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87-90-1 Usage

Chemical Description

Different sources of media describe the Chemical Description of 87-90-1 differently. You can refer to the following data:
1. Trichloroisocyanuric acid is a chlorinated derivative of isocyanuric acid.
2. Trichloroisocyanuric acid is a white crystalline powder that is commonly used as a disinfectant and bleaching agent.

Bactericidal and Disinfection effect

Trichloroisocyanuric acid (TCCA) is a strong oxidant and chlorinating agent which has efficient, broad-spectrum, and safe disinfection effects. It has the strongest bactericidal activity among chlorinated isocyanuric acid products against bacteria, viruses, fungi, mold, Vibrio cholerae, Bacillus. It also has certain inhibitory effect on coccidia oocysts and thus can used in the disinfection in the environment, drinking water, fruits and vegetables, livestock feeders, fish ponds and silkworm rooms. The application method is using powder for the preparation of 4-6 mg/kg concentrations for the disinfection of drinking water and using a solution of concentration of 200-400 mg/kg for environmental disinfection and utensils disinfection. TCCA has various effects including killing algae, deodorant, and water purification as well as bleaching. It has a stronger and better bactericidal and bleaching effect than sodium dichloroisocyanurate and thus being widely used in the sterilization treatment of washing bleacher of cotton and hemp fiber fabric, wool shrink proofing agents, rubber chlorination, and oil drilling mud and sewage, disinfection of battery materials, disinfection of swimming pool, disinfection of drinking water, treatment of industrial wastewater and sewage, food processing industry, food hygiene industry, aquaculture, daily chemical industry, hospitals, nurseries, epidemic prevention, waste disposal, hotels, restaurants and natural disasters, large-scale disinfection and sterilization after man-made disaster. Instructions: 1. swimming pool disinfection: calculate the usage according to 2-3g/m3; take effect for 30-60 minutes. 2. Public places and ground disinfection: use 1500-3000-fold diluted water solution for spraying and wiping for 30 minutes. Infectious disease epidemic area, use 150-200-fold aqueous diluted water solution for spray disinfection. 3. disinfection of white clothing and blankets: apply 2000-3000 fold diluted solution for clean items; soak for 10 minutes; for seriously polluted items, diluted 500 times, soak for 20 minutes. 4. disinfection of bathroom and toilet scrub; use 300-fold diluted solution for reaction of 30 minutes. 5. sterilization of non-metallic medical equipment: use 500-1000 times diluted solution for soak of 30 minutes; disinfection of apparatus with pus and blood; apply 100-fold diluted water solution for reaction of 30 minutes. 6. disinfection of non-metallic tableware: use 500-1000 times diluted water solution for reaction of 30 minutes.

Chemical Properties

Different sources of media describe the Chemical Properties of 87-90-1 differently. You can refer to the following data:
1. TCCA has an excellent bactericidal property and is a new generation of broad-spectrum, high efficiency, low-toxicity fungicides, bleacher and anti-shrinking agent. It is mainly used in the disinfection and sterilization of drinking water, industrial water recycling, swimming pool, restaurants, hotels, public places, homes, hospitals, eggs and prevention of fish diseases. It has a killing effect on almost all fungi, bacteria, viruses, and spores. It is safe and convenient to use. This product can also be widely used in food, dairy, rice seed processing, fruit preservation, fiber bleaching, wool shrink, daily chemical decolorization, wood mold paper making, rubber oxidation and battery materials. The above information is edited by the lookchem of Dai Xiongfeng.
2. white to light yellow crystal powde

Uses

Different sources of media describe the Uses of 87-90-1 differently. You can refer to the following data:
1. The product has a strong sterilization, bleaching effect. It is widely used as the high-efficiency disinfectant in civilian health, livestock breeding and plant protection. It can also be used as the washing bleacher of cotton and hemp fiber fabric, wool shrink proofing agents; it can also be used for rubber chlorination, battery materials, organic synthesis industry and the bleach of dry laundry. It is used for the sterilization and disinfection of various kinds of water such as drinking water, swimming pool water, industrial circulating water, and sewage. It is an anti-clotting drug.
2. Trichloroisocyanuric Acid is a disinfectant and anti-bacterial. It can also be used in the synthesis of napthols.
3. Chlorinating agent, disinfectant, industrial deodorant. In household cleansers. In removing oil and protein in stainless steel. In nonshrink treatment for wool. Oxidant and chlorinating reagent in organic synthesis.

