2-Nitro-1-naphthol - ≥98% , CAS No.607-24-9

CAS: 607-24-9 Cat. No.: N139066 Summenformel: C10H7O3N Molekulargewicht: 189.17 EG-Nummer: 210-131-7
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GRADE & PURITY ≥98%
Synonyms
2-Nitro-1-naphthol | 1-Naphthol, 2-nitro- | 2-Nitro-naphthalen-1-ol | 2-nitronaphthalen-1-ol | DTXSID70209508 | MUCCHGOWMZTLHK-UHFFFAOYSA- | 2-Nitronaphth-1-ol;2-Nitronaphthalen-1-ol | MFCD00003956 | nitronaphthol | NSC43140 | NSC-43140 | SKE3TA8XGH | AKO
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
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Size
Deutschland (EU)
USA*
Price
Qty
1g
N139066-1g
Auf Bestellung · 8–12 Wochen
8,59€
5g
N139066-5g
—
4 Auf Lager
16,40€
25g
N139066-25g
—
3 Auf Lager
46,77€
100g
N139066-100g
Auf Bestellung · 8–12 Wochen
86,69€
Enter a quantity for the sizes you want to add.
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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.

Übersicht

It was employed as substrate for use in an amperometric 3-electrode system for the determination of alkaline phosphatase,it also used in electrochemical immunoassays, the preparation of di-(2-nitro-1-naphthyl) hydrogen phosphate and 1-(2′-methyl-3′-indenyl)-2-naphthylamine and -2-naphthol (axially chiral ligands)

Specifications

Synonyme
2-Nitro-1-naphthol | 1-Naphthol, 2-nitro- | 2-Nitro-naphthalen-1-ol | 2-nitronaphthalen-1-ol | DTXSID70209508 | MUCCHGOWMZTLHK-UHFFFAOYSA- | 2-Nitronaphth-1-ol;2-Nitronaphthalen-1-ol | MFCD00003956 | nitronaphthol | NSC43140 | NSC-43140 | SKE3TA8XGH | AKO
Spezifikationen & Reinheit
≥98%
Storage
Store at 2-8°C,Argon charged
Verschickt in
Wet ice
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Reinheit
≥98%
Namen und Kennungen
Pubchem Sid528757476
Kanonisches LächelnC1=CC=C2C(=C1)C=CC(=C2O)[N+](=O)[O-]
IUPAC Name2-nitronaphthalen-1-ol
InChIKeyMUCCHGOWMZTLHK-UHFFFAOYSA-N
INCHI1S/C10H7NO3/c12-10-8-4-2-1-3-7(8)5-6-9(10)11(13)14/h1-6,12H
Isomere SMILES C1=CC=C2C(=C1)C=CC(=C2O)[N+](=O)[O-]
WGK Deutschland 3
Molekulargewicht 189.17
Reaxy-Rn 2050016
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2050016&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
KlasseNaphthalenes
SubclassNitronaphthalenes
Intermediate Tree Nodes Not available
Direct ParentNitronaphthalenes
Alternative Parents Naphthols and derivatives  Nitroaromatic compounds  1-hydroxy-4-unsubstituted benzenoids  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Organopnictogen compounds  Organooxygen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents 2-nitronaphthalene - 1-naphthol - Nitroaromatic compound - 1-hydroxy-4-unsubstituted benzenoid - C-nitro compound - Organic nitro compound - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Aromatic homopolycyclic compound
BeschreibungThis 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-Struktur
Interaktives chemisches Strukturmodell





Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
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.

4 results found

Lot NumberCertificate TypeDatumArtikel
K2528452Certificate of AnalysisSep 22, 2025 N139066
L2510632Certificate of AnalysisSep 22, 2025 N139066
L2510639Certificate of AnalysisSep 22, 2025 N139066
L2510641Certificate of AnalysisSep 22, 2025 N139066
Chemische und physikalische Eigenschaften
Molekulargewicht189.170 g/mol
XLogP32.900
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
Referenzen
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]
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