10203-30-2

Basic information

• Product Name: 3-DODECANOL
• Synonyms: 3-DODECANOL;dodecan-3-ol
• CAS NO: 10203-30-2
• Molecular Formula: C₁₂H₂₆O
• Molecular Weight: 186.33
• Mol File: 10203-30-2.mol
• Article Data: 10

Chemical Properties

• Melting Point: 25°C
• Boiling Point: 250.85°C (estimate)
• Flash Point: 100.1 °C
• Appearance: /
• Density: 0.8223
• Vapor Pressure: 0.00476mmHg at 25°C
• Refractive Index: 1.4150 (estimate)
• PKA: 15.28±0.20(Predicted)
• CAS DataBase Reference: 3-DODECANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 3-DODECANOL(10203-30-2)
• EPA Substance Registry System: 3-DODECANOL(10203-30-2)

Safety Data

• Hazardous Substances Data: 10203-30-2(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Synthetic Communications, 19, p. 1833, 1989 DOI: 10.1080/00397918908052572

InChI:InChI=1/C12H26O/c1-3-5-6-7-8-9-10-11-12(13)4-2/h12-13H,3-11H2,1-2H3

Upstream product

• 112-40-3 dodecane 
• 110-42-9 Methyl decanoate 
• 925-90-6 ethylmagnesium bromide 
• 112-30-1 1-Decanol 
• 106-88-7 ethyloxirane 
• 111-83-1 1-bromo-octane 
• 1534-27-6 3-dodecanone 
• 112-31-2 caprinaldehyde 

Downstream Products

• 1534-27-6 3-dodecanone 

Relevant articles and documents

Grignard reagent/borohydride combinations alkylation/reduction of esters

The one step transformation of esters into secondary alcohols (70-80% yields) has been performed with a Grignard reagent in the presence of calcium or zinc borohydride. Under the same conditions, vinylic Grignard reagents gave γ,δ-unsaturated alcohols in good yields through three successive reactions: addition to the ester carbonyl, then conjugate addition and, finally reduction).

Hesperophylax occidentalis (Trichoptera: Limnephilidae): Electroantennogram structure-activity study of sex pheromone component 6-methylnonan-3-one

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A manganese-containing molecular sieve catalyst designed for the terminal oxidation of dodecane in air

MnIII ions that replace a few percent of the framework AlIII sites in a microporous aluminophosphate - number 18, with a pore aperture of 3.8 A - function as catalytically active centres for the selective oxidation of dodecane preferentially at C1 and C2.