Aspect and Electrochemical Biosensor Construction.  Journal of Physical Chemistry C,      [PMID:] [10.1021/acs.jpcc.5b12559]
9. Yaxuan Peng, Meiyan Wang.  (2025)  MnO2-Supported Pd Nanocatalyst for Efficient Electrochemical Reduction of 2,4-Dichlorobenzoic Acid.  Clean Technologies,  (4): (102).  [PMID:] [10.3390/cleantechnol7040102]
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