ChemicalBook--->CAS DataBase List--->1739-84-0

1739-84-0

1739-84-0 Structure

1739-84-0 Structure
IdentificationMore
[Name]

1,2-Dimethylimidazole
[CAS]

1739-84-0
[Synonyms]

1,2-dimethyl-1h-imidazole
1,2-DIMETHYLIMIDAZOLE
AKOS BBS-00004287
LUPRAGEN(R) DMI
1,2-dimethyl-1h-imidazol
1H-Imidazole,1,2-dimethyl-
Imidazole, 1,2-dimethyl-
1,2-Dimethylimdazole
N,2-DIMETHYLIMIDAZOLE
dimethylglyoxaline
1,2-Dimethylimidazol
39-41℃
1,2-Dimethylimidazole ,98%
[EINECS(EC#)]

217-101-2
[Molecular Formula]

C5H8N2
[MDL Number]

MFCD00005294
[Molecular Weight]

96.13
[MOL File]

1739-84-0.mol
Chemical PropertiesBack Directory
[Appearance]

colorless to yellow low melting mass
[Melting point ]

37-39 °C (lit.)
[Boiling point ]

204 °C (lit.)
[density ]

1.084 g/mL at 25 °C(lit.)
[vapor pressure ]

1 mm Hg ( 20 °C)
[refractive index ]

1.5000 (estimate)
[Fp ]

198 °F
[storage temp. ]

Store below +30°C.
[form ]

Low Melting Mass
[pka]

7.76±0.25(Predicted)
[color ]

Colorless to yellow
[Specific Gravity]

1.084
[Odor]

Amine-like odor
[PH]

12.6 (500g/l, H2O, 20℃)
[Water Solubility ]

Soluble in water.
[Detection Methods]

GC
[BRN ]

108457
[Henry's Law Constant]

4.3×101 mol/(m3Pa) at 25℃, Du et al. (2017)
[InChI]

1S/C5H8N2/c1-5-6-3-4-7(5)2/h3-4H,1-2H3
[InChIKey]

GIWQSPITLQVMSG-UHFFFAOYSA-N
[SMILES]

Cc1nccn1C
[LogP]

0.11 at 25℃
[CAS DataBase Reference]

1739-84-0(CAS DataBase Reference)
[NIST Chemistry Reference]

1H-Imidazole, 1,2-dimethyl-(1739-84-0)
[EPA Substance Registry System]

1739-84-0(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302-H315-H318
[Precautionary statements ]

P280-P305+P351+P338
[Hazard Codes ]

Xn,Xi
[Risk Statements ]

R22:Harmful if swallowed.
R38:Irritating to the skin.
R41:Risk of serious damage to eyes.
[Safety Statements ]

S24:Avoid contact with skin .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S2:Keep out of the reach of children .
[RIDADR ]

UN 3263 8/PG 2
[WGK Germany ]

2
[RTECS ]

NI4838854
[Autoignition Temperature]

896 °F
[TSCA ]

Yes
[REACH Registrations]

Active
[HazardClass ]

8
[PackingGroup ]

III
[HS Code ]

29332990
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Dam. 1
Skin Irrit. 2
[Toxicity]

LD50 orally in Rabbit: 1300 mg/kg
Raw materials And Preparation ProductsBack Directory
[Raw materials]

2-Methylimidazole-->1,2-Ethenediylbis(oxy) (9CI)-->Acetaldehyde-->Dimethyl carbonate-->Methylamine-->Ammonium hydroxide
[Preparation Products]

1,2-Dimethyl-1H-imidazole-5-carbaldehyde-->2-Methyl-2-imidazoline-->5-Bromo-1,2-dimethyl-1H-imidazole-->1-ethyl-2,3-diMethyliMidazoliuM iodide
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

1,2-Dimethylimidazole(1739-84-0).msds
Hazard InformationBack Directory
[Chemical Properties]

colorless to yellow low melting mass
[Uses]

1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
[Definition]

ChEBI: 1,2-dimethylimidazole is a member of imidazoles.
[General Description]

