2-Amino-3-hydroxypyridine - ≥97% , CAS No.16867-03-1

CAS: 16867-03-1 Cat. No.: A101241 Molecular Weight: 110.11 Beilstein Registry Number: 109868 EC Number: 240-886-8
AVAILABLE TO ORDER
GRADE & PURITY ≥97%
Synonyms
2-amino-pyridin-3-ol | 2-Aminopyridin-3-ol | BMTSZVZQNMNPCT-UHFFFAOYSA- | NSC136806 | NSC-136806 | P16526 | BBL009590 | InChI=1/C5H6N2O/c6-5-4(8)2-1-3-7-5/h1-3,8H,(H2,6,7) | F2158-1509 | W-107900 | AKOS000119509 | 3-HYDROXY-2-AMINOPYRIDINE | AI3-61061 | E
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5g
A101241-5g
5
$12.90
25g
A101241-25g
4
$26.90
100g
A101241-100g
3
$36.90
250g
A101241-250g
1
$91.90
500g
A101241-500g
1
$181.90
Enter a quantity for the sizes you want to add.
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Why this grade

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

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

product description:

2-Amino-3-hydroxypyridine forms complexes with number of transition metals. It inhibits the corrosion of aluminium and copper in acidic solutions. It undergoes condensation with 2-hydroxy-1-naphthaldehyde and 2-hydroxybenzaldehyde to form Schiffs bases. It is useful in the preparation of clinical anti-inflammatory analgesics.


application:

2-Amino-3-hydroxypyridine was used as reagent in reaction of dimethyl acetylenedicarboxylate and triphenylphosphine to yield functionalized coumarins and 1,4-oxazines.

Specifications

Synonyms
2-amino-pyridin-3-ol | 2-Aminopyridin-3-ol | BMTSZVZQNMNPCT-UHFFFAOYSA- | NSC136806 | NSC-136806 | P16526 | BBL009590 | InChI=1/C5H6N2O/c6-5-4(8)2-1-3-7-5/h1-3, 8H, (H2, 6, 7) | F2158-1509 | W-107900 | AKOS000119509 | 3-HYDROXY-2-AMINOPYRIDINE | AI3-61061 | E
Specifications & Purity
≥97%
Storage
Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥97%
Names and Identifiers
Pubchem Sid488183072
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488183072
Canonical SmilesC1=CC(=C(N=C1)N)O
IUPAC Name2-aminopyridin-3-ol
InChIKeyBMTSZVZQNMNPCT-UHFFFAOYSA-N
INCHI1S/C5H6N2O/c6-5-4(8)2-1-3-7-5/h1-3,8H,(H2,6,7)
Isomeric SMILES C1=CC(=C(N=C1)N)O
WGK Germany 3
UN Number UN 2811
Packing Group III
Molecular Weight 110.11
Beilstein 109868
Reaxy-Rn 109868
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=109868&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
SuperclassOrganoheterocyclic compounds
ClassPyridines and derivatives
SubclassAminopyridines and derivatives
Intermediate Tree Nodes Not available
Direct ParentAminopyridines and derivatives
Alternative Parents Hydroxypyridines  Imidolactams  Heteroaromatic compounds  Azacyclic compounds  Primary amines  Organopnictogen compounds  Organooxygen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Hydroxypyridine - Aminopyridine - Imidolactam - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Amine - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as aminopyridines and derivatives. These are organic heterocyclic compounds containing an amino group attached to a pyridine ring.
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.

14 results found

Lot NumberCertificate TypeDateItem
H1820060Certificate of AnalysisMar 20, 2026 A101241
I2109029Certificate of AnalysisJun 09, 2025 A101241
I2109030Certificate of AnalysisJun 09, 2025 A101241
E2128420Certificate of AnalysisMar 04, 2025 A101241
K2418088Certificate of AnalysisJun 13, 2024 A101241
J2313039Certificate of AnalysisSep 15, 2023 A101241
J2313041Certificate of AnalysisSep 15, 2023 A101241
K2208026Certificate of AnalysisOct 25, 2022 A101241
K2208027Certificate of AnalysisOct 25, 2022 A101241
K2208028Certificate of AnalysisOct 25, 2022 A101241
K2208029Certificate of AnalysisOct 25, 2022 A101241
K2208030Certificate of AnalysisOct 25, 2022 A101241
B2321241Certificate of AnalysisAug 23, 2021 A101241
B2321015Certificate of AnalysisJun 16, 2021 A101241

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Chemical and Physical Properties
SolubilitySlightly soluble in water; soluble in methanol and ethanol
Sensitivityair&heat sensitive
Melt Point(°C)168-172°C
Molecular Weight110.110 g/mol
XLogP30.100
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count0
Exact Mass110.048 Da
Monoisotopic Mass110.048 Da
Topological Polar Surface Area59.100 Ų
Heavy Atom Count8
Formal Charge0
Complexity76.800
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. Wentao Chen, Kuo Su, Yuqiong Huang, Keith Gregory Brooks, Sachin Kinge, Bao Zhang, Yaqing Feng, Mohammad Khaja Nazeeruddin, Yi Zhang.  (2022)  Bifunctional additive 2-amino-3-hydroxypyridine for stable and high-efficiency tin–lead perovskite solar cells.  Journal of Materials Chemistry C,  11  (1): (151-160).  [PMID:] [10.1039/D2TC04000J]
Solution Calculators
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