42729-56-6

Basic information

• Product Name: 1-ISOPROPYL-3-PYRROLIDINOL
• Synonyms: 1-ISOPROPYL-3-HYDROXYPYRROLIDINE;1-ISOPROPYL-3-PYRROLIDINOL;1-ISOPROPYL-3-PYRROLIDINOL 95+%;1-isopropylpyrrolidin-3-ol
• CAS NO: 42729-56-6
• Molecular Formula: C₇H₁₅NO
• Molecular Weight: 129.2
• Mol File: 42729-56-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 118 °C / 33mmHg
• Flash Point: 60.2 °C
• Appearance: /
• Density: 0,96 g/cm3
• Vapor Pressure: 0.132mmHg at 25°C
• Refractive Index: 1.4670 to 1.4720
• PKA: 14.83±0.20(Predicted)
• CAS DataBase Reference: 1-ISOPROPYL-3-PYRROLIDINOL(CAS DataBase Reference)
• NIST Chemistry Reference: 1-ISOPROPYL-3-PYRROLIDINOL(42729-56-6)
• EPA Substance Registry System: 1-ISOPROPYL-3-PYRROLIDINOL(42729-56-6)

Safety Data

• Safety Statements: 23-24/25
• Hazardous Substances Data: 42729-56-6(Hazardous Substances Data)

Usage

General Description

1-Isopropyl-3-Pyrrolidinol, also known as IPP, is a chemical compound that belongs to the class of pyrrolidinols. It is commonly used as a solvent and surfactant in various industrial applications, including in the production of personal care products, detergents, and cleaning agents. IPP is also utilized as a stabilizer and emulsifier in the formulation of cosmetics and pharmaceuticals. Additionally, it has antimicrobial properties and is often incorporated into disinfectant and sanitizing products. IPP is known for its low toxicity and high biodegradability, making it a preferred choice for use in consumer products and industrial processes.

InChI:InChI=1/C7H15NO/c1-6(2)8-4-3-7(9)5-8/h6-7,9H,3-5H2,1-2H3

Upstream product

• 2419-74-1 1,4-dichlorobutan-2-ol 
• 75-31-0 isopropylamine 
• 40499-83-0 pyrrolidin-3-ol 
• 67-64-1 acetone 
• 19398-47-1 1,4-dibromo-2-butanol 

Downstream Products

• 1430842-15-1 2-((2,4-dichlorobenzyl)oxy)benzaldehyde O-(1-isopropylpyrrolidin-3-yl) oxime 
• 1430842-14-0 2-((3-fluorobenzyl)oxy)benzaldehyde O-(1-isopropylpyrrolidin-3-yl) oxime 
• 1430842-13-9 2-((3,4-dichlorobenzyl)oxy)benzaldehyde O-(1-isopropylpyrrolidin-3-yl) oxime 
• 1430842-12-8 2-(benzyloxy)benzaldehyde O-(1-isopropylpyrrolidin-3-yl) oxime 
• 1430842-11-7 3-(trifluoromethyl)benzaldehyde O-(1-isopropylpyrrolidin-3-yl) oxime 
• 1430842-10-6 2-methoxybenzaldehyde O-(1-isopropylpyrrolidin-3-yl) oxime 
• 912947-12-7 4-(1-Isopropyl-pyrrolidin-3-yloxy)-benzonitrile 
• 1061749-46-9 C₂₄H₃₀N₆O₂ 

Relevant articles and documents

Preparation method of N-substituent-3-hydroxytetrahydropyrrole

The invention discloses a preparation method of N-substituent-3-hydroxytetrahydropyrrole. The preparation method takes 1,2,4-butanetriol as a starting material, and comprises the following steps: performing a halogenating reaction between the starting material and hydrogen halide to prepare an intermediate 1,4-dihalogeno-2-butanol first, and then performing a condensation reaction with primary amine RNH2 to obtain a target product, wherein R represents methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tertiary butyl or benzyl; the halogenating reaction is performed in the presence of an acidic catalyst, and the acidic catalyst is formic acid or acetic acid; and hydrogen halide is hydrogen chloride or hydrogen bromide. The preparation method disclosed by the invention is relatively short in synthetic route, the starting material 1,2,4-butanetriol is low in price and easy to obtain, and other materials used in the method are relatively high in safety and also relatively low in price, so that the preparation method is suitable for industrial large-scale production. Particularly, the halogenating reaction can obtain a yield of 50% or above by selection of suitable halogenating agents and catalysts.