Acute toxicity

oral: rat LD50: 406 mg/kg

Irritation data

skin: rabbit 500 mg/24 hours: moderate; Eyes-rabbit 50 micrograms/24 hours and severe.

Explosiveness and Hazardous characteristics

being mixed with ammonium salt, ammonia, urea can generate explosive nitrogen trichloride.

Flammability and hazard characteristics

it is flammable in case of organic substance; it can generate toxic nitrogen trichloride upon wet and heating.

Storage characteristics

Treasury: ventilation, low-temperature and dry; it should be stored separately from fuel, organic matter, and oxides.

Fire extinguishing agent

Plenty of water

General Description

A white slightly hygroscopic crystalline powder or lump solid with a mild chlorine-like odor. Said to have 85 percent available chlorine. Decomposes at 225°C. Moderately toxic by ingestion. May irritate skin and eyes. Active ingredient in household dry bleaches. Used in swimming pools as a disinfectant .

Air & Water Reactions

Slightly hygroscopic [Hawley]. Slightly soluble in water. May react with water releasing gaseous chlorine. If mixed with a small amount of water, the concentrated solution (with pH at about 2.0) may explode due to the evolution of unstable nitrogen trichloride. (explanation in Bretherick 5th ed.)

Reactivity Profile

TRICHLORO-S-TRIAZINETRIONE, [DRY, CONTAINING > 39% AVAILABLE CHLORINE] may react vigorously with ammonium compounds or hydrated salts. Prolonged exposure to heat may result in the vigorous decomposition with the rupture of containers. Accelerates the burning of combustible materials [AAR 1991]. May reactwith alcohols to yield alkyl hypochlorites that decompose in the cold and explode on exposure to sunlight or heat. Hypochlorites of tertiary alcohols are less unstable than those of secondary or primary alcohols [NFPA 491 M. 1991].

Health Hazard

Different sources of media describe the Health Hazard of 87-90-1 differently. You can refer to the following data:
1. Inhalation causes sneezing and coughing. Contact with dust causes moderate irritation of eyes and itching and redness of skin. Ingestion causes burns of mouth and stomach.
2. Moderately toxic by ingestion; causes lethargy, weakness, bleeding from stomach, andulceration; ingestion of very large quantities,probably within the range 150–100 g, maycause delayed death; as a strong oxidizer,the toxic properties of this substance showmany similarities to other powerful oxidants;injurious to liver and kidney, causing inflammation of gastrointestinal tract, liver discoloration, and kidney hyperemia as indicatefrom autopsy (Sax and Lewis 1995); the dermal toxicity is very low although an irritantto skin; irritation in rabbit’s eye form a 50mg dose in 24 hours was found to be severe.LD50 oral (rat): 406 mg/kg.

Safety Profile

Moderately toxic to humans and experimentally by ingestion. Mildly toxic experimentally by skin contact. Human systemic effects by ingestion: ulceration or bleeding from stomach. A severe skin and eye irritant. Toxicity symptoms include emaciation, lethargy, weakness, and delayed death. Autopsy shows inflammation of gastrointestinal tract, liver discoloration, and kidney hyperemia. A powerful oxidizer. Forms an explosive product with cyanuric acid + sodmm hydroxide. Potentially violent reaction with combustible materials. When heated to decomposition it emits very toxic fumes of Cland NOx. Used to chlorinate swimming pools.

Check Digit Verification of cas no

The CAS Registry Mumber 87-90-1 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87-90:
(4*8)+(3*7)+(2*9)+(1*0)=71
71 % 10 = 1
So 87-90-1 is a valid CAS Registry Number.
InChI:InChI=1/C3Cl3N3O3/c4-7-1(10)8(5)3(12)9(6)2(7)11

87-90-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (T0620)  Trichloroisocyanuric Acid  >95.0%(T)

  • 87-90-1

  • 25g

  • 155.00CNY

  • Detail
  • TCI America

  • (T0620)  Trichloroisocyanuric Acid  >95.0%(T)

