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Thermo Scientific Chemicals
2,3-Diaminonaphthalene, 97%
CAS: 771-97-1 | C10H10N2 | 158.204 g/mol
化学物質識別子
CAS771-97-1
IUPAC Namenaphthalene-2,3-diamine
Molecular FormulaC10H10N2
InChI KeyXTBLDMQMUSHDEN-UHFFFAOYSA-N
SMILESNC1=C(N)C=C2C=CC=CC2=C1
さらに表示
仕様
スペックシート
スペックシートFormCrystals or powder or crystalline powder
Identification (FTIR)Conforms
Appearance (Color)Green to brown
Assay from Suppliers CofA≥96.0% (HPLC)
Melting Point (clear melt)190.0-199.0°C
さらに表示
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.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
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.
Solubility
Slightly soluble in water. Soluble in pyridine, dimethylsulfoxide, dimethyformamide, dil.hydrochloric acid, ethanol, ether and hot methanol.
Notes
Incompatible with oxidizing agents and acids.
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.
Solubility
Slightly soluble in water. Soluble in pyridine, dimethylsulfoxide, dimethyformamide, dil.hydrochloric acid, ethanol, ether and hot methanol.
Notes
Incompatible with oxidizing agents and acids.
RUO – Research Use Only
General References:
- Tian, J.; Zhang, Y.; Luo, Y.; Li, H.; Zhai, J.; Sun, X. Poly(2,3-diaminonaphthalene) microspheres as a novel quencher for fluorescence-enhanced nucleic acid detection. Analyst 2011, 136 (11), 2221-2224.
- Hasaninejad, A.; Firoozi, S.; Mandegani, F. An efficient synthesis of novel spiro[benzo[c]pyrano[3,2-a]phenazines] via domino multi-component reactions using l-proline as a bifunctional organocatalyst. Tetrahedron Lett. 2013, 54 (22), 2791-2794.
- Wang, Z.; Teoh, S. H.; Hong, M.; Luo, F.; Teo, E. Y.; Chan, J. K. Y.; Thian, E. S. Dual-Microstructured Porous, Anisotropic Film for Biomimicking of Endothelial Basement Membrane. ACS Appl. Mater. Interfaces 2015,7 (24), 13445-13456.
- Hirano, K.; Kobayashi, T. Quantitatively chemo-fluorometry diagnostic to nitrite ion in ultrasound aqueous medium containing 2,3-diaminonaphthalene. Ultrason. Sonochem. 2015, 26, 345-350.