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Home > Encyclopedia > 2-Ethyl-4-methylimidazole

2-Ethyl-4-methylimidazole

2-Ethyl-4-methylimidazole structure

2-Ethyl-4-methylimidazole 

structure
  • CAS No:

    931-36-2

  • Formula:

    C6H10N2

  • Chemical Name:

    2-Ethyl-4-methylimidazole

  • Synonyms:

    1H-Imidazole,2-ethyl-5-methyl-;Imidazole,2-ethyl-4-methyl-;1H-Imidazole,2-ethyl-4-methyl-;Imidazole,2-ethyl-4(or 5)-methyl-;2-Ethyl-5-methyl-1H-imidazole;2-Ethyl-4-methylimidazole;4-Methyl-2-ethylimidazole;2-Ethyl-4-methyl-1H-imidazole;EMI 24;Curezol 2E4MZ;2E4MZ;Epicure EMI 24;EMI 70;Imicure EMI 24;NSC 82315;Omicure 24EMI;B 2 (curing catalyst);B 2;JER Cure EMI 24;Dyhard MI-C;Curezol 2E4MZ2;Texnol EM 24;E 0232;65992-40-7;81833-71-8

  • Categories:

    Specialty Chemicals

Description

clear yellow viscous liquid after melting


Liquid

2-Ethyl-4-methylimidazole Basic Attributes

110.16

110.16

1711

213-234-5

5K8XI641G3

82315

DTXSID9044744

29339900

Characteristics

28.7

1.3

Liquid

1.0±0.1 g/cm3

47-54 °C(lit.)

120-125 °C @ Press: 2 Torr

280 °F

1.514

H2O: 210 g/L (20 ºC)

Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances. Store protected from moisture.

Safety Information

NONH for all modes of transport

2

22-41

26-39

NI6147500

Xn,Xi

Irritant/Harmful

Stable at room temperature in closed containers under normal storage and handling conditions.

P280-P305 + P351 + P338

H302-H318

|Danger|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P272, P280, P301+P312, P302+P352, P305+P351+P338, P310, P321, P330, P332+P313, P333+P313, P362, P363, and P501|Aggregated GHS information provided by 458 companies from 15 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P264, P280, P302+P352, P305+P351+P338, P310, P321, P332+P313, and P362|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

2-Ethyl-4-methylimidazole Use and Manufacturing

Methods of Manufacturing

The reaction of 1, 2-propanediamine and propionitrile produces 2-ethyl-4-methylimidazoline, which is then obtained by catalytic dehydrogenation.

Uses

Used for epoxy resin bonding, painting, pouring, encapsulating, dipping and composite materials, etc.


Intermediates

Pharmaceutical and medicine manufacturing|1H-Imidazole, 2-ethyl-5-methyl-: ACTIVE

Computed Properties

Molecular Weight:110.16
XLogP3:1.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:110.084398327
Monoisotopic Mass:110.084398327
Topological Polar Surface Area:28.7
Heavy Atom Count:8
Complexity:72.9
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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