  • 87-90-1

  • 500g

  • 390.00CNY

  • Detail
  • Alfa Aesar

  • (B23906)  Trichloroisocyanuric acid, 90+%   

  • 87-90-1

  • 100g

  • 197.0CNY

  • Detail
  • Alfa Aesar

  • (B23906)  Trichloroisocyanuric acid, 90+%   

  • 87-90-1

  • 500g

  • 468.0CNY

  • Detail
  • Alfa Aesar

  • (B23906)  Trichloroisocyanuric acid, 90+%   

  • 87-90-1

  • 2500g

  • 1858.0CNY

  • Detail
  • Aldrich

  • (176125)  Trichloroisocyanuricacid  

  • 87-90-1

  • 176125-50G

  • 259.74CNY

  • Detail
  • Aldrich

  • (176125)  Trichloroisocyanuricacid  

  • 87-90-1

  • 176125-250G

  • 439.92CNY

  • Detail
  • Aldrich

  • (176125)  Trichloroisocyanuricacid  

  • 87-90-1

  • 176125-1KG

  • 670.41CNY

  • Detail
  • Sigma-Aldrich

  • (91220)  Trichloroisocyanuricacid  technical, ≥95% (CHN)

  • 87-90-1

  • 91220-100G

  • 226.98CNY

  • Detail
  • Sigma-Aldrich

  • (91220)  Trichloroisocyanuricacid  technical, ≥95% (CHN)

  • 87-90-1

  • 91220-500G

  • 746.46CNY

  • Detail

87-90-1SDS

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

1.2 Other means of identification

Product number -
Other names 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione, 1,3,5-trichloro-

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:87-90-1 SDS

87-90-1Synthetic route

cyanuric acid
108-80-5

cyanuric acid

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

Conditions
ConditionsYield
With chlorine; calcium carbonate In water100%
With hypochlorous anhydride In water at 25℃; for 6h; pH=3.5; pH-value; Temperature; Large scale;98%
With sodium hydroxide; chlorine unter der Einwirkung von UV-Licht;
With potassium hydroxide; chlorine unter der Einwirkung von UV-LIcht;
sodium cyanurate
3047-33-4

sodium cyanurate

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

Conditions
ConditionsYield
With chlorine In toluene at 30 - 40℃; pH=3 - 3.5; Solvent; pH-value; Temperature; Large scale;93.65%
With chlorine at 10 - 23℃; Temperature; Flow reactor; Large scale;
With chlorine; sodium hydroxide In methanol; water at 5 - 65℃; for 0.166667h; pH=2.5 - 3; Solvent; Temperature; Reagent/catalyst;12.98 g
N'-carbonyl-N,N-dichloro-urea
26231-96-9

N'-carbonyl-N,N-dichloro-urea

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

isocyanuric acid
108-80-5

isocyanuric acid

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

Conditions
ConditionsYield
With potassium hydroxide; chlorine
With chlorine; calcium hydroxide In water at 40 - 50℃; pH=4;
cyanuric acid
108-80-5

cyanuric acid

A

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

B

1,3-dichloro-[1,3,5]triazinane-2,4,6-trione
2782-57-2

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

C

chloro-isocyanuric acid

chloro-isocyanuric acid

Conditions
ConditionsYield
In water reactn. with single positive charged Cl;
In water reactn. with single positive charged Cl;
1,3,5-tribromo-1,3,5-triazinane-2,4,6-trione
17497-85-7

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

A

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

B

bromine chloride
13863-41-7

bromine chloride

Conditions
ConditionsYield
90°C;A >99
B n/a
chlorine isocyanate
13858-09-8

chlorine isocyanate

sodium fluoride

sodium fluoride

A

Carbonyl fluoride
353-50-4

Carbonyl fluoride

B

carbon monoxide
201230-82-2

carbon monoxide

C

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

Conditions
ConditionsYield
byproducts: NaCl, SiF4; with dry NaF, 300°C;
chlorine isocyanate
13858-09-8

