Substance

ID:177090

6-Methyl-2,4-heptanedione

Names and Identifiers
IUPAC name
6-methylheptane-2,4-dione
IUPAC Traditional name
6-methylheptane-2,4-dione
Synonyms
NSC 94IsovalerylacetoneNSC 464696-Methyl-2,4-heptanedione6-甲基-2,4-庚二酮NSC 42238NSC 42240
Registration numbers
Beilstein Number
MDL Number
PubChem SID
CAS Number
EC Number
Properties
Safety Information
GHS Signal Word
Warning
Storage Temperature
2-8°C
Hazard Class
3
GHS Pictograms
GHS07
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
GHS02
Flammable gases, category 1
Flammable aerosols, categories 1,2
Flammable liquids, categories 1,2,3
Self-reactive substances and mixtures, Types B,C,D,E,F
Pyrophoric liquids, category 1
Pyrophoric solids, category 1
Self-heating substances and mixtures
Substances and mixtures, which in contact with water, emit flammable gases, categories 1,2,3
Organic peroxides, Types B,C,D,E,F
Safety Statements
26-36
European Hazard Symbols
Irritant Irritant (Xi)
RID/ADR
UN 1993 3/PG 3
German water hazard class
3
Personal Protective Equipment
Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
UN Number
1993
GHS Hazard statements
H226-H315-H319-H335
Risk Statements
36/37/38
GHS Precautionary statements
P261-P305+P351+P338
Packing Group
3
Physical Property
Apperance
yellow
Flash Point
59 °C
138.2 °F
Density
0.92 g/mL at 25 °C(lit.)
Product Information
Purity
≥98%
Molecule Details
包装
25 g in glass bottle
Application
Reactant involved in:
• Cyclocondensation and deacetylation of dibromo(phenylsulfonyl)propene derivatives for synthesis of disubstituted furans1
• Synthesis of dual activity effectors of angiotensin II type 1 receptors and peroxisome proliferator-activated receptor-γ 2
• Addition reactions with 1-alkynes3
• Knoevenagel condensation4
• Oxidative free radical reactions with 2-amino-1,4-benzoquinones5
• Mild oxidative cleavage for synthesis of carboxylic acids6
Molecular Spectra
No Data Available
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References
No Data Available
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