90-30-2
90-30-2
Chemical Structure
N-Phenyl-1-naphthylamine
- CAS No.: 90-30-2
- Formula:C16H13N
- Molecular Weight:219.29
IUPAC Name: N-phenylnaphthalen-1-amine
InChIKey: XQVWYOYUZDUNRW-UHFFFAOYSA-N
SMILES: C12=CC=CC=C1C(NC3=CC=CC=C3)=CC=C2
Biological Activity: N-Phenyl-1-naphthylamine is a dye that fluoresces strongly when bound to the inner phospholipid bilayer of Gram-negative bacteria. N-Phenyl-1-naphthylamine can be used to measure outer membrane permeability. N-Phenylnaphthalen-1-amine is a fluorescence probe for odorant-binding proteins (OBP) with a dissociation constant of 1.67 μM. N-Phenylnaphthalen-1-amine exhibits an excitation wavelength of 337 nM and an emission wavelength of 407 nM[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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N-Phenyl-1-naphthylamine | 99.98% | N-Phenyl-1-naphthylamine is a dye that fluoresces strongly when bound to the inner phospholipid bilayer of Gram-negative bacteria. N-Phenyl-1-naphthylamine can be used to measure outer membrane permeability. N-Phenylnaphthalen-1-amine is a fluorescence probe for odorant-binding proteins (OBP) with a dissociation constant of 1.67 μM. N-Phenylnaphthalen-1-amine exhibits an excitation wavelength of 337 nM and an emission wavelength of 407 nM. | ||||||||||||||||||||
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Yellow AB | 99.45% | Yellow AB (Solvent yellow 5) is an azo dye that can be used as food dye. | ||||||||||||||||||||
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Sudan I (Standard) | ≥98% | Sudan I (Standard) is the analytical standard of Sudan I. This product is intended for research and analytical applications. Sudan I (Solvent Yellow 14) is a diazo-conjugate red dye and can be used as an additive to products such as oils, solvents or polishes. Sudan I inhibits growth of bacterial strains Clostridium perfringens and L. rhamnosus. | ||||||||||||||||||||
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ANS | 98.01% | ANS (8-Anilino-1-naphthalenesulfonic acid) is a competitive inhibitor targeting thyroxine binding globulin (TBG) (Ki=2.09×106 M-1). ANS is used in radioimmunoassay by displacing bound triiodothyronine (T3) to improve detection sensitivity. ANS can block the protein binding site of T3 and release free T3 for antibody recognition. As a fluorescent probe, ANS can specifically bind to the hydrophobic region of proteins (such as membrane proteins) and monitor the dynamics of protein conformation through changes in fluorescent signals. It is widely used in biochemical research and antibacterial material development. | ||||||||||||||||||||
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ANS ammonium | 99.94% | ANS ammonium is a potent antibacterial agent and a textile dye. ANS ammonium can be used as fluorescence probe. ANS ammonium blocks the binding of triiodothyronine to thyroxine binding globulin in radioimmunoassay of triiodothyronine. | ||||||||||||||||||||
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DPPD | 98.02% | DPPD (N,N′-Diphenyl-p-phenylenediamine) is an orally active antioxidant. DPPD also acts as a toxic substance and pregnancy disruptor. | ||||||||||||||||||||
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Triphenylamine | 99.68% | Triphenylamine (N,N-Diphenylbenzenamine) is a highly fluorescent compound. Triphenylamine can induce apoptosis. Triphenylamine can be used as a fluorescent dye and is also used in photodynamic therapy research. | ||||||||||||||||||||
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2-Nitrodiphenylamine | 99.87% | 2-Nitrodiphenylamine is a non-p-phenylenediamine aromatic amine antioxidant. 2-Nitrodiphenylamine can be used in antioxidant-related research. | ||||||||||||||||||||
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4-(Phenylazo)diphenylamine | 4-(Phenylazo)diphenylamine is an excellent colorimetric indicator for the accurate determination of the concentration for a variety of strong bases, Lewis acids, and hydride reducing agents. | |||||||||||||||||||||
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N-Phenyl-N'-(2-methylphenyl)-p-phenylenediamine | N-Phenyl-N'-(2-methylphenyl)-p-phenylenediamine is a metal-organic framework (MOF). | |||||||||||||||||||||
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References
- [1]. Ban L, et al., Biochemical characterization and bacterial expression of an odorant-binding protein from Locusta migratoria. Cell Mol Life Sci. 2003 Feb;60(2):390-400. [Content Brief]
- [2]. Vanderlinde EM, et al. Mutation of the sensor kinase chvG in Rhizobium leguminosarum negatively impacts cellular metabolism, outer membrane stability, and symbiosis. J Bacteriol. 2012 Feb;194(4):768-77. [Content Brief]