chlorine isocyanate

A

nitrogen trichloride
10025-85-1

nitrogen trichloride

B

carbon dioxide
124-38-9

carbon dioxide

C

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

D

1,3-dichloro-[1,3,5]triazinane-2,4,6-trione
2782-57-2

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

E

1,3-dichloro-1,3-diazetidine-2,4-dione
24604-62-4

1,3-dichloro-1,3-diazetidine-2,4-dione

Conditions
ConditionsYield
slow react. above the melting point, fast at room temp., dichlorouretidindione formed by vac. sublimation (50.degrre.C, 0.1 Torr), di- and trichlocyanuric acid yielded by 48h sublimation of the residue at 95-160°C;
chlorine isocyanate
13858-09-8

chlorine isocyanate

A

N'-carbonyl-N,N-dichloro-urea
26231-96-9

N'-carbonyl-N,N-dichloro-urea

B

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

Conditions
ConditionsYield
With alkali fluorides in presence of anhyd. alkali fluorides, 50 Torr, room temp.;
cyanuric acid
108-80-5

cyanuric acid

chlorine
7782-50-5

chlorine

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

Conditions
ConditionsYield
vigorous stirring, 0°C; filtering, drying, sublimated in vac. at 170°C;
vigorous stirring, 0°C; filtering, drying, sublimated in vac. at 170°C;
triiodoisocyanuric acid
27694-85-5

triiodoisocyanuric acid

chlorine
7782-50-5

chlorine

A

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

B

iodine
7553-56-2

iodine

Conditions
ConditionsYield
room temp.;
1,3-dichloro-1,3-diazetidine-2,4-dione
24604-62-4

1,3-dichloro-1,3-diazetidine-2,4-dione

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

Conditions
ConditionsYield
above the melting point at atmospheric pressure;
In acetonitrile
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

6-bromo-7-fluoro-4-{[(1S)-1-(tetrahydro-2H-pyran-4-yl)ethyl]amino}-3-quinolinecarboxamide

6-bromo-7-fluoro-4-{[(1S)-1-(tetrahydro-2H-pyran-4-yl)ethyl]amino}-3-quinolinecarboxamide

(S)-8-bromo-7-fluoro-1-(1-(tetrahydro-2H-pyran-4-yl)ethyl)-1H-imidazo[4,5-c]quinolin-2(3H)-one

(S)-8-bromo-7-fluoro-1-(1-(tetrahydro-2H-pyran-4-yl)ethyl)-1H-imidazo[4,5-c]quinolin-2(3H)-one

Conditions
ConditionsYield
With 1,8-diazabicyclo[5.4.0]undec-7-ene In methanol at 0 - 20℃; for 0.333333h; Inert atmosphere;100%
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

Benzyl 4-hydroxybenzoate
94-18-8

Benzyl 4-hydroxybenzoate

benzyl 4-formylbenzoate
78767-55-2

benzyl 4-formylbenzoate

Conditions
ConditionsYield
With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sodium hydrogencarbonate In dichloromethane for 0.0833333h;99%
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

6-bromo-4-[(cis-3-methoxycyclobutyl)amino]quinoline-3-carboxamide

6-bromo-4-[(cis-3-methoxycyclobutyl)amino]quinoline-3-carboxamide

8-bromo-1-(cis-3-methoxycyclobutyl)-3H-imidazo[4,5-c]quinolin-2-one

8-bromo-1-(cis-3-methoxycyclobutyl)-3H-imidazo[4,5-c]quinolin-2-one

Conditions
ConditionsYield
With 1,8-diazabicyclo[5.4.0]undec-7-ene In methanol at 0 - 20℃; for 18h; Inert atmosphere;99%
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

2-(2-((trifluoromethyl)thio)phenyl)pyridine
1584705-57-6

2-(2-((trifluoromethyl)thio)phenyl)pyridine

2-(2-((trifluoromethyl)sulfinyl)phenyl)pyridine

2-(2-((trifluoromethyl)sulfinyl)phenyl)pyridine

Conditions
ConditionsYield
Stage #1: 2-(2-((trifluoromethyl)thio)phenyl)pyridine In dichloromethane; acetonitrile at 20℃; for 0.0833333h; Schlenk technique; Inert atmosphere;
Stage #2: trichloroisocyanuric acid In dichloromethane; acetonitrile at 20℃; for 1h; Schlenk technique; Inert atmosphere;
99%
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

