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3-Aminophenol - analytical standard,99%, high purity , CAS No.591-27-5

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Item Number
A108482
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A108482-1g
1g
5
$55.90
A108482-5g
5g
Available within 8-12 weeks(?)
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$239.90
A108482-25g
25g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$836.90
A108482-100g
100g
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Production requires sourcing of materials. We appreciate your patience and understanding.
$2,855.90
A108482-500g
500g
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Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$9,995.90

Basic Description

Synonyms 3-Aminophenol | 591-27-5 | M-AMINOPHENOL | 3-Hydroxyaniline | m-Hydroxyaniline | Phenol, 3-amino- | 3-Amino-1-hydroxybenzene | m-Hydroxyaminobenzene | Fouramine EG | Futramine EG | 1-Amino-3-hydroxybenzene | Fourrine EG | 3-amino-phenol | Pelagol EG | Tertral EG | Furro EG | Renal EG | Ur
Specifications & Purity analytical standard, ≥99%
Storage Temp Protected from light
Shipped In Normal
Grade analytical standard

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Aniline and substituted anilines
Intermediate Tree Nodes Not available
Direct Parent Aniline and substituted anilines
Alternative Parents m-Aminophenols  1-hydroxy-4-unsubstituted benzenoids  1-hydroxy-2-unsubstituted benzenoids  Primary amines  Organopnictogen compounds  Organooxygen compounds  Hydrocarbon derivatives  
Molecular Framework Aromatic homomonocyclic compounds
Substituents M-aminophenol - Aniline or substituted anilines - Aminophenol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Amine - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as aniline and substituted anilines. These are organic compounds containing an aminobenzene moiety.
External Descriptors aminophenol

Associated Targets(Human)

CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CA14 Tclin Carbonic anhydrase XIV (1305 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NR1H4 Tclin Bile acid receptor FXR (6228 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CA12 Tclin Carbonic anhydrase XII (6231 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CA9 Tclin Carbonic anhydrase IX (8255 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
GMNN Tbio Geminin (128009 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
RUNX1 Tbio Runt-related transcription factor 1/Core-binding factor subunit beta (7867 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Ca7 Carbonic anhydrase VII (3 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Bacillus subtilis (32866 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Poliovirus 1 (1274 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
L1210 (27553 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
TGR Thioredoxin glutathione reductase (28579 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 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

IUPAC Name 3-aminophenol
INCHI InChI=1S/C6H7NO/c7-5-2-1-3-6(8)4-5/h1-4,8H,7H2
InChIKey CWLKGDAVCFYWJK-UHFFFAOYSA-N
Smiles C1=CC(=CC(=C1)O)N
Isomeric SMILES C1=CC(=CC(=C1)O)N
WGK Germany 2
RTECS SJ4900000
UN Number 2512
Packing Group III
Molecular Weight 109.13
Beilstein 636059
Reaxy-Rn 636059
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=636059&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.

6 results found

Lot Number Certificate Type Date Item
K2425004 Certificate of Analysis Dec 04, 2023 A108482
K2321324 Certificate of Analysis Dec 04, 2023 A108482
E2112021 Certificate of Analysis Feb 10, 2023 A108482
D1919048 Certificate of Analysis Nov 11, 2022 A108482
H2321088 Certificate of Analysis Nov 11, 2022 A108482
I2206029 Certificate of Analysis Sep 09, 2022 A108482

Chemical and Physical Properties

Solubility Slightly soluble in water, soluble in alcohol and ether.
Sensitivity Light sensitive.
Flash Point(°C) 155℃
Boil Point(°C) 164 °C/11 mmHg
Melt Point(°C) 123℃
Molecular Weight 109.130 g/mol
XLogP3 0.200
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 0
Exact Mass 109.053 Da
Monoisotopic Mass 109.053 Da
Topological Polar Surface Area 46.300 Ų
Heavy Atom Count 8
Formal Charge 0
Complexity 74.900
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

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