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

1,3,5-trihydroxy-1,3,5-triazinane-2,4,6-trione - Names and Identifiers

Name	N N' N -TRIHYDROXYISOCYANURIC ACID
Synonyms	LT0053 N N' N -TRIHYDROXYISOCYANURIC ACID 1,3,5-trihydroxy-1,3,5-triazinane-2,4,6-trione 1,3,5-Trihydroxyhexahydro-1,3,5-triazine-2,4,6-trione 1,3,5-trihydroxy-1,3,5-Triazine-2,4,6(1H,3H,5H)-trione 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3,5-trihydroxy- 1N,3N,5N-trihydroxy-1,3,5-triazin-2,4,6[1H,3H,5H]-trione 2,?4,?6(1H,?3H,?5H)?-?trione, 1,?3,?5-?trihydroxy-?1,?3,?5-?Triazine
CAS	143435-52-3

1,3,5-trihydroxy-1,3,5-triazinane-2,4,6-trione - Physico-chemical Properties

Molecular Formula	C3H3N3O6
Molar Mass	177.07
Density	2.946±0.06 g/cm3(Predicted)
Melting Point	240-244°C (dec.)(lit.)
Boling Point	466.4±28.0 °C(Predicted)
pKa	8.29±0.20(Predicted)
Storage Condition	2-8℃
Physical and Chemical Properties	WGK Germany:1

1,3,5-trihydroxy-1,3,5-triazinane-2,4,6-trione - Risk and Safety

Hazard Symbols	T - Toxic
Risk Codes	61 - May cause harm to the unborn child
Safety Description	S53 - Avoid exposure - obtain special instructions before use. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
WGK Germany	1

1,3,5-trihydroxy-1,3,5-triazinane-2,4,6-trione - Introduction

N N' N-trihydroxyisocyyanuric ACID is an organic compound, often abbreviated as THP. The following is an introduction to the nature, use, preparation and safety information of THP:

Nature:
-THP is a colorless to pale yellow crystal with a special natural dewy smell.
-It is unstable to light and air, and can slowly decompose at room temperature.
-THP is soluble in many organic solvents, such as ethanol, acetone and dichloromethane.

Use:
-THP is an important organic synthesis intermediate, widely used in the synthesis of drugs, pesticides and other organic compounds.
-It can be used as an acetal agent, a protective group to prevent intramolecular alcohol dehydration reaction, and a chiral inducer for Chiral Induction of chiral compounds.

Method: There are many ways to prepare
-THP. The commonly used method is to react with aldehydes or ketones by Agar ketones under alkaline conditions.
-The reaction is usually carried out at room temperature, and the reactant is easily hydrolyzed under acidic conditions, so it needs to be carried out under basic conditions.
-The reaction can control the yield and selectivity of the product by adjusting the molar ratio of the reactants and the reaction conditions.

Safety Information:
-THP has not been listed as a harmful compound, but it still needs to follow regular laboratory safety procedures.
-During handling and storage, care should be taken to prevent contact with skin and eyes, and avoid inhaling dust or gas.
-When used in the laboratory, ensure good ventilation and wear suitable personal protective equipment, such as laboratory gloves and protective glasses.

Last Update：2024-04-09 20:49:11