6-bromo-7-fluoro-4-(tetrahydro-2H-pyran-4-ylamino)quinoline-3-carboxamide

6-bromo-7-fluoro-4-(tetrahydro-2H-pyran-4-ylamino)quinoline-3-carboxamide

8-bromo-7-fluoro-1-(oxan-4-yl)-3H-imidazo[4,5-c]quinolin-2-one

8-bromo-7-fluoro-1-(oxan-4-yl)-3H-imidazo[4,5-c]quinolin-2-one

Conditions
ConditionsYield
With 1,8-diazabicyclo[5.4.0]undec-7-ene In methanol at 0 - 20℃; for 0.25h; Inert atmosphere;98%
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

1-(4-bromophenyl)-1H-imidazole
10040-96-7

1-(4-bromophenyl)-1H-imidazole

2-hydroxy-4,6-bis(4-bromophenylimidazolium)-1,3,5-triazinide dichloride

2-hydroxy-4,6-bis(4-bromophenylimidazolium)-1,3,5-triazinide dichloride

Conditions
ConditionsYield
In acetonitrile at 0 - 110℃; for 20.5h;96%
2,3,5-trimethyl-pyridine
695-98-7

2,3,5-trimethyl-pyridine

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

benzamide
55-21-0

benzamide

2-chloromethyl-3,5-dimethyl-4-nitro-pyridine N-oxide
142885-89-0

2-chloromethyl-3,5-dimethyl-4-nitro-pyridine N-oxide

Conditions
ConditionsYield
With sodium hydroxide In water93%
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

dicloroiodoisocyanuric acid
1376143-54-2

dicloroiodoisocyanuric acid

Conditions
ConditionsYield
Stage #1: trichloroisocyanuric acid With iodine at 170℃; for 18h;
Stage #2: at 220℃; for 24h;
93%
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

thiophenol
108-98-5

thiophenol

A

isocyanuric acid
108-80-5

isocyanuric acid

B

diphenyldisulfane
882-33-7

diphenyldisulfane

Conditions
ConditionsYield
With pyridine; water; benzoic acid In dichloromethane; acetonitrile at 40℃;A n/a
B 91%
1-(Trimethylsilyloxy)cyclohexene
6651-36-1

1-(Trimethylsilyloxy)cyclohexene

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

A

silyl enol ether

silyl enol ether

B

2-Chlorocyclohexanone
822-87-7

2-Chlorocyclohexanone

Conditions
ConditionsYield
With hydrogenchloride In diethyl ether; ethyl acetateA n/a
B 91%
With hydrogenchloride In diethyl ether; ethyl acetateA n/a
B 91%
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

triiodoisocyanuric acid
27694-85-5

triiodoisocyanuric acid

Conditions
ConditionsYield
With iodine at 180 - 230℃; for 72h;90%
With iodine at 180 - 230℃; for 72h; Sealed tube;90%
With iodine Sealed tube; Heating;
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

para-thiocresol
106-45-6

para-thiocresol

A

di(p-tolyl) disulfide
103-19-5

di(p-tolyl) disulfide

B

isocyanuric acid
108-80-5

isocyanuric acid

Conditions
ConditionsYield
With pyridine; water; benzoic acid In dichloromethane; acetonitrile at 40℃;A 89%
B n/a
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

2-(3-hydroxypropoxy)ethyl nitrate
1321459-27-1

2-(3-hydroxypropoxy)ethyl nitrate

3-(2-(nitrooxy)ethoxy)propanoic acid
1321459-22-6

3-(2-(nitrooxy)ethoxy)propanoic acid

Conditions
ConditionsYield
With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sodium hydrogencarbonate; sodium bromide In acetone at 0 - 20℃; for 3h;89%
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

potassium-2-phenyl-3-(trifluoro-l4-boraneyl)-1,2-dihydrobenzo[e][1,2]-azaborinine

potassium-2-phenyl-3-(trifluoro-l4-boraneyl)-1,2-dihydrobenzo[e][1,2]-azaborinine

3-chloro-2-phenyl-1,2-dihydrobenzo[e][1,2]azaborinine

3-chloro-2-phenyl-1,2-dihydrobenzo[e][1,2]azaborinine

Conditions
ConditionsYield
In diethyl ether; water at 20℃; Inert atmosphere;89%
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

diphenylgermane
1675-58-7

diphenylgermane

diphenylchlorogermane
7366-23-6

diphenylchlorogermane

Conditions
ConditionsYield
In tetrahydrofuran at -80 - 20℃; Inert atmosphere; Schlenk technique;89%
2-(4-nitro-phenyl)-4,4-dimethyl-5-methylene-4,5-dihydrooxazole
214420-92-5

