41317-10-6

Basic information

• Product Name: 2-NITROSO-5-DIMETHYLAMINOPHENOL HYDROCHLORIDE
• Synonyms: 5-DIMETHYLAMINO-2-NITROSOPHENOL HYDROCHLORIDE;2-NITROSO-5-DIMETHYLAMINOPHENOL HYDROCHLORIDE;Nitrosodimethylaminophenolhydrochloride;2-Nitroso-5-dimethylaminophenol.HCl
• CAS NO: 41317-10-6
• Molecular Formula: C₈H₁₀N₂O₂*ClH
• Molecular Weight: 202.64
• Product Categories: Analytical Chemistry;Bipyridyls, etc. (Chelating Reagents);Chelating Reagents
• Mol File: 41317-10-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 337.6°C at 760 mmHg
• Flash Point: 158°C
• Appearance: /
• Vapor Pressure: 5.29E-05mmHg at 25°C
• Storage Temp.: Hygroscopic, -20°C Freezer, Under inert atmosphere
• Solubility: DMSO (Slightly, Heated, Sonicated), Methanol (Slightly), Water (Slightly)
• CAS DataBase Reference: 2-NITROSO-5-DIMETHYLAMINOPHENOL HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-NITROSO-5-DIMETHYLAMINOPHENOL HYDROCHLORIDE(41317-10-6)
• EPA Substance Registry System: 2-NITROSO-5-DIMETHYLAMINOPHENOL HYDROCHLORIDE(41317-10-6)

Safety Data

• Hazardous Substances Data: 41317-10-6(Hazardous Substances Data)

Usage

Description

2-Nitroso-5-dimethylaminophenol hydrochloride is a light-sensitive chemical compound that serves as a reducing agent in the development of photographic materials, producing metallic silver from silver halide grains. It also functions as a dye intermediate and a biological stain. Due to its potential health risks, it is crucial to handle this compound with care and implement appropriate safety measures during its use.

Uses

Used in Photographic Industry:
2-Nitroso-5-dimethylaminophenol hydrochloride is used as a light-sensitive agent for the development of photographic materials, where it acts as a reducing agent to produce metallic silver from silver halide grains, enabling the formation of images on photographic film or paper.
Used in Dye Industry:
2-Nitroso-5-dimethylaminophenol hydrochloride is used as a dye intermediate, contributing to the synthesis of various dyes that are utilized in different applications, such as textiles, plastics, and printing inks.
Used in Biotechnology and Scientific Research:
2-Nitroso-5-dimethylaminophenol hydrochloride is used as a biological stain, aiding in the visualization and identification of cellular structures and components in various biological and medical research applications. Its staining properties make it valuable for enhancing the contrast and detail in microscopic examinations.

InChI:InChI=1/C8H10N2O2.ClH/c1-10(2)6-3-4-7(9-12)8(11)5-6;/h3-5,11H,1-2H3;1H

Upstream product

• 99-07-0 3-Dimethylaminophenol 

Downstream Products

• 92510-34-4 7-dimethylamino-3-phenyl-2H-1,4-benzoxazin-2-one 
• 15103-39-6 2-amino-5-(dimethylamino)phenol 

Relevant articles and documents

N-(di)icosyl-substituted benzo[a]phenoxazinium chlorides: Synthesis and evaluation as near-infrared membrane probes

Five benzo[a]phenoxazinium chlorides containing alkyl chains with twenty carbon atoms at the 5- or 9-positions of the tetracyclic ring were efficiently synthesised and characterised by UV/Vis and NIR spectroscopy. The absorption and emission maxima in ethanol occur in the range 627-641 nm and 645-676 nm, respectively, with quantum yields varying from 0.14 to 0.38. Preliminary photophysical studies with these fluorochromophores in zwitterionic [2,3-bis(palmitoyloxy)propyl-2-(trimethylammonio)ethyl phosphate, DPPC] and cationic (N,N-dimethyl-N-octadecyloctadecan-1-aminium bromide, DODAB) vesicles were carried out. The results showed that the new benzo[a]phenoxazinium derivatives are able to detect the gel to liquid-crystalline lipid phase transition through variations in either the extent of H-aggregation or in the acid-base equilibrium. Novel benzo[a]phenoxazinium chlorides possessing icosyl groups as substituents at the 5- or 9-positions of the tetracyclic ring were photophysically studied in both zwitterionic and cationic vesicles. The results revealed that these fluorochromophores are able to detect the gel to liquid-crystalline lipid phase transition through variations either in the extent of H-aggregation or in an acid-base equilibrium. Copyright

LONG WAVELENGTH THIOL-REACTIVE FLUOROPHORES

Reactive fluorescent dyes compositions and methods of using same are disclosed. Squaraine nucleus, Nile red nucleus, benzodioxazole nucleus, coumarin nucleus or aza coumarin nucleus dyes are disclosed dyes are disclosed having thiol-reactive groups. Squaraine nucleus, Nile Red nucleus, benzodioxazole nucleus, coumarin nucleus or aza coumarin nucleus dyes are disclosed that exhibit a fluorescence emission of at least about 575 nm. Biosensors are disclosed having a binding protein and a squaraine nucleus, Nile Red nucleus, benzodiaxazole nucleus, coumarin nucleus or aza coumarin nucleus.