534-26-9

Basic information

• Product Name: 2-METHYL-2-IMIDAZOLINE
• Synonyms: 1H-Imidazole,4,5-dihydro-2-methyl-;2-Imidazoline, 2-methyl-;2-methyl-2-imidazolin;2-Methyl-delta2-imidazoline;4,5-Dihydro-2-methyl-1H-imidazode;4,5-dihydro-2-methyl-1h-imidazol;4,5-Dihydro-2-methyl-1H-imidazole;Methyl glyoxaidine
• CAS NO: 534-26-9
• Molecular Formula: C₄H₈N₂
• Molecular Weight: 84.12
• EINECS: 208-596-6
• Product Categories: Heterocyclic Compounds
• Mol File: 534-26-9.mol
• Article Data: 23

Chemical Properties

• Melting Point: 87 °C (dec.)(lit.)
• Boiling Point: 144°C 140mm
• Flash Point: 197°C
• Appearance: White to yellow or colorless to yellow/Powder or Crystals or Needles
• Density: 0.8938 (rough estimate)
• Vapor Pressure: 0.493mmHg at 25°C
• Refractive Index: 1.5037 (estimate)
• PKA: 10.98±0.40(Predicted)
• Water Solubility: Soluble in water, alcohol, chloroform.
• Merck: 14,5635
• BRN: 104225
• CAS DataBase Reference: 2-METHYL-2-IMIDAZOLINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-METHYL-2-IMIDAZOLINE(534-26-9)
• EPA Substance Registry System: 2-METHYL-2-IMIDAZOLINE(534-26-9)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-37/39
• RIDADR: 1759
• WGK Germany: 3
• RTECS: NI4804995
• TSCA: Yes
• PackingGroup: III
• Hazardous Substances Data: 534-26-9(Hazardous Substances Data)

Usage

Uses

2-Methyl-2-imidazoline can be used as corrosion inhibitor.

General Description

Kinetics of the reaction of 2-methyl-2-imidazoline with sulfate and hydrogen phosphate radicals has been investigated by flash-photolysis. Rate constant for the reaction was reported to be 108-109M-1s-1.

InChI:InChI=1/C4H8N2/c1-4-5-2-3-6-4/h2-3H2,1H3,(H,5,6)/p+1

Upstream product

• 151-56-4 ethyleneimine 
• 75-05-8 acetonitrile 
• 62-55-5 thioacetamide 
• 107-15-3 ethylenediamine 
• 108-24-7 acetic anhydride 
• 4271-95-8 2-methyl-1,4,5,6-tetrahydropyrimidine 
• 1000-84-6 O-ethyl acetimidate 
• 927-80-0 1-ethoxyacetylene 
• 5504-00-7 N¹,N²-diphenylacetamidine hydrochloride 
• 39083-10-8 acetone oxime-o-benzenesulfonic ester 
• 127-09-3 sodium acetate 
• 18299-54-2 ethylenediamine hydrochloride 
• 871-78-3 N,N'-diacetylethylenediamine 
• 1001-53-2 monoacetylaminoethylamine 

Downstream Products

• 412277-89-5 N-acetyl-N-(2-benzamidoethyl)benzamide 
• 500014-64-2 1-[1-Methyl-2-(2-methyl-4,5-dihydroimidazol-1-ylmethyl)-1H-indol-5-yl]-3-(4-phenoxyphenyl)urea 
• 693-98-1 2-methylimidazole 
• 1001-53-2 monoacetylaminoethylamine 
• 21202-52-8 1-ethyl-2-methylimidazole 
• 693-98-1 2-methylimidazole 
• 4814-93-1 1-ethyl-2-methyl-4,5-dihydro-1H-imidazole 
• 615-15-6 2-Methyl-1H-benzimidazole 
• 930-61-0 2,4-dimethyl-2-imidazoline 
• 110698-57-2 N-{4-[2-(4,5-dihydro-2-methyl-1H-imidazol-1-yl)-1-oxoethyl]phenyl}methanesulfonamide 
• 127531-53-7 N-acetyl-N,N'-di-<2-(4-methoxycarbonyl)phenoxyethyl>ethylenediamine 
• 127531-52-6 1-<2-(4-methoxycarbonyl)phenoxyethyl>-2-methylimidazoline 
• 5053-43-0 2-methylpyrimidine 
• 54198-89-9 5-chloro-2-methylpyrimidine 

Relevant articles and documents

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INTRACELLULAR DELIVERY VEHICLE

PROBLEM TO BE SOLVED: To provide a vehicle which can easily deliver a desired component or compound into a cell without preventing cell proliferation. SOLUTION: A intracellular delivery vehicle has its surface covered with positive electric charge. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT

A Cell-Targeted Non-Cytotoxic Fluorescent Nanogel Thermometer Created with an Imidazolium-Containing Cationic Radical Initiator

A cationic fluorescent nanogel thermometer based on thermo-responsive N-isopropylacrylamide and environment-sensitive benzothiadiazole was developed with a new azo compound bearing imidazolium rings as the first cationic radical initiator. This cationic fluorescent nanogel thermometer showed an excellent ability to enter live mammalian cells in a short incubation period (10 min), a high sensitivity to temperature variations in live cells (temperature resolution of 0.02–0.84 °C in the range 20–40 °C), and remarkable non-cytotoxicity, which permitted ordinary cell proliferation and even differentiation of primary cultured cells.