2-(4-nitro-phenyl)-4,4-dimethyl-5-methylene-4,5-dihydrooxazole

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

N-(1-chloro-3-methyl-2-oxobut-3-yl)-4-nitrobenzamide

N-(1-chloro-3-methyl-2-oxobut-3-yl)-4-nitrobenzamide

Conditions
ConditionsYield
With hydrogenchloride In hexane; water; ethyl acetate88%
With hydrogenchloride In hexane; water; ethyl acetate88%
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

(1-naphthyl)2GeH2

(1-naphthyl)2GeH2

1-naphthylGe(Cl)H2

1-naphthylGe(Cl)H2

Conditions
ConditionsYield
In tetrahydrofuran at -80 - 20℃; Inert atmosphere; Schlenk technique;88%
2-(3,5-dichloro-4-methylphenyl)-4-ethyl-4-methyl-5-methyleneoxazoline
209809-70-1

2-(3,5-dichloro-4-methylphenyl)-4-ethyl-4-methyl-5-methyleneoxazoline

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

zoxamide
156052-68-5

zoxamide

Conditions
ConditionsYield
With hydrogenchloride In water; ethyl acetate87%
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

6-(pyridin-3-yl)-4-(tetrahydro-2H-pyran-4-ylamino)quinoline-3-carboxamide

6-(pyridin-3-yl)-4-(tetrahydro-2H-pyran-4-ylamino)quinoline-3-carboxamide

8-(pyridin-3-yl)-1-(tetrahydro-2H-pyran-4-yl)-1H-imidazo[4,5-c]quinolin-2(3H)-one

8-(pyridin-3-yl)-1-(tetrahydro-2H-pyran-4-yl)-1H-imidazo[4,5-c]quinolin-2(3H)-one

Conditions
ConditionsYield
With 1,8-diazabicyclo[5.4.0]undec-7-ene In methanol at 0 - 20℃; for 0.5h; Inert atmosphere;87%
3,7-dimethyl-2E,6-octadien-1-yl acetate
105-87-3

3,7-dimethyl-2E,6-octadien-1-yl acetate

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

A

cyanuric acid
108-80-5

cyanuric acid

B

6-chloro-3,7-dimethyl-2,7-octadiene-1-acetate

6-chloro-3,7-dimethyl-2,7-octadiene-1-acetate

Conditions
ConditionsYield
In hexaneA n/a
B 86%
In hexaneA n/a
B 86%
3,7-dimethyl-2E,6-octadien-1-yl acetate
105-87-3

3,7-dimethyl-2E,6-octadien-1-yl acetate

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

A

cyanuric acid
108-80-5

cyanuric acid

B

6-chloro-3,7-dimethyl-2,7-octadien-1-acetate

6-chloro-3,7-dimethyl-2,7-octadien-1-acetate

Conditions
ConditionsYield
In hexaneA n/a
B 86%
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

tert-butyl (2R,4R)-2-(5-fluoropyridin-3-yl)-4-hydroxypyrrolidine-1-carboxylate

tert-butyl (2R,4R)-2-(5-fluoropyridin-3-yl)-4-hydroxypyrrolidine-1-carboxylate

tert-butyl (R)-2-(5-fluoropyridin-3-yl)-4-oxopyrrolidine-1-carboxylate

tert-butyl (R)-2-(5-fluoropyridin-3-yl)-4-oxopyrrolidine-1-carboxylate

Conditions
ConditionsYield
With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical at -10 - 25℃; for 1.25h;85.32%
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

7-fluoro-4-((trans-3-methoxycyclobutyl)amino)-6-(6-(methoxymethyl)pyridin-3-yl)quinoline-3-carboxamide

7-fluoro-4-((trans-3-methoxycyclobutyl)amino)-6-(6-(methoxymethyl)pyridin-3-yl)quinoline-3-carboxamide

