Trichloroisocyanuric acid Basic Product Information

Product Name	Trichloroisocyanuric acid	CAS	87-90-1
Synonyms	1,3, 5-Trichloro-s-triazinetrione;s-Triazine-2,4,6(1H,3H,5H)-trione, 1,3,5-trichloro-;Symclosen;ACL 85;1,3,5-Trichloro-s-triazinetrione;Trichloroisocyanic acid;1,3,5-Trichloro-s-triazine-2,4,6(1H,3H,5H)-trione;EPA Pesticide Chemical Code 081405;Trichloroisocyanurate;Trichlorinated isocyanuric acid;1,3,5-Trichloroisocyanuric acid;Trichloro-s-triazinetrione, dry;Trichloro-s-triazine-2,4,6(1H,3H,5H)-trione;N,N,N;1,3, 5-Triazine-2,4,6(1H,3H,5H)-trione, 1,3,5-trichloro-;Trichlorocyanuric acid;Sincloseno [INN-Spanish];1,3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3,5- trichloro-;Chloreal;Neochlor 90;1,3,5-Trichloro-2,4, 6-trioxohexahydro-s-triazine;1,3,5-trichloro-1,3,5-triazine-2,4,6(1H,3H,5H)-trione;Fi Clor 91;Trichloro-s-triazinetrione;Isocyanuric chloride;1,3, 5-Triazine-2,4,6 (1H,3H,5H)-trione, 1,3,5-trichloro-;Trichlorisocyanursaeure;CBD 90;ACL 90;Fichlor 91;Hi-Lite 90G;1,3,5-Triazine-2,4,6(1H,3H,5H)-trione, 1,3,5-trichloro-;N,N,N-Trichloroisocyanuric acid;1,3,5-trichloro-1,3,5-triazinane-2,4,6-trione;Symclosenum [INN-Latin];1,3, 5-Trichloro-s-triazine-2,4,6(1H,3H,5H)-trione;s-Triazine-2,4,6 (1H,3H,5H)-trione, 1,3,5-trichloro-;Kyselina trichloisokyanurova;Slow Dissolving Chlorine Tablets;1,3,5-Trichloro-2,4,6-trioxohexahydro-s-triazine;TCCA;Trichloroisocyanuric Acid(TCCA);TCCA (Trichloro Isocyanuric Acid);	Molecular Formula	C3Cl3N3O3
EINECS Number	201-782-8	Molecular Structure
Appearance	Light Yellow Powder
Purity	Effective chlorine content: ≥90%
Supply Ability

Trichloroisocyanuric acid Quality documents

Trichloroisocyanuric acid Appearance/Package/Shipping/Storage

package

storage condition

Store in cool & dry place,Keep away from strong light and heat

Trichloroisocyanuric acid Application

Trichloroisocyanuric acid literature

Preparation method of omeprazole midbody

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Paragraph 0069-0075, (2019/10/22)

The invention relates to a preparation method of 2-chloromethyl-3,5-dimethyl-4-methoxypyridine shown in a chemical structural formula I. The method is characterized by comprising the steps of a catalytic hydrogenation reaction, wherein Raney nickel or Pd/C is selected as a catalyst; a chlorination reaction, wherein YCln is selected from N-chloroacetamides or N-chlorosuccinimide or 1,3-dichloro-5,5-dimethylhydantoin or dichlord isocyanurice acid or symclosene; n is selected from 3 or 2 or 1; m is selected from 0 or 1 or 2.

Preparation method of 2-chloro-5-chloromethylpyridine

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Paragraph 0097-0117, (2017/07/19)

The invention relates to the field of chemical synthesis, particularly a preparation method of 2-chloro-5-chloromethylpyridine. The preparation method comprises the following step: carrying out cyclization reaction on 2-chloro-2-chloromethyl-4-cyanobutyraldehyde and cyanuric chloride to obtain the 2-chloro-5-chloromethylpyridine. The preparation method provided by the invention has the advantages of low production cost, high product quality, high yield and the like. Besides, the byproduct sodium cyanurate of the preparation method can be treated to prepare thetrichloroisocyanuric acid superior product, thereby further enhancing the economic benefits.

Preparation method of trichloroisocyanuric acid

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Paragraph 0034-0069, (2017/10/26)

The invention discloses a preparation method of trichloroisocyanuric acid and belongs to the field of production of chemical products. The preparation method of the trichloroisocyanuric acid comprises the following steps: selecting cyanuric acid and dichlorine monoxide as raw materials, and selecting water as a solvent to carry out chlorination reaction, so as to obtain target product trichloroisocyanuric acid. According to the preparation method of the trichloroisocyanuric acid, disclosed by the invention, the water is selected as the solvent, so an obtained product is insoluble in water; after the reaction is finished, the operation of separating the product is simple, and technical essentials are easily grasped; moreover, a mother solution can be recycled without undergoing treatment, and the trichloroisocyanuric acid is clean and pollution-free and benefits to reducing the production cost.

Method for preparing trichloroisocyanuric acid by utilizing solvent process

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Paragraph 0007; 0008; 0009; 0010; 0011, (2017/05/12)

The invention belongs to the technical field of preparation of trichloroisocyanuric acid and discloses a method for preparing trichloroisocyanuric acid by utilizing a solvent process. According to the technical scheme, the method for preparing the trichloroisocyanuric acid by utilizing the solvent process comprises the following steps: by taking a solvent as a reaction medium, adding trisodium cyanurate into the solvent, introducing chlorine, carrying out chlorination reaction at the reaction temperature of 0-50 DEG C, carrying out centrifugal separation on reacted materials to obtain sodium chloride, distilling centrifugal mother liquid in a reaction kettle, condensing and recycling the solvent, wherein the obtained concentrate is namely the trichloroisocyanuric acid. The method disclosed by the invention has the advantages that the solvent is taken as the medium, water does not need to be used in a reaction process, water resource is greatly saved, and energy consumption in aftertreatment of mother liquor in an aqueous phase process is greatly reduced.

Trichloroisocyanuric acid Upstream and downstream

87-90-1 Upstream product

• 108-80-5

  cyanuric acid 

• 26231-96-9

  N'-carbonyl-N,N-dichloro-urea 

• 108-80-5

  isocyanuric acid 

• 17497-85-7

  1,3,5-tribromo-1,3,5-triazinane-2,4,6-trione 

• 13858-09-8

  chlorine isocyanate 

• 7681-49-4

  sodium fluoride 

• 7782-50-5

  chlorine 

• 27694-85-5

  triiodoisocyanuric acid 

87-90-1 Downstream Products

• 3019-71-4

  Trichloroacetyl isocyanate 

• 556-99-0

  triuret 

• 124-04-9

  Adipic acid 

• 64-18-6

  formic acid 

• 64-19-7

  acetic acid 

• 108-80-5

  cyanuric acid 

• 2782-57-2

  1,3-dichloro-[1,3,5]triazinane-2,4,6-trione 

• 7664-93-9

  sulfuric acid 

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