| Identification | Back Directory | [Name]
1-Methyl-5-nitro-1H-imidazole-2-methanol | [CAS]
936-05-0 | [Synonyms]
HMMNI
HMMNI Solution, 100ppm
dimetridazole-2-hydroxy
Dimetridazole-2-hydroxy D3
HMMNI (nitroimidazole metabolite)
1-Methyl-5-nitro-2-iMidazoleMethanol
1-methyl-5-nitroimidazole-2-methanol
HMMNI solution,1000ppm solution,100ppm
(3-methyl-2-nitroimidazol-4-yl)methanol
(3-methyl-2-nitro-imidazol-4-yl)methanol
1-methyl-5-nitro-1H-imidazole-2-methanol
1-Methyl-5-Nitro-2-Hydroxymethylimidazole
2-HYDROXYMETHYL-1-METHYL-5-NITRO-IMIDAZOLE
1H-Imidazole-2-methanol, 1-methyl-5-nitro-
(1-Methyl-5-nitro-1H-imidazo-2-yl)-methanol
(1-Methyl-5-nitro-1H-imidazole-2-yl)methanol
(1-METHYL-5-NITRO-1H-IMIDAZOL-2-YL)-METHANOL
2-HYDROXYMETHYL-1-METHYL-5-NITRO-1H-IMIDAZOLE
HMMNI,2-Hydroxymethyl-1-methyl-5-nitro-1H-imidazole | [EINECS(EC#)]
213-312-9 | [Molecular Formula]
C5H7N3O3 | [MDL Number]
MFCD00159675 | [MOL File]
936-05-0.mol | [Molecular Weight]
157.13 |
| Chemical Properties | Back Directory | [Melting point ]
110-112°C | [Boiling point ]
281.76°C (rough estimate) | [density ]
1.4890 (rough estimate) | [refractive index ]
1.6190 (estimate) | [storage temp. ]
-20?C Freezer | [solubility ]
DMF: 30 mg/ml; DMSO: 30 mg/ml; Ethanol: 3 mg/ml; PBS (pH 7.2): 1 mg/ml | [form ]
neat | [pka]
13.31±0.10(Predicted) | [color ]
Light yellow to Yellow to Orange | [InChI]
InChI=1S/C5H7N3O3/c1-7-4(3-9)6-2-5(7)8(10)11/h2,9H,3H2,1H3 | [InChIKey]
JSAQDPJIVQMBAY-UHFFFAOYSA-N | [SMILES]
C1(CO)N(C)C([N+]([O-])=O)=CN=1 |
| Hazard Information | Back Directory | [Chemical Properties]
Pale Yellow Solid | [Uses]
A metabolite of Dimetridazole (D479660). | [Description]
Dimetridazole is a nitroimidazole-based compound with antibacterial and anticoccidial activity.1 It was once widely used in the treatment of parasitic infections in poultry, cattle, swine and farmed fish until suspected to be carcinogenic and mutagenic to humans.2 Hydroxy dimetridazole is a metabolite of dimetridazole that may be useful for identifying this nitroimidazole in various agricultural samples through liquid chromatography–tandem mass spectrometry and other methods.2,3,4 | [Synthesis]
In a sealed glass tube, formaldehyde (1 g, 33.54 mmol) and 1-methyl-5-nitro-1H-imidazole (4a) (1 g, 7.8 mmol) were dissolved in DMSO (5 mL). The reaction tube was heated in an oil bath at 140°C for 48 hours. Upon completion of the reaction, the reaction solution was poured into water (5 mL) and extracted with ethyl acetate (3 x 5 mL). The organic phases were combined and dried with anhydrous magnesium sulfate, followed by concentration under reduced pressure to remove the solvent to give the crude product. The crude product was purified by recrystallization via THF/heptane (1:1) mixed solvent to afford the target product 1-methyl-5-nitro-2-hydroxymethylimidazole (5a) (0.76 g, 62% yield) in white powder form. The melting point of the product was 117°C. | [References]
[1] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1987, p. 2819 - 2828
[2] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 3, p. 1015 - 1018
[3] Journal of Medicinal Chemistry, 2003, vol. 46, # 3, p. 427 - 440
[4] Tetrahedron, 2000, vol. 56, # 4, p. 645 - 657
[5] Patent: WO2014/205414, 2014, A1. Location in patent: Paragraph 0298 |
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