13036-81-2

Basic information

• Product Name: 1,3,5-TRI-N-PROPYL HEXAHYDRO-S-TRIAZINE
• Synonyms: 1,3,5-TRI-N-PROPYL HEXAHYDRO-S-TRIAZINE;hexahydro-1,3,5-tripropyl-1,3,5-triazine;1,3,5-Triazine, hexahydro-1,3,5-tripropyl-;Hexahydro-1,3,5-tripropyl-s-triazine;Ai3-51515;Einecs 235-904-6;1,3,5-Tripropyl-1,3,5-triazinane;1,3,5-Tri-n-propylhexahydro-1,3,5-triazine
• CAS NO: 13036-81-2
• Molecular Formula: C₁₂H₂₇N₃
• Molecular Weight: 213.36
• EINECS: 235-904-6
• Mol File: 13036-81-2.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 94℃/0.7mm
• Flash Point: 101.9°C
• Appearance: Colorless/Liquid
• Density: 0.880
• Vapor Pressure: 0.00975mmHg at 25°C
• Refractive Index: 1.4660
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 1,3,5-TRI-N-PROPYL HEXAHYDRO-S-TRIAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-TRI-N-PROPYL HEXAHYDRO-S-TRIAZINE(13036-81-2)
• EPA Substance Registry System: 1,3,5-TRI-N-PROPYL HEXAHYDRO-S-TRIAZINE(13036-81-2)

Safety Data

• TSCA: Yes
• Hazardous Substances Data: 13036-81-2(Hazardous Substances Data)

Usage

General Description

1,3,5-Tri-N-Propyl Hexahydro-S-Triazine is a chemical compound known for its versatile utility in various industries. This organic compound belongs to the class of organic compounds known as 1,3,5-triazinanes, which are six-membered heterocyclic rings made up of three nitrogen, atom, and three carbon atoms. Notably, it can function effectively as an additive in lubricants due to its friction-reducing characteristics. It also plays a significant role in the synthesis of polymeric materials. Despite its numerous applications, it is essential to handle it carefully because it might offer potential health risks when improperly dealt with.

InChI:InChI=1/C12H27N3/c1-4-7-13-10-14(8-5-2)12-15(11-13)9-6-3/h4-12H2,1-3H3

Upstream product

• 107-10-8 propylamine 
• 75-09-2 dichloromethane 
• 50-00-0 formaldehyd 

Downstream Products

• 6794-92-9 1,2-di-n-propyldiaziridine 
• 452056-84-7 N-{4-[5-(4-fluorophenyl)-1-oxy-3-propyl-3H-imidazol-4-yl]pyridin-2-yl}acetamide 
• 107-10-8 propylamine 
• 627-35-0 methyl-n-propylamine 

Relevant articles and documents

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Catalyst for curable compositions containing hexahydrotriazine structural units

A compound containing at least one hexahydrotriazine unit of formula (I) having at least one amidine or guanidine group and to the use thereof as a catalyst for the crosslinking of a functional compound, in particular a polymer including silane groups. The compound contains at least one hexahydrotriazine unit of formula (I) is producible in a simple process from readily available feedstocks, odorless at room temperature, non-volatile and largely non-toxic. The compound accelerates the crosslinking of functional polymers surprisingly well and by simple variation of the substituents is variable such that it has very good compatibility in different polymers as a result of which such compositions do not have a propensity for migration-based defects such as separation, exudation or substrate contamination.

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