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Merck
CN

238619

3-Methyl-2-butanone

99%

Synonym(s):

Isopropyl methyl ketone, Methyl isopropyl ketone

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About This Item

Linear Formula:
(CH3)2CHCOCH3
CAS Number:
Molecular Weight:
86.13
EC Number:
209-264-3
UNSPSC Code:
12352103
PubChem Substance ID:
Beilstein/REAXYS Number:
1071238
MDL number:
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InChI key

SYBYTAAJFKOIEJ-UHFFFAOYSA-N

InChI

1S/C5H10O/c1-4(2)5(3)6/h4H,1-3H3

SMILES string

CC(C)C(C)=O

assay

99%

form

liquid

Quality Level

bp

94-95 °C (lit.)

mp

−92 °C (lit.)

density

0.805 g/mL at 25 °C (lit.)

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pictograms

Flame

signalword

Danger

hcodes

Hazard Classifications

Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

30.2 °F

flash_point_c

-1 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Huaqing Duan et al.
Organic & biomolecular chemistry, 13(24), 6782-6788 (2015-05-27)
A simple and efficient strategy for the synthesis of indane-1,3-dione derivatives through a palladium(0)-catalyzed reaction incorporating tert-butyl isocyanide has been developed. In addition, by applying this protocol as the key step, indenopyrazole derivatives can be easily synthesized in high yields
Yang Xia et al.
Journal of neuroinflammation, 12, 155-155 (2015-09-05)
Neuroendoscopy is an innovative technique for neurosurgery that can nonetheless result in traumatic brain injury. The accompanying neuroinflammation may lead to secondary tissue damage, which is the major cause of delayed neuronal death after surgery. The present study investigated the
Sami Sajjadifar et al.
Molecules (Basel, Switzerland), 15(4), 2491-2498 (2010-04-30)
Methyl indolenines (4a-c) and(5a-c) were prepared in high yield by a Fischer indole synthesis reaction of o,m-tolylhydrazine hydrochlorides (1a-b) with isopropyl methyl ketone (2) and 2-methylcyclohexanone (3) in acetic acid at room temperature. o,p- Nitrophenylhydrazines (1c-d) were reacted with 2-methylcyclohexanone
E M Gagan et al.
Archives of environmental contamination and toxicology, 52(3), 283-293 (2007-01-27)
Frequently the toxicity of an organic chemical mixture is close to dose-additive, even when the agents are thought to induce toxicity at different molecular sites of action. These findings appear to conflict with the hypothesis that a strictly dose-additive combined
Henry C Tseng et al.
Neurobiology of aging, 36(6), 2201-2212 (2015-03-31)
Primary open-angle glaucoma (POAG) is characterized by progressive neurodegeneration of retinal ganglion cells (RGCs). Why RGCs degenerate in low-pressure POAG remains poorly understood. To gain mechanistic insights, we developed a novel mouse model based on a mutation in human optineurin

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