3,3-DIMETHYL-1-(2-CARBOXYPHENYL)TRIAZENE

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3,3-DIMETHYL-1-(2-CARBOXYPHENYL)TRIAZENE

  • Name 3,3-DIMETHYL-1-(2-CARBOXYPHENYL)TRIAZENE
  • CAS 20119-28-2
  • Purity 99%
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Product Details

99% Purity Commercial production 3,3-DIMETHYL-1-(2-CARBOXYPHENYL)TRIAZENE 20119-28-2 with Cheapest Price

  • Molecular Formula: C9H11N3O2
  • Molecular Weight: 193.205
  • Vapor Pressure: 7.64E-05mmHg at 25°C 
  • Melting Point: 124-126oC 
  • Boiling Point: 328.5°Cat760mmHg 
  • Flash Point: 152.4°C 
  • PSA: 65.26000 
  • Density: 1.19g/cm3 
  • LogP: 1.94510 

3,3-DIMETHYL-1-(2-CARBOXYPHENYL)TRIAZENE(Cas 20119-28-2) Usage

General Description

3,3-DIMETHYL-1-(2-CARBOXYPHENYL)TRIAZENE, also known as Methyl Red, is a synthetic organic compound primarily used as a pH indicator. It is a red powder that changes color in response to changes in pH, making it useful in various laboratory and industrial applications. Methyl Red is commonly used in microbiology to differentiate between bacteria that produce stable acids and those that do not. It is also used in the textile industry as a dye and in the production of plastics and pharmaceuticals. However, it is important to handle and dispose of 3,3-DIMETHYL-1-(2-CARBOXYPHENYL)TRIAZENE with care, as it is classified as a hazardous substance due to its toxic and potentially carcinogenic properties.

InChI:InChI=1/C9H11N3O2/c1-12(2)11-10-8-6-4-3-5-7(8)9(13)14/h3-6H,1-2H3,(H,13,14)/b11-10+

20119-28-2 Relevant articles

Aryne formation from 1-(3′-Carboxyaryl)-3,3-dim ethyl trianzenes

Christopher Buxton,Heaney, Harry

, p. 3929 - 3938 (1995)

A study of the decomposition of 1-(2′-ca...

Reaction of benzyne with formamides and acetylimidazole

Okuma, Kentaro,Nojima, Akiko,Nakamura, Yuki,Matsunaga, Nahoko,Nagahora, Noriyoshi,Shioji, Kosei

experimental part, p. 328 - 332 (2011/05/14)

The reaction of DMF with o-trimethylsily...

Waste-Free Quantitative Gas/Solid Diazotation Using Nitrogen Dioxide and Triazene Synthesis, Both Avoiding Liquid Phases

Kaupp, Gerd,Herrmann, Andreas

, p. 256 - 260 (2007/10/03)

Solid diazonium nitrates (2a-j) are quan...

AFM in organic solid state reactions

Kaupp, Gerd,Schmeyers, Jens,Haak, Michael,Marquardt, Thorsten,Herrmann, Andreas

, p. 315 - 317 (2007/10/03)

Organic solid-state reactions are probed...

20119-28-2 Process route

benzenedizolium-2-carboxylate
1608-42-0

benzenedizolium-2-carboxylate

dimethyl amine
124-40-3

dimethyl amine

2-(3,3-dimethyltriazen-1-yl)benzoic acid
20119-28-2

2-(3,3-dimethyltriazen-1-yl)benzoic acid

Conditions
Conditions Yield
In tetrahydrofuran; Reflux;
100%
2-carboxybenzene diazonium chloride
4661-46-5

2-carboxybenzene diazonium chloride

dimethyl amine
124-40-3

dimethyl amine

2-(3,3-dimethyltriazen-1-yl)benzoic acid
20119-28-2

2-(3,3-dimethyltriazen-1-yl)benzoic acid

Conditions
Conditions Yield
In dichloromethane; at 0 ℃; for 1h; Yield given;

20119-28-2 Upstream products

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    124-40-3

    dimethyl amine

  • 4661-46-5
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    2-carboxybenzene diazonium chloride

  • 1608-42-0
    1608-42-0

    benzenedizolium-2-carboxylate

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