1,2-Dimethylimidazole reacts with copper(II) tetraacetate to yield cis-bis(acetato)bis(1,2-dimethylimidazole) copper(II) complex. It undergoes Menschutkin reaction with benzyl bromide to yield 3-benzyl-1,2-dimethylimidazolium bromide and kinetics of reaction was studied in various ionic liquids and molecular organic solvents.
[Flammability and Explosibility]

Notclassified
[Synthesis]

1,2-Ethenediylbis(oxy) (9CI)

131543-46-9

Acetaldehyde

75-07-0

Methylamine

74-89-5

1-Methylimidazole

616-47-7

1,2-Dimethylimidazole

1739-84-0

2-Methylimidazole

693-98-1

A high-pressure microreactor equipped with three micro-mixers was used for the synthesis. It was operated as follows: an aqueous methylamine solution (0.33 mol/L) was fed from tank 1 via pump 1 at a flow rate of 0.68 mL/min; an aqueous acetaldehyde solution (0.33 mol/L) was fed from tank 3 via pump 3A at a flow rate of 63 mL/min while nearby water (0.33 mol/L) flowed at a flow rate of 1.13 mL/min; an aqueous glyoxal solution ( 0.33 mol/L) was fed from tank 4 via pump 4 at a flow rate of 0.56 mL/min. The reaction pressure was set to 30 MPa and the final flow rate was 8.0 mL/min. The temperature of the first micro-mixer and the 2.4 m reaction tube was controlled at 25 °C by the thermostat chamber 1 , under which the mixing and reaction of methylamine with acetaldehyde was carried out. Subsequently, in the second micro-mixer, the reaction mixture was mixed with ammonia and kept at 25 °C in the constant temperature chamber 2, and the reaction was fully mixed and reacted in the 0.1 m reaction tube. Next, glyoxal was added to the reaction system and fully reacted in a 0 m reaction tube. Subsequently, the temperature of the reaction zone was raised to 70 °C and the reaction was continued in a 25 μm reaction tube. Finally, the reaction mixture was cooled to 5 °C by a heat exchanger, depressurized to atmospheric pressure by a pressure reducing valve, and the aqueous solution obtained under cooling in ice water (0 °C to 4 °C) was collected. The residence time of the reaction part was 37 seconds throughout the reaction. For analysis, the product was diluted 10-fold with ice water, if necessary, and analyzed immediately using a gas chromatograph. The reaction tube was made of stainless steel (SUS316) with an inner diameter of 0.5 mm. the yield of the product 1,2-dimethylimidazole was 85.1%. The quantitative analysis was performed on an Agilent gas chromatograph (GC 6890, hydrogen flame ionization detector) with an HP-INNOWAX column (inner diameter 0.32 mm, film thickness 0.25 μm, length 30 m) manufactured by J & W Co. The yield of each product (1,2-dimethylimidazole, 1-methylimidazole, 2-methylimidazole, and imidazole) was determined by preparing standard curves for each product. The yield of each product was calculated based on the concentration obtained by conversion of the standard curve as follows: 1,2-dimethylimidazole 85.1%, 1-methylimidazole 6.27%, 2-methylimidazole 6.59%, and imidazole 2.06%.

[Purification Methods]

Crystallise the imidazole from *benzene, dry and store it at 0-4o. The picrate crystallises from H2O or EtOH with m 181o. [Balaban & Pymann J Chem Soc 125 1570 1924, Gorun et al. J Am Chem Soc 109 4244 1987, Beilstein 23 H 66, 23 II 56, 23 III/IV 594.]
[References]

[1] Patent: JP2016/222615, 2016, A. Location in patent: Paragraph 0051-0052
Spectrum DetailBack Directory
[Spectrum Detail]

1,2-Dimethylimidazole(1739-84-0)MS
1,2-Dimethylimidazole(1739-84-0)1HNMR
1,2-Dimethylimidazole(1739-84-0)13CNMR
1,2-Dimethylimidazole(1739-84-0)IR1
1,2-Dimethylimidazole(1739-84-0)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

1,2-Dimethylimidazole, 98%(1739-84-0)
[Alfa Aesar]

1,2-Dimethylimidazole, 98%(1739-84-0)
[Sigma Aldrich]

1739-84-0(sigmaaldrich)
[TCI AMERICA]

1,2-Dimethylimidazole,>98.0%(GC)(1739-84-0)
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