1462-10-8

Basic information

• Product Name: 1,4-Pentanediol, 4-methyl-
• CAS NO: 1462-10-8
• Molecular Formula: C6H14O2
• Molecular Weight: 118.176
• Mol File: 1462-10-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,4-Pentanediol, 4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Pentanediol, 4-methyl-(1462-10-8)
• EPA Substance Registry System: 1,4-Pentanediol, 4-methyl-(1462-10-8)

Safety Data

• Hazardous Substances Data: 1462-10-8(Hazardous Substances Data)

Usage

Appearance

Colorless, odorless liquid

Physical State

Liquid

Solvent

Used in various chemical reactions and processes.

Precursor

In the production of resins, adhesives, and pharmaceuticals.

Plasticizer

Improves flexibility and durability of polymers.

Safety

Relatively safe for use in consumer products when handled and used properly.

Health Risks

Not known to pose significant health risks under proper handling and usage conditions.

Upstream product

• 107-18-6 allyl alcohol 
• 67-64-1 acetone 
• 64-18-6 formic acid 
• 930-39-2 2-cyclopropyl-2-propanol 
• 20924-80-5 2-allyl-2-methyl-oxirane 

Downstream Products

• 4830-05-1 3,3-Dimethyltetrahydro-2H-pyran-2-one 
• 1003-17-4 2,2-dimethyltetrahydrofuran 
• 763-89-3 4-methylpent-3-en-1-ol 
• 22508-64-1 4-methyl-4-penten-1-ol 
• 3123-97-5 dihydro-5,5-dimethyl-2(3H)-furanone 
• 1246448-17-8 5-(Bis(4-methoxyphenyl)(phenyl)methoxy)-2-methylpentan-2-ol 
• 1119-16-0 isocaproic aldehyde 
• 5362-52-7 4-methyl-pent-3-enal-(2,4-dinitro-phenylhydrazone) 
• 19327-72-1 4-methyl-pent-2t-enal-(2,4-dinitro-phenylhydrazone) 
• 5362-50-5 4-methyl-3-penten-1-al 
• 35144-28-6 4-(p-Anisyl)-4-methyl-1-chlorpentan 
• 2270-59-9 1-bromo-4-methylpent-3-ene 
• 78-70-6 3,7-dimethylocta-1,6-dien-3-ol 
• 88626-77-1 4-methyl-1-phenoxy-4-pentene 

Relevant articles and documents

Reaction Mechanism of Cathodic Crossed Coupling of Acetone with Unsaturated Compounds in Acidic Solution

It was confirmed that the cathodic crossed coupling of acetone with unsaturated compounds in aqueous sulfuric acid could proceed smoothly, when the compounds which had radical-acceptable double bonds and were adsorbed on a mercury cathode were used.From this fact, it was concluded that the coupling occurs via the addition of a radical intermediate formed by the one-electron reduction of acetone to the double bonds on the cathode surface.Possibility of the addition of an anionic intermediate derived from acetone was excluded by no occurrence of the coupling of acetone with a polar acetylenic triple bond compound adsorbed on the cathode.