52198-64-8

Basic information

• Product Name: N1-tert-butylpropane-1,3-diaMine
• Synonyms: N1-tert-butylpropane-1,3-diaMine;N1-(1,1-dimethylethyl)-1,3-Propanediamine
• CAS NO: 52198-64-8
• Molecular Formula: C₇H₁₈N₂
• Molecular Weight: 130.23122
• Mol File: 52198-64-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 172.2°C at 760 mmHg
• Flash Point: 63.2°C
• Appearance: /
• Vapor Pressure: 1.35mmHg at 25°C
• CAS DataBase Reference: N1-tert-butylpropane-1,3-diaMine(CAS DataBase Reference)
• NIST Chemistry Reference: N1-tert-butylpropane-1,3-diaMine(52198-64-8)
• EPA Substance Registry System: N1-tert-butylpropane-1,3-diaMine(52198-64-8)

Safety Data

• Hazardous Substances Data: 52198-64-8(Hazardous Substances Data)

Usage

Description

N1-tert-butylpropane-1,3-diamine is an organic chemical compound with the molecular formula C7H18N2. It is a derivative of propane-1,3-diamine, also known as 1,3-diaminopropane, and the tert-butyl group is attached to the nitrogen atom. This colorless, viscous liquid with a strong ammonia-like odor is highly soluble in water and is commonly used as a curing agent in epoxy resins and as an intermediate in the synthesis of pharmaceuticals and other organic compounds.

Uses

Used in Epoxy Resin Industry:
N1-tert-butylpropane-1,3-diamine is used as a curing agent for epoxy resins, which are thermosetting polymers used in various applications such as coatings, adhesives, and composite materials. Its ability to react with epoxy groups and form cross-linked structures contributes to the final properties of the cured resin.
Used in Pharmaceutical Industry:
N1-tert-butylpropane-1,3-diamine is used as an intermediate in the synthesis of pharmaceuticals. Its chemical structure allows it to be a versatile building block for the development of various drug molecules, contributing to the creation of new therapeutic agents.
Used in Polyurethane Industry:
N1-tert-butylpropane-1,3-diamine is a vital component in the production of various polyurethane products, such as foams, adhesives, and coatings. Its role in the formation of polyurethane polymers helps to determine the physical and chemical properties of the final products, making it an essential ingredient in this industry.
It is important to handle N1-tert-butylpropane-1,3-diamine with care due to its potential irritant and corrosive effects on the skin, eyes, and respiratory system. Proper safety measures should be taken during its use and handling to minimize any adverse effects.

InChI:InChI=1/C7H18N2/c1-7(2,3)9-6-4-5-8/h9H,4-6,8H2,1-3H3/p+2

Upstream product

• 503-29-7 azetidine 
• 75-64-9 tert-butylamine 
• 21539-53-7 N-tert-butyl-β-alanine nitrile 

Downstream Products

• 15974-03-5 1-Benzylidenamino-3-tert-butylamino-propan 
• 103094-27-5 5-(3-tert-Butylamino-propylamino)-4-(2-fluoro-phenyl)-1,3-dimethyl-1,7-dihydro-pyrazolo[3,4-b]pyridin-6-one 
• 85723-42-8 2-(3-tert-Butylamino-propylamino)-N-[4-(2-fluoro-benzoyl)-2,5-dimethyl-2H-pyrazol-3-yl]-acetamide 
• 1422514-28-0 N₁-(tert-butyl)-N₃-(7-chloro-3-(4-(trifluoromethoxy)-phenyl)-quinolin-4-yl)propane-1,3-diamine 

Relevant articles and documents

NUCLEOPHILIC CLEAVAGE AND FORMATION OF SATURATED HETEROCYCLES. XII. REACTIVITY OF SMALL HETEROCYCLES TOWARD AMINOLYSIS AND HYDROLYSIS

The cleavage of four-membered saturated heterocycles proceeds via a more product-like transition state than that of three-membered rings.General acid catalysis is characteristic of oxygen heterocycles, but in the case of nitrogen heterocycles catalysis is specific.The reactivity of amines in the cleavage of azetidines is linearly dependent on their pKa values, primary and secondary amines comprising separate reaction series.