CAS 771-97-1|2,3-Diaminonaphthalene

Introduction:Basic information about CAS 771-97-1|2,3-Diaminonaphthalene, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Name2,3-Diaminonaphthalene
CAS Number771-97-1Molecular Weight158.200
Density1.2±0.1 g/cm3Boiling Point370.6±15.0 °C at 760 mmHg
Molecular FormulaC10H10N2Melting Point197-203 °C
MSDSChineseUSAFlash Point212.3±19.9 °C
Symbol
GHS07
Signal WordWarning

Names

Name2,3-diaminonaphthalene
SynonymMore Synonyms

2,3-Diaminonaphthalene BiologicalActivity

Description2,3 Diaminonaphthalene is a highly selective colorimetric and fluorometric reagent for selenium detection and also used for the fluorometric determination of nitrite.
Related CatalogSignaling Pathways >>Others >>OthersResearch Areas >>OthersDye Reagents
In VitroPoly(2,3-diaminonaphthalene) microspheres as a novel quencher for fluorescence-enhanced nucleic acid detection[1]. 2,3-Diaminonaphthalene (DAN) is possibly a carcinogenic reagent[2].
Kinase AssayVarious concentrations of each drug are incubated for 60 min at 37°C in OS-mL reaction volumes containing PBS (pH 7.4), 200 μM 2,3-Diaminonaphthalene (DAN) and 40 μM Sp/NO. Spermine/NO will spontaneously decompose at pH7.4 to produce 2 mol of NO and 1 mol of spermine with a half-life of 39 min at 37°C. Following the incubation period, 2.5 mL of 10 mM NaOH is added to each tube to stop the reaction. The NO-dependent N-nitrosation of 2,3-Diaminonaphthalene to yield its highly fluorescent N-nitrosated derivative, 2,3-naphthotriazole, is quantified by measuring the fluorescence of each sample using an excitation wavelength of 375 nm and an emission wavelength of 450nm. The concentration of Triazole is determined using standards of the pure 2,3-naphthotriazole[3].
References

[1]. Tian J, et al. Poly(2,3-diaminonaphthalene) microspheres as a novel quencher for fluorescence-enhanced nucleic acid detection. Analyst. 2011 Jun 7;136(11):2221-4.

[2]. Martínez-Tomé MJ, et al. Immobilization and characterization of 2,3-diaminonaphthalene/cyclodextrin complexes in a sol-gel matrix: a new fluorimetric sensor for nitrite. J Fluoresc. 2009 Jan;19(1):119-25.

[3]. Grisham MB, et al. Effects of aminosalicylates and immunosuppressive agents on nitric oxide-dependent N-nitrosation reactions. Biochem Pharmacol. 1994 May 18;47(10):1897-902.

Chemical & Physical Properties

Density1.2±0.1 g/cm3
Boiling Point370.6±15.0 °C at 760 mmHg
Melting Point197-203 °C
Molecular FormulaC10H10N2
Molecular Weight158.200
Flash Point212.3±19.9 °C
Exact Mass158.084396
PSA52.04000
LogP1.28
Vapour Pressure0.0±0.8 mmHg at 25°C
Index of Refraction1.757
InChIKeyXTBLDMQMUSHDEN-UHFFFAOYSA-N
SMILESNc1cc2ccccc2cc1N
Storage conditionRefrigerator
StabilityStable. Combustible. Incompatible with strong oxidizing agents.

Safety Information

Symbol
GHS07
Signal WordWarning
Hazard StatementsH302-H315-H319-H335
Precautionary StatementsP261-P305 + P351 + P338
Personal Protective Equipmentdust mask type N95 (US);Eyeshields;Gloves
Hazard CodesXn:Harmful;
Risk PhrasesR20/21/22;R36/37/38
Safety PhrasesS26
RIDADR2811
WGK Germany3
HS Code2921590090

Customs

HS Code2921590090
Summary2921590090. other aromatic polyamines and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

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Synonyms

2,3-Naphthalenediamine
naphthalene-2,3-diamine
2,3-Diaminonaphthalene
EINECS 212-241-0
MFCD00004116
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