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About This Item
Linear Formula:
CH3(CH2)7COCH3
CAS Number:
Molecular Weight:
156.27
Beilstein:
1747463
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
vapor density
>1 (vs air)
Quality Level
Assay
98%
form
liquid
refractive index
n20/D 1.425 (lit.)
bp
211 °C (lit.)
mp
3.5 °C (lit.)
density
0.825 g/mL at 25 °C (lit.)
SMILES string
CCCCCCCCC(C)=O
InChI
1S/C10H20O/c1-3-4-5-6-7-8-9-10(2)11/h3-9H2,1-2H3
InChI key
ZAJNGDIORYACQU-UHFFFAOYSA-N
Gene Information
human ... CES1(1066)
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General description
Microtox EC50 value of 2-decanone has been evaluated.
Application
2-Decanone was used in the synthesis of:
- brushed block copolymers via conjugation through an acid-labile hydrazone linker to poly(ethylene glycol)-poly(aspartate hydrazide) block copolymers
- methyl ketones
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point(F)
186.8 °F - closed cup
Flash Point(C)
86 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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A General Synthetic Method for the Preparation of Methyl Ketones from Terminal Olefins: 2-Decanone.
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Organic Syntheses, 9-9 (1984)
Hyun Jin Lee et al.
Pharmaceutical research, 30(8), 2077-2086 (2013-05-03)
To investigate the effects of small aliphatic pendent groups conjugated through an acid-sensitive linker to the core of brushed block copolymer micelles on particle properties. The brushed block copolymers were synthesized by conjugating five types of 2-alkanone (2-butanone, 2-hexanone, 2-octanone
H F Chen et al.
Ecotoxicology and environmental safety, 30(2), 120-123 (1995-03-01)
The Microtox EC50 values for the following ketones are reported in the following homologous series: straight chain methyl ketones (acetone, 2-butanone, 2-pentanone, 2-hepatonone, 2-octanone, 2-decanone, and 2-tridecanone); methyl ketones substituted at one alpha carbon (3-methyl-2-butanone; 3,3-dimethyl-2-butanone); methyl substituted at two
Erich M Staudacher et al.
Journal of neuroscience methods, 180(2), 208-223 (2009-05-26)
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Peter S Toth et al.
The Analyst, 140(6), 1947-1954 (2015-02-11)
Two-phase voltammetry has been carried out using a reverse cell configuration, i.e. with the lower density organic solvent on the top of the aqueous solution in the cell, where the organic solvents contain either nitrile or ketone functional groups. The
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