3,4-Dihydro-2,2-dimethyl-2H-pyrrol-1-oxid

5,5-dimethyl-1-pyrroline N-oxide

HCID 1774CAS 3317-61-1

Grundinformationen

Standard-SMILES
CC1(C)CCC=[N+]1[O-]
InChIKey
VCUVETGKTILCLC-UHFFFAOYSA-N
Summenformel
C6H11NO
Durchschnittliche Molmasse
113,16 g/mol
Monoisotopische Masse
113,08406397

Überblick

5,5-dimethyl-1-pyrroline N-oxide is a member of the class of 1-pyrroline nitrones (1-pyrroline N-oxides) resulting from the formal N-oxidation of 5,5-dimethyl-1-pyrroline. Used as a spin trap for the study of radicals formed by enzymatic acetaldehyde oxidation. It has a role as a spin trapping reagent and a neuroprotective agent. It is functionally related to a 5,5-dimethyl-1-pyrroline.

Namen und Bezeichner

Bevorzugter Name
5,5-dimethyl-1-pyrroline N-oxide
IUPAC
2,2-dimethyl-1-oxido-3,4-dihydropyrrol-1-ium
Lokaler Name
3,4-Dihydro-2,2-dimethyl-2H-pyrrol-1-oxid
Englischer Name
5,5-Dimethyl-1-pyrroline N-oxide
Summenformel
C6H11NO
Molmasse
113.16

Namen und Synonyme

3317-61-15,5-Dimethyl-1-pyrroline N-oxideDMPO5,5-Dimethyl-1-pyrroline-N-oxide5,5-Dimethyl-1-pyrroline-1-oxide5,5-Dimethylpyrroline-N-oxide7170JZ1QF3CHEBI:1494895,5-DMPODMPO-5,5RefChem:101036222-011-1
Weitere Namen anzeigen
3,4-DIHYDRO-2,2-DIMETHYL-2H-PYRROLE 1-OXIDEDimethyl NspintrappingreagentDMPO, hydrophilic spin trap,5-Dimethyl-1-pyrroline N-oxide5.5-Dimethyl-1-pyroline n-oxide
2,2-Dimethyl-3,4-dihydro-2H-pyrrole 1-oxide2,2-dimethyl-1-oxido-3,4-dihydropyrrol-1-iumMFCD000052792H-Pyrrole, 3,4-dihydro-2,2-dimethyl-, 1-oxide5,5-Dimethyl-1-Pyrrolidine-N-oxideDMPO [MI]Lopac0_000350SCHEMBL130517

Datenbank-Bezeichner

CAS
3317-61-1
PubChem CID
1774
DTXSID
DTXSID30186826
ChEMBL
CHEMBL79824
ChEBI
CHEBI:149489
UNII
7170JZ1QF3
EC Number
222-011-1
Nikkaji
J205.397G

Eigenschaften

Berechnete Struktureigenschaften

XLogP
-0,3
Polarare Oberfläche (TPSA)
28,8 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
1
Frei drehbare Bindungen
0
Schwere Atome
8

Experimentelle und physikochemische Eigenschaften

Chemical ClassesOther Uses -> Biochemical Research
Physical DescriptionWhite solid; Highly hygroscopic; [Merck Index] Light yellow, hygroscopic solidified mass or fragments; mp = 25-29 deg C; [Sigma-Aldrich MSDS]

Physikochemische Eigenschaften

Schmelzpunkt
25 · 25-29 °C (lit.)
Siedepunkt
75 °C/0.4 · 75 °C/0.4 mmHg (lit.)
Dichte
1.015 g/mL · 1.015 g/mL at 25 °C (lit.)
Brechungsindex
20 · n20/D 1.496(lit.)
Flammpunkt
204 °F · 204 °F
storage temp.
-20 °C · -20°C

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 3 Einträge

This chemical does not meet GHS hazard criteria for 100% (2 of 2) of all reports.

Not Classified

Aggregated GHS information provided per 2 reports by companies from 1 notifications to the ECHA C&L Inventory.

Gefahrenhinweise

Hazards SummaryMay cause irritation; [Sigma-Aldrich MSDS]
Hazard Classes and CategoriesNot Classified

Sicherheitsdaten

F
8-10
wgk
3
hs_code
29339900
safety_code
24/25
hazard_class
IRRITANT
Speicherklasse
10 - Combustible liquids

Chemie und Industrie

Verwendung und Herstellung

UsesUsed in biology as a spin trap agent; [Merck Index]
Anwendungen · 2 Einträge

BeschreibungFree radicals are highly reactive, short-lived species. Spin traps react with radicals, forming stable adducts that can be further studied. DMPO is a commonly-used spin trap that reacts with O-, N-, S-, and C-centered radicals. This allows their characterization when used in association with electron spin resonance and immuno-spin trapping. DMPO is water-soluble, rapidly penetrates lipid bilayers, has low toxicity, and can be used in vitro and in vivo.

Verwenden5,5-Dimethyl-1-pyrroline N-oxide is a reagent generally used either as a free-radical spin-trapping agent, or electrophilic component during the synthesis of pyrrolidine derivatives. It may also be considered as 1,3-dipole in cycloaddition processes.

Darstellung · 1 Eintrag

synthetischeTo a three-necked round bottom flask equipped with a condenser, addi­tion funnel, thermometer, and mechanical stirrer and containing 300 ml. 95% ethanol precooled to 2°C is added, all at once, 14.5 g (0.1 mole) 4-methyl-4-nitropentanol, and 13.1 g (1.2 mole) zinc dust. With rapid agita­tion, the glacial acetic acid (24.0 g, 0.4 mole) is added dropwise over a 1-hr period while maintaining the reaction temperature below 15°C. The mix­ture is stirred vigorously for 2 hr and then stored in the refrigerator for 2 days, at approximately 1°C. Then the zinc acetate is filtered and rinsed with 100 ml of ethanol. The combined ethanol factions are rotoevapo-rated to give the crude nitrone. The crude nitrone is dissolved in a 200 ml portion of dichloromethane and the latter washed two times with saturated sodium bicarbonate solution. The organic layer is dried over sodium sul­fate and the solvent rotoevaporated, to give 10.7 (94% yield) of the crude nitrone. The product was purified by double distillation (b.p. 53°C, 0.1 Torr), to give 6.8 g (60%) of the pure nitrone as a white hygroscopic solid. The H1 NMR (400 MH CDC13, Me4Si) is 6.80 (t, 2H, methylene bound to quaternary C, J = 7.2Hg), 1.43 (s, 6H, methyl), C13NMr (100 MH2, CDC13, Me4 Si) 5=132.4 (Vinyl), 73.5 (quaternary), 34.1 (Allyl), 25.3 (methylene bound to quaternary C), 24.4 (methyls).

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