10105-42-7

Basic information

• Product Name: 1,3,5-triazine-2,4,6(1H,3H,5H)-trione trihydrazone
• Synonyms: 1,3,5-triazine-2,4,6(1H,3H,5H)-trione trihydrazone;cyanuric trihydrazide;1,3,5-Triazine-2,4,6(1H,3H,5H)-trione trishydrazone;2,4,6-Trihydrazino-1,3,5-triazine;1,3,5-Triazine, 2,4,6-trihydrazinyl-;Trihydrazine Triazine;2,4,6-trihydrazinyl-1,3,5-Triazine
• CAS NO: 10105-42-7
• Molecular Formula: C₃H₉N₉
• Molecular Weight: 171.16386
• EINECS: 233-288-3
• Mol File: 10105-42-7.mol
• Article Data: 7

Chemical Properties

• Melting Point: >300 °C (decomp)
• Boiling Point: 382.7 °C at 760 mmHg
• Flash Point: 185.2 °C
• Appearance: /
• Density: 2.41 g/cm³
• Vapor Pressure: 4.64E-06mmHg at 25°C
• Refractive Index: 2.107
• PKA: 1.74±0.20(Predicted)
• CAS DataBase Reference: 1,3,5-triazine-2,4,6(1H,3H,5H)-trione trihydrazone(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-triazine-2,4,6(1H,3H,5H)-trione trihydrazone(10105-42-7)
• EPA Substance Registry System: 1,3,5-triazine-2,4,6(1H,3H,5H)-trione trihydrazone(10105-42-7)

Safety Data

• Hazardous Substances Data: 10105-42-7(Hazardous Substances Data)

Usage

General Description

1,3,5-triazine-2,4,6(1H,3H,5H)-trione trihydrazone is a chemical compound with the molecular formula C3H9N6O3. It is a trihydrazide derivative of cyanuric acid and belongs to the class of triazine derivatives. The compound is used in various applications, including as a precursor for the synthesis of organic compounds and as a reagent in chemical research. It has also been studied for its potential use in medicinal and pharmaceutical applications due to its interesting properties and potential biological activities. 1,3,5-triazine-2,4,6(1H,3H,5H)-trione trihydrazone is an important chemical intermediate with a wide range of potential uses in various industrial and scientific fields.

InChI:InChI=1/C3H9N9/c4-10-1-7-2(11-5)9-3(8-1)12-6/h4-6H2,(H3,7,8,9,10,11,12)

Upstream product

• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 14921-00-7 cyanuric bromide 

Downstream Products

• 56519-16-5 3,3,7,7,11,11-hexaphenyl-2,3,6,7,10,11-hexahydro-tris[1,2,4,3]triazasilolo[4,5-a;4',5'-c;4'',5''-e][1,3,5]triazine 
• 1099616-49-5 C₁₅₃H₁₃₈N₁₂O₁₈ 

Relevant articles and documents

Synthesis, structure and third-order nonlinear optical properties of 1,3,5-triazine-based Zn(II) three-dimensional supramolecule

A novel zinc(II) 1,3,5-triazine-based complex [Zn(TIPT)Cl 2]·2CH3OH (1) (TIPT=2,4,6-tri(2-ispropylidene-1-ly) hydrazono-1,3,5-triazine) was prepared and structurally characterized by means of X-ray single crystal diffraction. The zinc(II) atom is coordinated at a distorted triangle bispyramid by three nitrogen atoms from TIPT and two Cl - anions. This compound exhibits a three-dimensional solid-state structure constituted by N-H?O, O-H?Cl, N-H?Cl and C-H?Cl hydrogen bonds. The third-order nonlinear optical properties were determined by Z-scan techniques. The results indicate the compound exhibit strong self-focusing effect, and the hyperpolarizability γ value is 8.26×10-30esu. Its thermal properties were also determined in air.

Hydrazino-methoxy-1,3,5-triazine derivatives' excellent corrosion organic inhibitors of steel in acidic chloride solution

The corrosion inhibition performance of 2-hydrazino-4,6-dimethoxy-1,3,5-tirazine (DMeHT), 2,4-dihydrazino-6-methoxy-1,3,5-triaizine (DHMeT), and 2,4,6-tridydrazino-1,3,5-triaizne (TH3 ) on steel corrosion in acidic media was examined using electrochemical techniques. The results showed 2,4-Ddihydrazino-6-methoxy-1,3,5-triaizine (DHMeT) gave the best corrosion protection performance among the other hydrazino derivatives even at a low concentration of 25 ppm (95%). The number of hydrazino groups play an important role in the corrosion inhibition, where the two hydrazine groups increased the electrostatic interactions between the protonated tested compounds, the negatively charged steel surface resulted from the adsorption of the chloride anions, and the presence of the methoxy group made the compound more reliable for formation of film protection on the surface of steel through the lone pair of oxygen atoms. Electrochemical Impedance Spectroscopy (EIS) measurements suggested that the corrosion process of steel in presence of the hydrazino-s-triazine derivatives (TH3 , DMeHT and DHMeT) were being controlled by the charge transfer reaction. Polarization curves indicated that the examined TH3 , DMeHT and DHMeT behaved as mixed type inhibitors.

Novel Anti-oxidant Compounds and Compositions

Trisubstituted triazine antioxidants.