13036-83-4

Basic information

• Product Name: 1,3,5-TRIBUTYLHEXAHYDRO-1,3,5-TRIAZINE
• Synonyms: 1,3,5-TRIBUTYLHEXAHYDRO-1,3,5-TRIAZINE;1,3,5-TRI-N-BUTYLHEXAHYDRO-S-TRIAZINE;1,3,5-Triazine, 1,3,5-tributylhexahydro-;1,3,5-TRIBUTYLHEXAHYDRO-1,3,5-TRIAZINE 98+%;1,3,5-Tributylhexahydro-s-triazine;1,3,5-Tributylhexahydro-1,3,5-trizine;1,3,5-tributyl-1,3,5-triazinane
• CAS NO: 13036-83-4
• Molecular Formula: C₁₅H₃₃N₃
• Molecular Weight: 255.44
• EINECS: 235-905-1
• Mol File: 13036-83-4.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 285℃
• Flash Point: 124.3±10.3℃
• Appearance: /
• Density: 0.876±0.06 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 0.000579mmHg at 25°C
• Refractive Index: 1.4575 (20℃)
• CAS DataBase Reference: 1,3,5-TRIBUTYLHEXAHYDRO-1,3,5-TRIAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-TRIBUTYLHEXAHYDRO-1,3,5-TRIAZINE(13036-83-4)
• EPA Substance Registry System: 1,3,5-TRIBUTYLHEXAHYDRO-1,3,5-TRIAZINE(13036-83-4)

Safety Data

• Hazardous Substances Data: 13036-83-4(Hazardous Substances Data)

Usage

General Description

1,3,5-Tributylhexahydro-1,3,5-triazine is a chemical compound represented by the molecular formula C12H27N3. As part of the alkyl 1,3,5-triazines, it falls under the classification of organic compounds known as dialkylarylamines. It typically appears as a liquid and may have industrial and commercial uses. Currently, limited literature specifically details this chemical, meaning its properties, chemical behavior or toxicological data are not described in detail. It is advised to handle such chemicals with care and appropriate precautions, considering potential safety risks particularly in absence of exhaustive information.

InChI:InChI=1/C15H33N3/c1-4-7-10-16-13-17(11-8-5-2)15-18(14-16)12-9-6-3/h4-15H2,1-3H3

Upstream product

• 50-00-0 formaldehyd 
• 109-73-9 N-butylamine 
• 5577-66-2 trimethyl(butyl-amino)silane 
• 44426-86-0 N-methylidenebutylamine 
• 75-09-2 dichloromethane 

Downstream Products

• 33704-65-3 Butyl-phenylsulfanylmethyl-amine; hydrochloride 
• 110-68-9 N-n-butyl-N-methylamine 
• 63235-64-3 1-butyl-5-methyl-4-phenylimidazole 3-oxide 
• 64-18-6 formic acid 
• 109-73-9 N-butylamine 
• 1426581-64-7 methyl 4-(4-bromophenylamino)-1-butyl-2,5-dihydro-5-oxo-1H-pyrrole-3-carboxylate 

Relevant articles and documents

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Synthesis and Crystal Structure of Dipotassium Salts of N-Alkyl-N-{[O-alkoxy(hydroxy)phosphoryl]methyl}ditiocarbamic Acids

Abstract: A one-pot method for the synthesis of dipotassium salts of N-alkyl-N-{[O-alkoxy(hydroxy)phosphoryl]methyl}dithiocarbamic acids has been elaborated. Dipotassium salts of N-isopropyl-, N-butyl-, and N-cyclohexyl-N-{[hydroxy(O-ethoxy)phosphoryl]methyl}dithiocarbamic acids as well as N-{[O-butoxy(hydroxy)phosphoryl]methyl}-N-(2-methoxyethyl)dithiocarbamic acid have been synthesized and isolated. Crystal and molecular structure of the latter compound have been elucidated.

REACTIONS OF DICHLOROMETHANE WITH THIOANIONS. 2. FORMATION OF 5-ALKYL-1,3,5-DITHIAZINANES, 3,5-DIALKYL-1,3,5-THIADIAZINANES, AND 1,3,5-TRIALKYL-1,3,5-TRIAZINANES BY REACTION OF DICHLOROMETHANE WITH SODIUM SULFIDE AND MONOALKYLAMINES

The reaction of dichloromethane with sodium sulfide and monoalkylamines, catalyzed by polyethyleneglycol 1,500, is studied.A mixture of 5-alkyl-1,3,5-dithiazinane, 3,5-dialkyl-1,3,5-thiadiazinane, and 1,3,5-trialkyl-1,3,5-triazinane is obtained.The proportion of these heterocycles depends on the amine structure and the presence of sodium hydroxide. - Key words: 5-Alkyl-1,3,5-dithiazinanes; 3,5-dialkyl-1,3,5-thiadiazinanes; dichloromethane double substitution; polyethyleneglycol as catalyst