144169
2,3-己二酮
technical grade, 90%
别名:
乙酰丁酰
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线性分子式:
CH3CH2CH2COCOCH3
化学文摘社编号:
分子量:
114.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
223-350-8
Beilstein/REAXYS Number:
1699896
MDL number:
Assay:
90%
Form:
liquid
产品名称
2,3-己二酮, technical grade, 90%
InChI key
MWVFCEVNXHTDNF-UHFFFAOYSA-N
InChI
1S/C6H10O2/c1-3-4-6(8)5(2)7/h3-4H2,1-2H3
SMILES string
CCCC(=O)C(C)=O
grade
technical grade
vapor density
3.9 (vs air)
vapor pressure
10 mmHg ( 20 °C)
assay
90%
form
liquid
refractive index
n20/D 1.412 (lit.)
bp
128 °C (lit.)
density
0.934 g/mL at 25 °C (lit.)
functional group
ketone
Quality Level
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Application
2,3-Hexanedione was used to evaluate the influence of xanthan concentration on the release of aroma compounds in xanthan-thickened food model systems.
General description
2,3-Hexanedione is a major component of the male-produced aggregation pheromone of Anelaphus inflaticollis Chemsak. It reacts with ethylenediamine to yield macrocyclic tetradentate 12-membered nitrogen donor (N4) ligand.
signalword
Warning
hcodes
Hazard Classifications
Flam. Liq. 3 - STOT RE 2 Inhalation
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
82.4 °F - closed cup
flash_point_c
28 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Sulekh Chandra et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 60(13), 3079-3085 (2004-10-13)
Complexes of Cr(III), Co(II), Ni(II) and Cu(II) containing a novel macrocyclic tetradentate nitrogen donor (N4) ligand prepared via reaction of 2,3-hexanedione and ethylenediamine has been prepared and characterized. The newly synthesized ligand (L) and its complexes have been characterized on
A M Ray et al.
Environmental entomology, 38(5), 1462-1466 (2009-10-15)
We report the identification and field bioassays of a major component of the male-produced aggregation pheromone of Anelaphus inflaticollis Chemsak, an uncommon desert cerambycine beetle. Male A. inflaticollis produced a sex-specific blend of components that included (R)-3-hydroxyhexan-2-one, (S)-2-hydroxyhexan-3-one, 2,3-hexanedione, and
Egle Bylaite et al.
Journal of agricultural and food chemistry, 53(9), 3577-3583 (2005-04-28)
The influence of xanthan concentration (0, 0.02, 0.1, 0.4, and 0.8% w/w) and bulk viscosity on the release of 20 aroma compounds of different chemical classes (5 aldehydes, 4 esters, 5 ketones, 3 alcohols, and 3 terpenes) was evaluated in
Thomas R Zilz et al.
Toxicology, 231(2-3), 210-214 (2007-01-19)
The potential cytotoxicity of two hexanedione food additives (2,3 and 3,4 isomers) was evaluated in comparison with the neurotoxic hexane metabolite 2,5-hexanedione in the human SK-N-SH neuroblastoma line using the MTT assay to indicate mitochondrial dehydrogenase activity and flow cytometry
Molecular mechanism of hexane neuropathy: significant differences in pharmacokinetics between 2.3-, 2.4-, and 2.5-hexanedione.
K Iwasaki et al.
Industrial health, 22(3), 177-187 (1984-01-01)
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