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3,5-Dichlorosalicylic Acid - >98.0%(HPLC), high purity , CAS No.320-72-9

1 Citations

COA

Grade & Purity:

≥98%(HPLC)

Cas Number: 320-72-9
Molecular Weight: 207.01
Beilstein Registry Number: 10(3)169
MDL number: MFCD00002442
PubChem CID: 9445
PubChem SID: 488180980

In stock

Item Number

D154845

Grouped product items
SKU	Size	Availability	Price
D154845-5g	5g	3	$9.90
D154845-25g	25g	8	$30.90
D154845-100g	100g	2	$94.90
D154845-500g	500g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$361.90

View related series

carboxylic acid (2098) Non heterocyclic block (8163)

Basic Description

Synonyms	C2U \| Salicylic acid, 3,5-dichloro- \| NSC 30109 \| PS-4183 \| STK299334 \| AI3-22601 \| WLN: QVR BQ CG EG \| NSC30109 \| NSC-30109 \| Q27285414 \| UNII-O6PXR32G3V \| 3,5-Dichlorosalicylic acid, 97% \| J-018623 \| BDBM26269 \| EINECS 206-281-8 \| InChI=1/C7H4Cl2O3/c8-3
Specifications & Purity	≥98%(HPLC)
Shipped In	Normal
Product Description	3,5-Dichlorosalicylic acid is a bio-active drug and its interaction with a model transport protein bovine serum albumin has been investigated. It is a potential inhibitor of human 20α-hydroxysteroid dehydrogenase.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Benzene and substituted derivatives
    - Subclass Benzoic acids and derivatives
      - Level5 Benzoic acids
        Level6 Dichlorobenzoic acids

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Benzene and substituted derivatives
Subclass	Benzoic acids and derivatives
Intermediate Tree Nodes	Benzoic acids
Direct Parent	Dichlorobenzoic acids
Alternative Parents	Salicylic acids Halobenzoic acids 3-halobenzoic acids P-chlorophenols O-chlorophenols Dichlorobenzenes Benzoyl derivatives Aryl chlorides Vinylogous acids Monocarboxylic acids and derivatives Carboxylic acids Organooxygen compounds Organochlorides Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	3,5-dichlorobenzoic acid - Hydroxybenzoic acid - Salicylic acid or derivatives - Salicylic acid - Halobenzoic acid - 3-halobenzoic acid - Halobenzoic acid or derivatives - 3-halobenzoic acid or derivatives - Benzoyl - 1,3-dichlorobenzene - 4-halophenol - 2-halophenol - 2-chlorophenol - 4-chlorophenol - Halobenzene - Chlorobenzene - Phenol - Aryl halide - Aryl chloride - Vinylogous acid - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Carboxylic acid - Organohalogen compound - Organic oxide - Organic oxygen compound - Organochloride - Organooxygen compound - Hydrocarbon derivative - Aromatic homomonocyclic compound
Description	This 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	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)

AKR1C2 Tchem Aldo-keto reductase family 1 member C2 (2 Activities)

Discover Target: AKR1C2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

AKR1C1 Tchem Aldo-keto reductase family 1 member C1 (9 Activities)

Discover Target: AKR1C1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

AKR1A1 Tchem Aldehyde reductase (91 Activities)

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

AKR1C3 Tchem Aldo-keto-reductase family 1 member C3 (1414 Activities)

Discover Target: AKR1C3

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

AKR1C4 Tchem Aldo-keto reductase family 1 member C4 (224 Activities)

Discover Target: AKR1C4

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

AKR1C2 Tchem Aldo-keto reductase family 1 member C2 (639 Activities)

Discover Target: AKR1C2

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	488180980
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488180980
IUPAC Name	3,5-dichloro-2-hydroxybenzoic acid
INCHI	InChI=1S/C7H4Cl2O3/c8-3-1-4(7(11)12)6(10)5(9)2-3/h1-2,10H,(H,11,12)
InChIKey	CNJGWCQEGROXEE-UHFFFAOYSA-N
Smiles	C1=C(C=C(C(=C1C(=O)O)O)Cl)Cl
Isomeric SMILES	C1=C(C=C(C(=C1C(=O)O)O)Cl)Cl
WGK Germany	3
RTECS	VO2450000
Molecular Weight	207.01
Beilstein	10(3)169
Reaxy-Rn	2210803
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2210803&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.

3 results found

Lot Number	Certificate Type	Date	Item
F2328055	Certificate of Analysis	Sep 19, 2022	D154845
K1819033	Certificate of Analysis	Sep 19, 2022	D154845
D23061122	Certificate of Analysis	Sep 19, 2022	D154845

Chemical and Physical Properties

Melt Point(°C)	227 °C
Molecular Weight	207.010 g/mol
XLogP3	2.900
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	1
Exact Mass	205.954 Da
Monoisotopic Mass	205.954 Da
Topological Polar Surface Area	57.500 Å²
Heavy Atom Count	12
Formal Charge	0
Complexity	185.000
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

How to Cite Aladdin Scientific Products?

1. Yumin He, Pengcheng Li, Haohao Ren, Xi Zhang, Xiulian Chen, Yonggang Yan. (2021) The fabrication and neutron shielding property of polyphenylene sulfide containing salicylic acid/Gd2O3 composites. HIGH PERFORMANCE POLYMERS,

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