HEXAHYDRO-1,3,5-TRIETHYL-S-TRIAZINE

PRODUCT IDENTIFICATION

CAS NO. 7779-27-3

HEXAHYDRO-1,3,5-TRIETHYL-S-TRIAZINE

EINECS NO. 231-924-4
FORMULA C9H21N3
MOL WT. 171.29

H.S. CODE

 

TOXICITY

 
SYNONYMS Triethylhexahydro-s-triazine; Hexahydro-1,3,5-triethyl-s-triazine;
1,3,5-Triethylhexahydro-s-triazine; Triethyltrimethylenetriamine; Hexahidro-1,3,5-trietil-1,3,5-triazina; Hexahydro-1,3,5-triéthyl-1,3,5-triazine;
RAW MATERIALS

 

CLASSIFICATION

 

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE white powder
MELTING POINT  
BOILING POINT 207 - 208 C
SPECIFIC GRAVITY 0.89 - 0.90
SOLUBILITY IN WATER  
pH  
VAPOR DENSITY

5.91

REFRACTIVE INDEX

1.4585 - 1.4605

NFPA RATINGS

Health: 2; Flammability: 0; Instability: 0

AUTOIGNITION

 

FLASH POINT

 

STABILITY Stable under ordinary conditions

APPLICATIONS

Triazine is the chemical species of six-membered heterocyclic ring compound with three nitrogens replacing carbon-hydrogen units in the benzene ring structure. The names of the three isomers indicate which of the carbon-hydrogen units on the benzene ring position of the molecule have been replaced by nitrogens, called 1,2,3-triazine, 1,2,4-triazine, and 1,3,5-triazine respectively. Symmetrical 1,3,5-triazine is the common. Triazines are prepared from 2-azidocyclopropene through thermal rearrangement (1,2,3-triazine), from 1,2-dicarbonyl compound with amidrazone by condensation reaction (1,2,4-triazine) and from cyanic acid amide by trimerization (1,3,5-triazine). Pyridine is the aromatic nitrogen heterocycle compound having only one nitrogen, and diazines are with 2 nitrogen atoms and tetrazines are with 4 nitrogen atoms on the benzene ring system. Triazines are weak base. Triazines have much weaker resonance energy than  benzene, so nucleophilic substitution is preferred than electrophilic substitution. Triazines are basic structure of herbicides, examples are amitole (CAS #: 61-82-5), atrazine (CAS #: 1912-24-9), cyanazine (CAS #: 21725-46-2), simazine (CAS #: 122-34-9), trietazine (CAS #: 1912-26-1). Large volume of triazines are used in  the manufacture of resin modifiers such as melamine and benzoguanamine.  Melamine (1,3,5-Triazine-2,4,6-triamine) is reacted with formaldehyde to from a very durable thermoset resin. Benzoguanamine (2,4-Diamino-6-phenyl-1,3,5-triazine) is used to increase thermoset properties of alkyd, acrylic and formaldehyde resins. Triazines are also useful as chromophore groups in colorants and Chlorine attached in Triazine compounds undergo nucleophilic substitution reactions well with with hydroxyl groups in cellulose fibres. Some triazine family compounds are used in pharmaceutical industry as coupling agent for the synthesis of peptide in solid phase as well as solution and as side chain of antibiotics. Triazine compounds are used in formulating bactericide and fungicide. They are used as  preservatives in oil field applications. They are used as disinfectant, industrial deodorant and biocide in water treatment. They are used as a bleaching agents.

Hexahydro-1,3,5-triethyl-s-triazine is used in formulating bactericide and fungicide. It is used as a preservative in oil field applications.

SALES SPECIFICATION

APPEARANCE

clear to yellowish liquid

PURITY

98.0% min

TRANSPORTATION
PACKING
180kgs in drum
HAZARD CLASS  
UN NO.  
OTHER INFORMATION
Hazard Symbols: XI, Risk Phrases: 36/37/38, Safety Phrases: 24/25