9003-34-3

Basic information

• Product Name: VANAX PY
• Synonyms: 1,4-dinitroso-benzenhomopolymer;Benzene,1,4-dinitroso-,homopolymer;p-dinitroso-benzenpolymers;polyac;poly-p-dinitrosobenzene;VANAX PY;POLY-PARA-DINITROSOBENZENE;p-Dinitrosobenzene homopolymer
• CAS NO: 9003-34-3
• Molecular Formula: C6H4N2O2
• Molecular Weight: 136.10816
• Product Categories: Polymers
• Mol File: 9003-34-3.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 259.7°Cat760mmHg
• Flash Point: 103.5°C
• Appearance: /
• Density: 1.3g/cm³
• CAS DataBase Reference: VANAX PY(CAS DataBase Reference)
• NIST Chemistry Reference: VANAX PY(9003-34-3)
• EPA Substance Registry System: VANAX PY(9003-34-3)

Safety Data

• Safety Statements: Moderately toxic by ingestion. Mutation data reported. When heated to decomposition it emits toxic fumes of NO:
• Hazardous Substances Data: 9003-34-3(Hazardous Substances Data)

Usage

General Description

VANAX PY is a chemical compound that is a type of flame retardant. It is commonly used in various applications such as textiles, plastics, and electronics to improve fire resistance. VANAX PY works by releasing water vapor and carbon dioxide when it is exposed to high temperatures, which helps to reduce the spread and intensity of flames. Additionally, it is known for its low toxicity and environmental impact, making it a preferred choice for flame retardant applications. VANAX PY has been found to be effective in increasing the fire safety of a wide range of materials and products, making it a valuable chemical in the field of fire protection.

Upstream product

• 7664-93-9 sulfuric acid 
• 625-45-6 2-methoxyacetic acid 
• 106-51-4 p-benzoquinone 
• 106-50-3 1,4-phenylenediamine 
• 105-11-3 1,4-Benzochinondioxim 
• 105-11-3 p-benzoquinone dioxime 
• 52211-69-5 O,O'-bis(1,3,5-tri-tert-butyl-4-oxo-2,5-cyclohexadienyl)-p-benzoquinone dioxime 
• 57435-52-6 [1,4]Benzoquinone bis-[O-(1-tert-butoxy-3,5-di-tert-butyl-4-oxo-cyclohexa-2,5-dienyl)-oxime] 
• 24924-26-3 N,N'-dinitroso-1,4-phenylenedihydroxylamine 
• 108-95-2 phenol 

Downstream Products

• 101828-40-4 1,4-bis-[4-(4-amino-phenylazo)-phenylazo]-benzene 
• 21371-46-0 1,4-bis-(4-amino-phenylazo)-benzene 
• 96374-99-1 1,4-bis-[4-(phenyl-trans-azo)-phenyl-trans-azo]-benzene 
• 864849-80-9 1-(4-amino-phenylazo)-4-(4-amino-phenyl-NNO-azoxy)-benzene 
• 36369-22-9 1,4-bis-(phenyl-trans-azo)-benzene 
• 876500-17-3 1-(phenyl-NNO-azoxy)-4-(phenyl-ONN-azoxy)-benzene 
• 52211-69-5 O,O'-bis(1,3,5-tri-tert-butyl-4-oxo-2,5-cyclohexadienyl)-p-benzoquinone dioxime 
• 864849-81-0 1-(4-acetylamino-phenylazo)-4-(4-acetylamino-phenyl-NNO-azoxy)-benzene 
• 54915-73-0 1-phenylazo-4-(phenyl-NNO-azoxy)-benzene 
• 2294-47-5 1,4-diazidobenzene 

Relevant articles and documents

Preparation method for synthesizing p-dinitrosobenzene by wet material

The present application discloses a method for synthesizing p-nitrosobenzene by wet material, comprising: adding phenol to an aqueous solution of sodium nitrite and sodium hydroxide, formulated into a mixed solution of sodium phenol and sodium nitrite, at a predetermined temperature, the mixed solution is added dropwise to the sulfuric acid solution, stirring reaction, filtering, washing to obtain an intermediate p-nitrosophenol wet material; The p-benzoquinone dioxime wet material was dissolved in an aqueous solution of sodium hydroxide to obtain an alkaline p-benzoquinone dioxime solution, and the NaClO dilute solution was added dropwise to the alkaline p-benzoquinone dioxime solution, stirred the reaction, filtered and washed to obtain a p-nitrosobenzene product. The raw material cost of this method is low, the whole process involves only water as a reaction solvent, the operation process is simple, the process wet intermediates do not need to be dried, and the final p-dinitrosobenzene has excellent adhesive adhesion performance.

Selective N-oxidation of aromatic amines to nitroso derivatives using a molybdenum acetylide oxo-peroxo complex as catalyst

The molybdenum acetylide oxo-peroxo complex obtained in situ by the treatment of the corresponding molybdenum acetylide carbonyl complex, CpMo(CO)3(C{triple bond, long}CPh); Cp = η5-C5H5 with H2O2, has been used as an efficient catalyst for selective N-oxidation of primary amines to nitroso derivatives. Excellent amine conversion (up to 100%) and very high selectivity for nitroso compounds (99%) have been obtained using 30% hydrogen peroxide as an oxidant. The oxo peroxo Mo(VI) complex has also been found to be very active for the oxidation of various substituted primary aromatic amines with electron donating as well as electron withdrawing substituents on the aromatic ring.

KINETICS AND MECHANISM OF THE THERMAL DISSOCIATION OF O,O'-BIS(1,3,5-TRI-tert-BUTYL-4-OXO-2,5-CYCLOHEXADIENYL)-p-BENZOQUINONE DIOXIME IN SOLUTION

The kinetics and mechanism of the thermal dissociation of O,O'-bis(1,3,5-tri-tert-butyl-4-oxo-2,5-cyclohexadienyl)-p-benzoquinone dioxime (quinol ether) in solutions in nonpolar solvents were investigated.The dissociation of the quinol ether is a reversible two-stage process and involves the formation of an intermediate radical.In relation to the reaction conditions (initial concentration, temperature) the dissociation rate of the quinol ether obeys the kinetic equations ω = keff.c1/2 or ω = k1c.The change in the reaction order is due to the ratio of the rates of dissociation of the intermediate radical and of its reaction with the phenoxyl radical.