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534-26-9

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534-26-9 Usage

Description

2-METHYL-2-IMIDAZOLINE is an organic compound with the molecular formula C4H8N2. It is characterized by its imidazoline ring structure, which is a five-membered ring containing two nitrogen atoms and three carbon atoms, with one additional methyl group attached to the second carbon atom. 2-METHYL-2-IMIDAZOLINE has been studied for its reaction kinetics with sulfate and hydrogen phosphate radicals, showing a rate constant in the range of 108-109M-1s-1.

Uses

Used in Corrosion Inhibition:
2-METHYL-2-IMIDAZOLINE is used as a corrosion inhibitor for various applications, particularly in the protection of metals and alloys from the detrimental effects of corrosion. Its ability to form a protective layer on the metal surface and its interaction with the corrosive agents make it an effective additive in the industry.
Used in Chemical Industry:
In the chemical industry, 2-METHYL-2-IMIDAZOLINE is used as a building block for the synthesis of various compounds and materials. Its unique structure and reactivity make it a valuable intermediate in the production of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Research and Development:
Due to its interesting chemical properties and reactivity, 2-METHYL-2-IMIDAZOLINE is also utilized in research and development for the exploration of new chemical reactions, mechanisms, and applications. Its study contributes to the advancement of knowledge in organic chemistry and related fields.

Check Digit Verification of cas no

The CAS Registry Mumber 534-26-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 534-26:
(5*5)+(4*3)+(3*4)+(2*2)+(1*6)=59
59 % 10 = 9
So 534-26-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H8N2/c1-4-5-2-3-6-4/h2-3H2,1H3,(H,5,6)/p+1

534-26-9 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (A15113)  2-Methyl-2-imidazoline, 97+%   

  • 534-26-9

  • 25g

  • 985.0CNY

  • Detail
  • Alfa Aesar

  • (A15113)  2-Methyl-2-imidazoline, 97+%   

  • 534-26-9

  • 100g

  • 3334.0CNY

  • Detail
  • Alfa Aesar

  • (A15113)  2-Methyl-2-imidazoline, 97+%   

  • 534-26-9

  • 500g

  • 13352.0CNY

  • Detail
  • Aldrich

  • (375403)  2-Methyl-2-imidazoline  95%

  • 534-26-9

  • 375403-5G

  • 374.40CNY

  • Detail

534-26-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-2-imidazoline

1.2 Other means of identification

Product number -
Other names 1H-Imidazole, 4,5-dihydro-2-methyl-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:534-26-9 SDS

534-26-9Relevant articles and documents

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Magosch

, p. 37 (1972)

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INTRACELLULAR DELIVERY VEHICLE

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Paragraph 0166; 0170-0171, (2020/08/13)

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

Uchiyama, Seiichi,Tsuji, Toshikazu,Kawamoto, Kyoko,Okano, Kentaro,Fukatsu, Eiko,Noro, Takahiro,Ikado, Kumiko,Yamada, Sayuri,Shibata, Yuka,Hayashi, Teruyuki,Inada, Noriko,Kato, Masaru,Koizumi, Hideki,Tokuyama, Hidetoshi

supporting information, p. 5413 - 5417 (2018/04/09)

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.

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