4-Nitro-1-naphthol - ≥98% , CAS No.605-62-9

CAS: 605-62-9 Cat. No.: N122905 Molecular Weight: 189.17 EC Number: 611-992-5
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
1-Naphthalenol, 4-nitro- | J-013785 | 4-nitronaphthol | N0672 | SY029584 | HY-W015239 | EN300-72349 | BDBM50425036 | SCHEMBL589663 | Z1147461131 | AM20040822 | 4-nitronaphthalen-1-ol;1-Hydroxy-4-nitronaphthalene | 4-nitro-1-hydroxynaphthalene | A832781 |
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
N122905-1g
1

$10.90

$16.90
Save $6.00 (35.50%)
5g
N122905-5g
3

$33.90

$50.90
Save $17.00 (33.40%)
25g
N122905-25g
2

$143.90

$215.90
Save $72.00 (33.35%)
100g
N122905-100g
2

$568.90

$853.90
Save $285.00 (33.38%)
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🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.

📋

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.

Specifications

Synonyms
1-Naphthalenol, 4-nitro- | J-013785 | 4-nitronaphthol | N0672 | SY029584 | HY-W015239 | EN300-72349 | BDBM50425036 | SCHEMBL589663 | Z1147461131 | AM20040822 | 4-nitronaphthalen-1-ol;1-Hydroxy-4-nitronaphthalene | 4-nitro-1-hydroxynaphthalene | A832781 |
Specifications & Purity
≥98%
Storage
Store at 2-8°C, Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥98%
Names and Identifiers
Pubchem Sid504758523
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504758523
Canonical SmilesC1=CC=C2C(=C1)C(=CC=C2O)[N+](=O)[O-]
IUPAC Name4-nitronaphthalen-1-ol
InChIKeyAUIRNGLMBHIITH-UHFFFAOYSA-N
INCHI1S/C10H7NO3/c12-10-6-5-9(11(13)14)7-3-1-2-4-8(7)10/h1-6,12H
Isomeric SMILES C1=CC=C2C(=C1)C(=CC=C2O)[N+](=O)[O-]
Molecular Weight 189.17
Reaxy-Rn 1959672
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1959672&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
ClassNaphthalenes
SubclassNitronaphthalenes
Intermediate Tree Nodes Not available
Direct ParentNitronaphthalenes
Alternative Parents Naphthols and derivatives  Nitroaromatic compounds  1-hydroxy-2-unsubstituted benzenoids  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Organooxygen compounds  Organonitrogen compounds  Organic salts  Organic oxides  Hydrocarbon derivatives  Organic cations  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents 1-nitronaphthalene - 1-naphthol - Nitroaromatic compound - 1-hydroxy-2-unsubstituted benzenoid - Phenol - C-nitro compound - Organic nitro compound - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organic oxygen compound - Organic salt - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic cation - Aromatic homopolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as nitronaphthalenes. These are polycyclic aromatic compounds containing a naphthalene moiety substituted by one or more nitro groups.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
CTSB Tchem Cathepsin B (3822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EP300 Tchem Histone acetyltransferase p300 (1259 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KAT2B Tchem Histone acetyltransferase PCAF (884 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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.

8 results found

Lot NumberCertificate TypeDateItem
A2627131Certificate of AnalysisFeb 04, 2026 N122905
H2514083Certificate of AnalysisAug 22, 2025 N122905
I2104397Certificate of AnalysisJun 19, 2024 N122905
I2104398Certificate of AnalysisJun 19, 2024 N122905
I2104399Certificate of AnalysisJun 19, 2024 N122905
I2106023Certificate of AnalysisJun 19, 2024 N122905
L2405139Certificate of AnalysisJun 19, 2024 N122905
L2413013Certificate of AnalysisJun 19, 2024 N122905
Chemical and Physical Properties
SensitivityAir sensitive
Melt Point(°C)167°C
Molecular Weight189.170 g/mol
XLogP33.100
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count0
Exact Mass189.043 Da
Monoisotopic Mass189.043 Da
Topological Polar Surface Area66.100 Ų
Heavy Atom Count14
Formal Charge0
Complexity226.000
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
References
1. Jiayue Dong, Peizeng Yang, Deyang Kong, Yiqiang Song, Junhe Lu.  (2024)  Formation of nitrated naphthalene in the sulfate radical oxidation process in the presence of nitrite.  WATER RESEARCH,      [PMID:38574612] [10.1016/j.watres.2024.121546]
Solution Calculators
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