10913
アセト酢酸メチル
Wacker Chemie AG, ≥99.0% (GC)
別名:
3-オキソブタン酸メチルエステル, アセト酢酸メチルエステル
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この商品について
化学式:
CH3COCH2COOCH3
CAS番号:
分子量:
116.12
EC Number:
203-299-8
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
506727
MDL number:
Assay:
≥99.0% (GC)
InChI key
WRQNANDWMGAFTP-UHFFFAOYSA-N
InChI
1S/C5H8O3/c1-4(6)3-5(7)8-2/h3H2,1-2H3
SMILES string
COC(=O)CC(C)=O
assay
≥99.0% (GC)
autoignition temp.
536 °F
manufacturer/tradename
Wacker Chemie AG
bp
169-170 °C/70 mmHg (lit.)
mp
−80 °C (lit.)
solubility
H2O: soluble 2 parts, alcohol: miscible, diethyl ether: miscible
density
1.076 g/mL at 25 °C (lit.)
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General description
Methyl acetoacetate undergoes asymmetric hydrogenation to form (R)-(-)-methyl-3-hydroxybutyrate in the presence of enantioselective Ni/SiO2 catalysts. It undergoes Pechmann reactions with phenols in various ionic liquids.
Application
Methyl acetoacetate was used in development of a simple and cost effective method for monitoring of trace formaldehyde in air. It was used to study the substrate specificity of NADPH-dependent diacetyl reductase in Escherichia coli.
Other Notes
バルク量の価格はお問い合わせください。
wgk
WGK 1
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
保管分類
10 - Combustible liquids
flash_point_f
158.0 °F - closed cup
flash_point_c
70 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
第4類:引火性液体 + 第三石油類 + 危険等級III + 非水溶性液体
fsl
名称等を表示すべき危険物及び有害物
ishl_indicated
名称等を通知すべき危険物及び有害物
ishl_notified
10913-VAR: + 10913-25KG: + 10913-220KG: + 10913-BULK: + 10913-1KG:
jan
The enantioselective hydrogenation of methyl acetoacetate over supported nickel catalysts: I. The modification procedure.
Keane MA and Webb G.
J. Catal., 136(1), 1-15 (1992)
P Silber et al.
Journal of bacteriology, 118(3), 919-927 (1974-06-01)
A reduced nicotinamide adenine dinucleotide phosphate (NADPH)-dependent reductase with the ability to reduce diacetyl has been isolated from Escherichia coli and has been purified 800-fold to near homogeneity. The product of the reduction of diacetyl was shown to be acetoin.
Pechmann reaction in non-chloroaluminate acidic ionic liquids under solvent-free conditions.
Gu Y, et al.
Advanced Synthesis & Catalysis, 347(4), 512-516 (2005)
Opas Bunkoed et al.
Analytica chimica acta, 659(1-2), 251-257 (2010-01-28)
We report the development of transparent sol-gels with entrapped sensitive and selective reagents for the detection of formaldehyde. The sampling method is based on the adsorption of formaldehyde from the air and reaction with beta-diketones (for example acetylacetone) in a
S Aramaki et al.
Journal of inherited metabolic disease, 14(1), 63-74 (1991-01-01)
The concentrations of 2-methylacetoacetate, 2-methyl-3-hydroxybutyrate and tiglylglycine were determined by gas chromatography-mass spectrometry in urine collected before and for 8 h after loading with 100 mg of isoleucine per kg of body weight. The sum of 2-methylacetoacetate and 2-butanone, a
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