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Home > Encyclopedia > Thiazolium, 3-methyl-2-[2-(1-methyl-2-phenyl-1H-indol-3-yl)diazenyl]-, chloride (1:1)

Thiazolium, 3-methyl-2-[2-(1-methyl-2-phenyl-1H-indol-3-yl)diazenyl]-, chloride (1:1)

Thiazolium, 3-methyl-2-[2-(1-methyl-2-phenyl-1H-indol-3-yl)diazenyl]-, chloride (1:1) structure

Thiazolium, 3-methyl-2-[2-(1-methyl-2-phenyl-1H-indol-3-yl)diazenyl]-, chloride (1:1) 

structure
  • CAS No:

    42373-04-6

  • Formula:

    C19H17N4S.Cl

  • Chemical Name:

    Thiazolium, 3-methyl-2-[2-(1-methyl-2-phenyl-1H-indol-3-yl)diazenyl]-, chloride (1:1)

  • Synonyms:

    Thiazolium,3-methyl-2-[2-(1-methyl-2-phenyl-1H-indol-3-yl)diazenyl]-,chloride (1:1);Thiazolium,3-methyl-2-[(1-methyl-2-phenyl-1H-indol-3-yl)azo]-,chloride;121181-49-5;11075-22-2;68893-90-3

  • Categories:

    Dyes and Pigments  >  Dye

Thiazolium, 3-methyl-2-[2-(1-methyl-2-phenyl-1H-indol-3-yl)diazenyl]-, chloride (1:1) Basic Attributes

368.88

368.08600

255-785-4

DTXSID0030900

Characteristics

61.77000

2.15070

dark red powder

Safety Information

NONH for all modes of transport

3

36/37/38

26-36

XJ7050330

Xi

P261-P305 + P351 + P338

H315-H319-H335

|Warning|H315 (90.48%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 43 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

Basacryl Red GL

Thiazolium, 3-methyl-2-[2-(1-methyl-2-phenyl-1H-indol-3-yl)diazenyl]-, chloride (1:1) Use and Manufacturing

Methods of Manufacturing

Using 2-aminothiazole and N-methyl-2-phenylindole as the main raw materials, first diazotize 2-aminothiazole with sodium nitrite and sulfuric acid at -5- -4℃, and then diazotize it with N-methyl -2-phenylindole is coupled, finally methylated with dimethyl sulfate, filtered, washed, and dried to obtain the finished product. . Add 408L of water, 330kg of sulfuric acid (93%) to the reaction pot, cool to 3°C, add 36kg of 2-aminothiazole (100%), continue to cool to -3- -4°C, add dropwise sodium nitrite solution (containing Sodium nitrate 30kg), add it within 1.5-2h, and keep it for 40min. Add 600L of water and 1.5t of ice to another reaction pot, and then suck in the above diazotized material, cool to 0-3℃, and slowly add the prepared N-methyl-2-phenylindole solution [from 300L of water , 6kg emulsifier OP, 69kg N-methyl-2-phenylindole and 555kg sulfuric acid (93%)], add it within 40-60min, and the reaction will reach the end. Then it was heated to 23°C and filtered. Add 75L of water and the above-mentioned dye matrix filter cake to the reaction pot, adjust the volume to 420L, add 27kg of magnesium oxide below 26°C, and add 57kg of dimethyl sulfate below 15°C, react at 33-35°C for 3h, and heat up to 90 ℃, adjust the volume to 2200L, filter at 60℃, salt out the filtrate, filter and dry to obtain the finished product.

Uses

Mainly used for dyeing acrylic loose fibers, fiber strips and acrylic fleece

Thiazolium, 3-methyl-2-[2-(1-methyl-2-phenyl-1H-indol-3-yl)diazenyl]-, chloride (1:1): ACTIVE

Computed Properties

Molecular Weight:368.9
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:368.0862454
Monoisotopic Mass:368.0862454
Topological Polar Surface Area:61.8
Heavy Atom Count:25
Complexity:451
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

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