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2,3-diaminonaphthalene

CAS No.
771-97-1
Chemical Name:
2,3-diaminonaphthalene
Synonyms
Naphthalene-2,3-diamine;DAN;2,3-DIAMINONAPHTHALENE;2,3-NAPHTHALENEDIAMINE;DAND1;JACS-771-97-1;NAPHTHALENEDIAMINE;TIMTEC-BB SBB000127;2,3-DiaminonaphthaL;2,3-Diaminonapthalene
CBNumber:
CB8101895
Molecular Formula:
C10H10N2
Molecular Weight:
158.2
MDL Number:
MFCD00004116
MOL File:
771-97-1.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-24 14:58:21
Product description Number Pack Size Price
2,3-Diaminonaphthalene BioReagent, suitable for fluorescence, ≥98.0% (HPLC) 88461 25mg $58.2
2,3-Diaminonaphthalene BioReagent, suitable for fluorescence, ≥98.0% (HPLC) 88461 100mg $93.9
2,3-Diaminonaphthalene >98.0%(T) D1045 1g $133
2,3-Diaminonaphthalene >98.0%(T) D1045 5g $298
2,3-Diaminonaphthalene ≥98% 36265 100mg $30
More product size

2,3-diaminonaphthalene Properties

Melting point 197-203 °C
Boiling point 273.29°C (rough estimate)
Density 1.0968
refractive index 1.6392 (estimate)
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility pyridine: soluble50mg/mL
form Crystalline Powder
pka 5.36±0.10(Predicted)
color Green-brown to brown
Water Solubility Slightly soluble in water. Soluble in pyridine, dimethylsulfoxide, dimethyformamide, dil.hydrochloric acid, ethanol, ether and hot methanol.
BRN 2206394
Stability Stable. Combustible. Incompatible with strong oxidizing agents.
InChI InChI=1S/C10H10N2/c11-9-5-7-3-1-2-4-8(7)6-10(9)12/h1-6H,11-12H2
InChIKey XTBLDMQMUSHDEN-UHFFFAOYSA-N
SMILES C1=C2C(C=CC=C2)=CC(N)=C1N
CAS DataBase Reference 771-97-1(CAS DataBase Reference)
FDA UNII 2BNZ6BRS87
EPA Substance Registry System 2,3-Naphthalenediamine (771-97-1)
UNSPSC Code 12171500
NACRES NA.47

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS08
Signal word  Danger
Hazard statements  H302-H315-H319-H335-H350
Precautionary statements  P201-P202-P301+P312-P302+P352-P305+P351+P338-P308+P313
target organs Respiratory system
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xn,T
Risk Statements  22-36/37/38-45
Safety Statements  26-45-53
RIDADR  2811
WGK Germany  3
8-10-23
TSCA  TSCA listed
HS Code  29215900
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
NFPA 704
1
2 0

2,3-diaminonaphthalene price More Price(43)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 88461 2,3-Diaminonaphthalene BioReagent, suitable for fluorescence, ≥98.0% (HPLC) 771-97-1 25mg $58.2 2026-04-30 Buy
Sigma-Aldrich 88461 2,3-Diaminonaphthalene BioReagent, suitable for fluorescence, ≥98.0% (HPLC) 771-97-1 100mg $93.9 2026-04-30 Buy
TCI Chemical D1045 2,3-Diaminonaphthalene >98.0%(T) 771-97-1 1g $133 2026-04-30 Buy
TCI Chemical D1045 2,3-Diaminonaphthalene >98.0%(T) 771-97-1 5g $298 2026-04-30 Buy
Cayman Chemical 36265 2,3-Diaminonaphthalene ≥98% 771-97-1 100mg $30 2026-04-30 Buy
Product number Packaging Price Buy
88461 25mg $58.2 Buy
88461 100mg $93.9 Buy
D1045 1g $133 Buy
D1045 5g $298 Buy
36265 100mg $30 Buy

2,3-diaminonaphthalene Chemical Properties,Uses,Production

Description

2,3-Diaminonaphthalene is a highly selective colorimetric and fluorometric reagent for selenium detection and also used for the fluorometric determination of nitrite. It is also useful for detection of ketones and alpha-keto acids.
2,3-Diaminonaphthalene reacts with nitrosonium, which is formed from nitrite at low pH, to form the fluorescent dye 1 H-naphthotriazole. This method can be used to detect 10 nM to 10 uM of nitrite (NO2-) and is compatible with 96-well format.
Fluorometric probe for nitrite
Quantify 10 nM to 10 uM of nitrite
Yellow orange solid soluble in DMSO

Chemical Properties

colourless to white crystalline powder

Uses

2,3-Diaminonaphtaline (DAN) is used as a derivatisation-reagent for the determination of selenium at low detection limits.

Uses

In a reaction similar to that of DAF-FM , 2,3- diaminonaphthalene (D-7918) reacts with the nitrosonium cation that forms spontaneously from NO to form the fluorescent product 1H-naphthotriazole.Using 2,3-diaminonaphthalene, researchers have developed a rapid, quantitative fluorometric assay that can detect from 10 nM to 10 μM nitrite and is compatible with a 96-well microplate format.

