Substance
ID:344897
Names and Identifiers
IUPAC name
1,3-dimethylimidazolidin-2-one
IUPAC Traditional name
1,3-dimethyl-2-imidazolidinone
Synonyms
N,N′-Dimethylethyleneurea1,3-二甲基-2-咪唑啉酮DMIN,N′-二甲基亚乙基脲DMEU1,3-Dimethyl-2-imidazolidinone
Registration numbers
EC Number
CAS Number
MDL Number
Beilstein Number
PubChem SID
Properties
Safety Information
GHS Pictograms
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
GHS Hazard statements
H302-H311-H315-H318
MSDS Link
European Hazard Symbols
Harmful (Xn)German water hazard class
3
RID/ADR
UN 2810 6.1/PG 3
Hazard Class
6.1
GHS Signal Word
Danger
Personal Protective Equipment
Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
RTECS
NJ0660000
UN Number
2810
Packing Group
3
Safety Statements
26-36
GHS Precautionary statements
P280-P305+P351+P338-P312
Risk Statements
21/22-38-41
Product Information
Empirical Formula (Hill Notation)
C5H10N2O
Grade
absolute
Quality
over molecular sieve (H2O ≤0.04%)
Purity
≥99.5% (GC)
Physical Property
Flash Point
102 °C
215.6 °F
Refractive Index
n20/D 1.472(lit.)
Boiling Point
224-226 °C(lit.)
Density
1.056 g/mL at 25 °C(lit.)
Molecule Details
Other Notes
Aprotic, dipolar solvent which often can be used as a substitute for the carcinogenic HMPA 1,2,3,4
Solvent used in various synthetic organic transformations. Studied in the formation of functionally stabilized hydrosilanediyl-transition metal complexes produced photochemically from arylsilanes.
Packaging
100, 500 mL in Sure/Seal™
Aprotic, dipolar solvent which often can be used as a substitute for the carcinogenic HMPA 1,2,3,4
Solvent used in various synthetic organic transformations. Studied in the formation of functionally stabilized hydrosilanediyl-transition metal complexes produced photochemically from arylsilanes.
Packaging
100, 500 mL in Sure/Seal™
Molecular Spectra
No Data Available
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References
No Data Available
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