4480-47-1

Basic information

• Product Name: AKOS AKM00108
• Synonyms: 3,3-DIMETHYL-2-OXOBUTANAL;AKOS AKM00108;TERT-BUTYLGLYOXAL;NSC 409966
• CAS NO: 4480-47-1
• Molecular Formula: C₆H₁₀O₂
• Molecular Weight: 114.143
• Mol File: 4480-47-1.mol
• Article Data: 17

Chemical Properties

• Boiling Point: 128.2°C at 760 mmHg
• Flash Point: 34.4°C
• Appearance: /
• Density: 0.935g/cm³
• Vapor Pressure: 10.8mmHg at 25°C
• Refractive Index: 1.406
• CAS DataBase Reference: AKOS AKM00108(CAS DataBase Reference)
• NIST Chemistry Reference: AKOS AKM00108(4480-47-1)
• EPA Substance Registry System: AKOS AKM00108(4480-47-1)

Safety Data

• Hazardous Substances Data: 4480-47-1(Hazardous Substances Data)

Usage

General Description

AKOS AKM00108 is a chemical compound that is classified as an alkylphenol. It is commonly used as a surfactant and emulsifier in various industrial and consumer products, including detergents, paints, and lubricants. AKOS AKM00108 is known for its ability to reduce surface tension and enhance the mixing of different substances. Due to its efficient emulsifying properties, it is also utilized in the formulation of pesticides and herbicides. However, AKOS AKM00108 has been the subject of environmental and health concerns, as it has been found to persist in the environment and has potential endocrine-disrupting effects. Therefore, it is important to use this chemical with caution and consider safer alternatives when possible.

InChI:InChI=1/C6H10O2/c1-6(2,3)5(8)4-7/h4H,1-3H3

Upstream product

• 75-97-8 3,3-dimethyl-butan-2-one 
• 2987-16-8 3,3-dimethylbutyrylaldehyde 
• 7446-08-4 selenium(IV) oxide 
• 67-56-1 methanol 
• 22591-21-5 1,1-dichloro-3,3-dimethylbutan-2-one 
• 85692-37-1 1-(1-methyl-1H-imidazol-2-yl)ethan-1-one 
• 30263-65-1 1,1-dibromo-3,3-dimethylbutan-2-one 
• 5469-26-1 1-Bromopinacolon 

Downstream Products

• 6050-53-9 1-hydroxy-3,3-dimethyl-1-phenyl-butan-2-one 
• 6333-01-3 1-hydroxy-3,3-dimethyl-1-p-tolyl-butan-2-one 
• 855178-23-3 2-hydroxy-1-mesityl-3,3-dimethyl-butan-1-one 
• 800375-53-5 1-hydroxy-1-mesityl-3,3-dimethyl-butan-2-one 
• 94591-38-5 7-tert-Butyl-1,3-dimethyllumazin 
• 51440-69-8 5-(tert-butyl)pyrazine-2,3-dicarbonitrile 
• 4830-64-2 2-Hydroxy-2--1-tert.-butyl-aethanon-(1) 
• 38568-58-0 1-Methoxy-3,3-dimethyl-1-(4-nitro-benzenesulfonyl)-butan-2-one 
• 19909-71-8 1,2,3,4-Tetraoxo-1-tert.-butyl-4-phenyl-butan 
• 29574-90-1 1,3,4-Trioxo-2,2-dihydroxy-1-tert.-butyl-4-phenyl-butan (1,2,3,4-Tetraoxo-1-tert.-butyl-4-phenyl-butan-3-hydrat) 
• 66412-98-4 1-(p-chlorobenzamido)-3,3-dimethyl-1-hydroxy-butan-2-one 
• 815-17-8 trimethylpyruvic acid 
• 1354623-48-5 4-benzyl 3-tert-butyl (2S,4S)-2-tert-butyl-4-((R)-1-hydroxyallyl)oxazolidine-3,4-dicarboxylate 
• 1354623-46-3 4-benzyl 3-tert-butyl (2R,4R)-2-tert-butyl-4-((S)-1-(4-methoxybenzyloxy)allyl)oxazolidine-3,4-dicarboxylate 

Relevant articles and documents

Novel synthesis method of metribuzin intermediate

The invention discloses a novel synthesis method of a metribuzin intermediate, wherein the intermediate triazinone of metribuzin is produced by using pinacolone (methyl tert-butyl ketone) as an initial raw material through reaction steps of chlorination, hydrolysis, oxidation, condensation and the like. According to the invention, the reaction conditions are mild, and the total yield reaches 92.4%; hydrogen peroxide is used as an oxidizing agent for replacing sodium hypochlorite, and the oxidation reaction is carried out at a room temperature, so that the operation is convenient, and the byproduct is water so as to avoid the discharge of pollutants such as salt-containing wastewater and the like in the production process; and after the reaction is finished, the intermediate and the catalyst are subjected to chromatographic separation so as to recycle the water phase containing the catalyst.

Method for synthesizing tetra-2,3-(5-t-tutylpyrazine)metalloporphyrin

The invention relates to a method for synthesizing tetra-2,3-(5-t-tutylpyrazine)metalloporphyrin. The method comprises the following steps: using 3,3-dimethyl-2-butanone as a raw material, carrying out a selenizing reaction with selenium dioxide, and rectifying the product to obtain 3,3-dimethyl-2-oxobutryaldehyde; heating 3,3-dimethyl-2-oxobutryaldehyde obtained in the above step in the condition that 2,3-diamido-2-2-butene dinitrile, urea and metal chloride exist, and purifying the product to obtain the tetra-2,3-(5-t-tutylpyrazine)metalloporphyrin. According to the method, the tetra-2,3-(5-t-tutylpyrazine)metalloporphyrin can be obtained only through a two-step reaction of selenylation and synthesis and then through simple purification, the process is simple, and the product is controllable; the used raw materials are simple, and the cost is low; no poisonous or harmful waste product is produced in the middle process, so that the process of after-treatment is greatly reduced. The tetra-2,3-(5-t-tutylpyrazine)metalloporphyrin prepared in the invention is high in yield.