66793-85-9

Basic information

• Product Name: 3-PROPYL-1-HEXANOL
• Synonyms: 3-PROPYL-1-HEXANOL;3-propyl-hexan-1-ol
• CAS NO: 66793-85-9
• Molecular Formula: C9H20O
• Molecular Weight: 144.25
• Mol File: 66793-85-9.mol
• Article Data: 3

Chemical Properties

• Melting Point: 6.15°C (estimate)
• Boiling Point: 192.9°C (estimate)
• Appearance: /
• Density: 0.8446 (estimate)
• Refractive Index: 1.4340
• CAS DataBase Reference: 3-PROPYL-1-HEXANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 3-PROPYL-1-HEXANOL(66793-85-9)
• EPA Substance Registry System: 3-PROPYL-1-HEXANOL(66793-85-9)

Safety Data

• Hazardous Substances Data: 66793-85-9(Hazardous Substances Data)

Upstream product

• 10297-65-1 3-propylhex-2-en-1-ol 
• 75-21-8 oxirane 
• 73999-15-2 3-propyl-hexanoic acid methyl ester 
• 10297-63-9 ethyl 3-propylhex-2-enoate 
• 156572-89-3 3-Propyl-2-hexenoic acid methyl ester 
• 23985-60-6 3-hydroxy-3-propyl-hexanoic acid 
• 123-19-3 4-heptanone 
• 21378-07-4 4-vinylheptan-4-ol 
• 682-28-0 3-propyl-hex-1-yn-3-ol 
• 10297-62-8 (3-Hyroxy-3-n-propyl)-capronsaeureethylester 

Relevant articles and documents

BRANCHED TAIL LIPID COMPOUNDS AND COMPOSITIONS FOR INTRACELLULAR DELIVERY OF THERAPEUTIC AGENTS

The application relates to lipids of Formula (A), Formula (B) and Formula (1-1), and to lipid nanoparticles (empty or loaded LNPs) including such a lipid as well as additional lipids such as phospholipids, structural lipids, and PEG lipids. Lipid nanoparticles further including therapeutic and/or prophylactics such as RNA are useful in the delivery of therapeutic and/or prophylactics to mammalian cells or organs to, for example, regulate polypeptide, protein, or gene expression.

Research in dipropylacetic series. XII. Aliphatic ramified acids and alcohols with anticonvulsant activity

Previous results obtained about 2 propyl pentanoic acid (dipropylacetic or DPA) have been extended to other dialkylalkanoic acids having less than 14 carbon atoms and to some of their precursors (alcohols) or derivatives (amides). The effect of lengthening the chain bonding between the carbon bearing the two alkyl chains and the functional carbon on about 50 molecules is discussed. The anticonvulsant activity's length and strength often increases when lengthening that chain.