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3-Hydroxyanthranilic Acid - >97.0%, high purity , CAS No.548-93-6

In stock
Item Number
H157079
Grouped product items
SKU Size
Availability
Price Qty
H157079-250mg
250mg
3
$19.90
H157079-1g
1g
6
$25.90
H157079-5g
5g
2
$109.90
H157079-25g
25g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$529.90

Basic Description

Synonyms CCRIS 4427 | 3-Hydroxy-2-aminobenzoate | 3-Hydroxy-anthranilsaeure [German] | NSC 522891 | 3-HAA, 3-HANA | AI3-52837 | CHEBI:15793 | EN300-98786 | WLN: ZR BQ FVQ | HMS3373P15 | SY030553 | 1u1w | 3-hydroxyantranilic acid | DTXSID40203290 | ACon1_002137 | A
Specifications & Purity Moligand™, ≥97%
Shipped In Normal
Grade Moligand™
Product Description

3-Hydroxyanthranilic acid is an aminobenzoic acid commonly used as an intermediate in various chemical reactions.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Benzoic acids and derivatives
Intermediate Tree Nodes Not available
Direct Parent Hydroxybenzoic acid derivatives
Alternative Parents Aminobenzoic acids  Benzoic acids  o-Aminophenols  Aniline and substituted anilines  Benzoyl derivatives  1-hydroxy-2-unsubstituted benzenoids  1-hydroxy-4-unsubstituted benzenoids  Vinylogous amides  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Hydrocarbon derivatives  Organic oxides  Organooxygen compounds  Organopnictogen compounds  Primary amines  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Aminobenzoic acid - Aminobenzoic acid or derivatives - Hydroxybenzoic acid - Benzoic acid - O-aminophenol - Aminophenol - Benzoyl - Aniline or substituted anilines - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Vinylogous amide - Amino acid or derivatives - Amino acid - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organonitrogen compound - Hydrocarbon derivative - Amine - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Primary amine - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as hydroxybenzoic acid derivatives. These are compounds containing a hydroxybenzoic acid (or a derivative), which is a benzene ring bearing a carboxyl and a hydroxyl groups.
External Descriptors monohydroxybenzoic acid - aminobenzoic acid

Associated Targets(Human)

CASP6 Tchem Caspase-6 (1213 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CASP9 Tchem Caspase-9 (154 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CASP7 Tchem Caspase-7 (3146 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PDK1 Tchem Pyruvate dehydrogenase kinase isoform 1 (2021 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HEK293 (82097 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Jurkat (10389 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
POLK Tbio DNA polymerase kappa (8653 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
POLI Tchem DNA polymerase iota (116820 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CD28 Tbio T-cell-specific surface glycoprotein CD28 (1 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
G6PD Tchem Glucose-6-phosphate 1-dehydrogenase (778 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
IDH1 Tclin Isocitrate dehydrogenase [NADP] cytoplasmic (40980 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Mus musculus (284745 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
RAW264.7 (28094 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
dnaB Replicative DNA helicase (15 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Large T antigen (1457 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
recA Protein RecA (2211 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
G6PD-6PGL Glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase (1761 Activities)
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 488179486
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488179486
IUPAC Name 2-amino-3-hydroxybenzoic acid
INCHI InChI=1S/C7H7NO3/c8-6-4(7(10)11)2-1-3-5(6)9/h1-3,9H,8H2,(H,10,11)
InChIKey WJXSWCUQABXPFS-UHFFFAOYSA-N
Smiles C1=CC(=C(C(=C1)O)N)C(=O)O
Isomeric SMILES C1=CC(=C(C(=C1)O)N)C(=O)O
WGK Germany 3
RTECS DG2625000
Molecular Weight 153.14
Beilstein 14(3)1463
Reaxy-Rn 973356
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=973356&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.

14 results found

Lot Number Certificate Type Date Item
E2529190 Certificate of Analysis Jan 14, 2025 H157079
B2517349 Certificate of Analysis Jan 14, 2025 H157079
B2517353 Certificate of Analysis Jan 14, 2025 H157079
B2508314 Certificate of Analysis Jan 14, 2025 H157079
B2508328 Certificate of Analysis Jan 14, 2025 H157079
F2523087 Certificate of Analysis Jan 14, 2025 H157079
L2307115 Certificate of Analysis Dec 15, 2023 H157079
K1813152 Certificate of Analysis Sep 15, 2022 H157079
G2213582 Certificate of Analysis Jul 16, 2022 H157079
H2231469 Certificate of Analysis Jun 22, 2022 H157079
D2419020 Certificate of Analysis Jun 22, 2022 H157079
H2231471 Certificate of Analysis Jun 22, 2022 H157079
G2321028 Certificate of Analysis Jun 22, 2022 H157079
H2231464 Certificate of Analysis Jun 22, 2022 H157079

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Chemical and Physical Properties

Solubility Slightly soluble in water; Soluble in Ether,Chloroform,Alcohol
Melt Point(°C) 240°C
Molecular Weight 153.140 g/mol
XLogP3 0.900
Hydrogen Bond Donor Count 3
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 1
Exact Mass 153.043 Da
Monoisotopic Mass 153.043 Da
Topological Polar Surface Area 83.600 Ų
Heavy Atom Count 11
Formal Charge 0
Complexity 160.000
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

Solution Calculators

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