7-fluoro-1-(trans-3-methoxycyclobutyl)-8-(6-(methoxymethyl)pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-2(3H)-one

7-fluoro-1-(trans-3-methoxycyclobutyl)-8-(6-(methoxymethyl)pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-2(3H)-one

Conditions
ConditionsYield
With 1,8-diazabicyclo[5.4.0]undec-7-ene In methanol at 0 - 20℃; Inert atmosphere;85%
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

dibutylgermane
29823-30-1

dibutylgermane

di-n-butylchlorogermane
14275-42-4

di-n-butylchlorogermane

Conditions
ConditionsYield
In tetrahydrofuran at -80 - 20℃; Inert atmosphere; Schlenk technique;85%
4-Methoxybenzenethiol
696-63-9

4-Methoxybenzenethiol

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

A

4,4'-dimethoxyphenyl disulfide
5335-87-5

4,4'-dimethoxyphenyl disulfide

B

isocyanuric acid
108-80-5

isocyanuric acid

Conditions
ConditionsYield
With pyridine; water; benzoic acid In dichloromethane; acetonitrile at 40℃;A 83%
B n/a
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

benzamide
55-21-0

benzamide

4-chloro-2,3,5-trimethylpyridine 1-oxide
109371-20-2

4-chloro-2,3,5-trimethylpyridine 1-oxide

4-chloro-2-chloromethyl-3,5-dimethylpyridine N-oxide

4-chloro-2-chloromethyl-3,5-dimethylpyridine N-oxide

Conditions
ConditionsYield
In dichloromethane; chloroform; water83%
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

triethyl phosphite
122-52-1

triethyl phosphite

hexahydro-1,3,5-tris(diethoxyphosphoryl)-1,3,5-triazine-2,4,6-trione

hexahydro-1,3,5-tris(diethoxyphosphoryl)-1,3,5-triazine-2,4,6-trione

Conditions
ConditionsYield
at 100 - 110℃; for 12h;82%
at 90℃;78%
In benzene72%
trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

((2S,3R)-2,2-dimethyl-5-((4'R,5'S)-2',2',5'-trimethyl-1',3'-dioxolan-4'-yl)-1,3-dioxolan-4-yl)methanol
42927-35-5

((2S,3R)-2,2-dimethyl-5-((4'R,5'S)-2',2',5'-trimethyl-1',3'-dioxolan-4'-yl)-1,3-dioxolan-4-yl)methanol

(2S,3R)-2,2-dimethyl-5-((4'R,5'S)-2',2',5'-trimethyl-1',3'-dioxolan-4'-yl)-1,3-dioxolane-4-carbaldehyde
212065-83-3

(2S,3R)-2,2-dimethyl-5-((4'R,5'S)-2',2',5'-trimethyl-1',3'-dioxolan-4'-yl)-1,3-dioxolane-4-carbaldehyde

Conditions
ConditionsYield
With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical In dichloromethane at 0 - 20℃;82%

87-90-1Relevant articles and documents

Preparation method of omeprazole midbody

-

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 trichloroisocyanuric acid

-

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.

A two-stage continuous chlorination method for production of trichloro isocyanuric acid

-

Paragraph 0027-0034, (2017/03/28)

The invention discloses a method for producing trichloro-isocyanuric acid by virtue of two-stage continuous chlorination. A production process of the method comprises first-stage chlorination reaction and second-stage chlorination reaction; an excessive amount of chlorine is fed into a second-stage reaction kettle, a cyanuric acid trisodium salt solution is continuously added into a first-stage reactor, the excessive amount of chlorine in the second-stage reaction kettle is sucked into the first-stage reactor for chlorination reaction by virtue of an ejection pump of a first-stage reaction system, and a reaction liquid overflows into the second-stage reaction kettle to continuously react to generate trichloro-isocyanuric acid. The chlorination reaction degree of materials inside the one-stage reactor and the chlorine feeding amount of the second-stage reaction kettle are controlled by virtue of the reaction temperature of the first-stage reactor. The method is small in amount of chlorination mother liquid and high in reaction efficiency, and a gas discharged from the first-stage reactor is free of chlorine. The time that the material is retained in the chlorination reaction system is short, so that side reaction can be reduced, the effective chlorine of a product is kept greater than 90%, and the yield is more than 86%.

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