Uses

2,3-Diaminonaphthalene is used in preparation of precursors for multi-layer 3D material comprising chiral organic sandwich compounds.

Reactions

2,3-diaminonaphthalene (DAN) is a fluorometric probe for nitrite. It reacts with nitrosonium, which is formed from nitrite at low pH, to form the fluorescent dye 1 H-naphthotriazole. This method can be used to detect 10 nM to 10 uM of nitrite (NO2-) and is compatible with 96-well format.
Reaction of 2,3-Diaminonaphthalene with NO2
Reaction of 2,3-Diaminonaphthalene with NO2.

Synthesis

2,3-DICHLORONAPHTHALENE

2050-75-1

 2,3-diaminonaphthalene

771-97-1

General procedure for the synthesis of 2,3-diaminonaphthalene from 2,3-dichloronaphthalene: Dissolve 2,3-dichloronaphthalene (2 g) in anhydrous ethanol. Ammonium chloride (1.5 g) was added and diluted. Subsequently, a catalytic amount of hydrochloric acid and an excess of concentrated aqueous ammonia solution were added to the reaction system and the reaction was refluxed on a water bath for 6 hours until the reaction solution showed a persistent dark green color. After completion of the reaction, the reaction solution was cooled and placed in a deep freezer overnight. Green crystals were obtained by filtration, dried and recrystallized with methanol. Dark green crystals were obtained; 75% yield; thin layer chromatography Rf values of 0.89 and 0.82; melting point 150 °C; IR spectra (νmax, KBr, cm-1): 758, 854, 1473 (aromatic C-N stretching vibration), 1500 (aromatic C=C stretching vibration), 1681 (N-H bending vibration), 3049 (N-H stretching vibration); 1H NMR (CDCl3, 500 MHz): δ 7.45-7.46 (dd, J=3.5-4 Hz, 2H, Ar-H), 7.12-7.14 (dd, J=3-3.5 Hz, 2H, Ar-H), 7.09 (s, 2H, Ar-H), 7.05 (s, 4H, Ar-NH2).

Purification Methods

Crystallise the diamine from water, or dissolve it in 0.1M HCl, by heating to 50o. After cooling, the solution is extracted with decalin to remove fluorescent impurities and centrifuged. [Beilstein 13 IV 346.]

References

[1] Oriental Journal of Chemistry, 2017, vol. 33, # 2, p. 821 - 828

2050-75-1
771-97-1
Synthesis of 2,3-diaminonaphthalene from 2,3-DICHLORONAPHTHALENE
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View Lastest Price from 2,3-diaminonaphthalene manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2,3-DIAMINONAPHTHALENE pictures 2026-03-20 2,3-DIAMINONAPHTHALENE
771-97-1
US $10.00 / KG 100KG 99% 100 mt Hebei Chuanghai Biotechnology Co., Ltd
2,3-diaminonaphthalene pictures 2025-12-01 2,3-diaminonaphthalene
771-97-1
US $0.00 / kg 1kg 99% 10000KGS Shaanxi Dideu New Materials Co. Ltd
2,3-diaminonaphthalene pictures 2025-12-01 2,3-diaminonaphthalene
771-97-1
US $0.00 / kg 1kg 99% 10000KGS Shaanxi Dideu New Materials Co. Ltd
2,3-Diaminonaphthalene(ForNoDetection) NAPHTHALENEDIAMINE TIMTEC-BB SBB000127 Naphthalene-2,3-diamine 2,3-Diaminonaphthalene,97% 2,3-Diaminonapthalene 2,3-DiaMinonaphthalene, 97% 1GR 2,3-DiaMinonaphthalene, 97% 5GR 2,3-DiaMinonaphthalene [for BiocheMical Research] DAN 2,3-Naphthalenediamine Diaminonaphthalene test solution(ChP) 2,3-NAPHTHYLENEDIAMINE 2,3-NAPHTHALENEDIAMINE 2,3-DIAMINONAPHTHALENE 2,3-Diaminonaphthalene *CAS 771-97-1* DAN JACS-771-97-1 2,3-Diaminonaphthalene > 2,3-Diaminonaphthalene[forBiochemicalResearch]> 2,3-DiaminonaphthaL 2,3-DIAMINONAPHTHALENE ISO 9001:2015 REACH Diaminonaphthalene test solution 2,3-DIAMINONAPHTHALENE Extra Pure DAN, Fluorescence determination of NO2- 2,3-Diaminonaphthalene, 10 mM in DMSO DAND1 Dapoxetine Impurity 129 771-97-1 771-91-1 Nitric Oxide and Oxygen Probes Nitric Oxide Probes Fluorescent Indicators and Probes Fluorescent Probes, Labels, Particles and Stains Biochemicals and Reagents BioChemical Naphthalene derivatives