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1,2-dimethylpyrrolidine

  • Product Name1,2-dimethylpyrrolidine
  • cas765-48-0
  • purity99%
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Factory Sells Best Quality 1,2-dimethylpyrrolidine 765-48-0 with GMP standards

  • Molecular Formula:C6H13N
  • Molecular Weight:99.1759
  • Vapor Pressure:47.6mmHg at 25°C 
  • Refractive Index:1.4268 (estimate) 
  • Boiling Point:94.3°C at 760 mmHg 
  • PKA:10.2(at 26℃) 
  • PSA:3.24000 
  • Density:0.828g/cm3 
  • LogP:1.03840 

1,2-dimethylpyrrolidine(Cas 765-48-0) Usage

Physical state

Colorless to yellow liquid

Odor

Fishy

Solvent properties

Often used as a solvent

Organic synthesis

Used in organic synthesis

Pharmaceutical applications

Used in the manufacture of pharmaceuticals

Agrochemical applications

Used in the manufacture of agrochemicals

Polymerization

Used as an initiator in radical and cationic polymerization

Antioxidants

Utilized as an intermediate in the production of antioxidants

Rubber accelerators

Utilized as an intermediate in the production of rubber accelerators

Corrosion inhibitors

Utilized as an intermediate in the production of corrosion inhibitors

Feed additive

Studied for potential use as a feed additive

Co-solvent

Studied for use as an effective co-solvent in lithium-ion batteries

Solvating properties

Has solvating properties

Stabilizing properties

Has stabilizing properties

Diverse applications

Used in various industries due to its diverse properties

General Description

1,2-Dimethylpyrrolidine is a chemical compound with the molecular formula C7H13N. It is a colorless to yellow liquid with a fishy odor, often used as a solvent and in organic synthesis. 1,2-dimethylpyrrolidine is primarily used in the manufacture of pharmaceuticals, agrochemicals, and as a initiator in radical and cationic polymerization. It is also utilized as an intermediate in the production of antioxidants, rubber accelerators, and corrosion inhibitors. Additionally, 1,2-dimethylpyrrolidine has been studied for its potential use as a feed additive and as an effective co-solvent in lithium-ion batteries. Overall, this chemical compound has diverse applications in various industries due to its solvating and stabilizing properties.

InChI:InChI=1/C6H13N/c1-6-4-3-5-7(6)2/h6H,3-5H2,1-2H3

765-48-0 Relevant articles

AMMONIUM SALT, ELECTROLYTE FOR LITHIUM SECONDARY BATTERY, AND LITHIUM SECONDARY BATTERY USING THEM

-

Paragraph 0051; 0065, (2017/12/01)

PROBLEM TO BE SOLVED: To provide: ammoni...

IONIC LIQUID

-

Paragraph 0194; 0195, (2016/10/08)

PROBLEM TO BE SOLVED: To provide an ioni...

Hydroamination/cyclization of aminoalkenes using cationic zirconocene and titanocene catalysts

Gribkov, Denis V.,Hultzsch, Kai C.

, p. 5542 - 5546 (2007/10/03)

Alternative catalysts: The hydroaminatio...

Organolanthanide-catalyzed hydroamination. A kinetic, mechanistic, and diastereoselectivity study of the cyclization of N-unprotected amino olefins

Gagné, Michel R.,Stern, Charlotte L.,Marks, Tobin J.

, p. 275 - 294 (2007/10/02)

This contribution reports the efficient,...

765-48-0 Process route

3,4-dihydro-1,5-dimethyl-2H-pyrrolium perchlorate
2730-96-3

3,4-dihydro-1,5-dimethyl-2H-pyrrolium perchlorate

toluene
108-88-3,15644-74-3,16713-13-6

toluene

acetonitrile
75-05-8,26809-02-9

acetonitrile

1,2-dimethylpyrrolidine
765-48-0,802254-03-1,802822-49-7

1,2-dimethylpyrrolidine

1,1'-(1,2-ethanediyl)bisbenzene
103-29-7

1,1'-(1,2-ethanediyl)bisbenzene

dihydrocinnamonitrile
645-59-0

dihydrocinnamonitrile

Conditions
Conditions Yield
for 4h; Product distribution; Quantum yield; Irradiation; effect of arene;
7%
4%
1,1,2-trimethyl-pyrrolidinium; chloride

1,1,2-trimethyl-pyrrolidinium; chloride

1,2-dimethylpyrrolidine
765-48-0,802254-03-1,802822-49-7

1,2-dimethylpyrrolidine

methylene chloride
74-87-3

methylene chloride

Conditions
Conditions Yield

765-48-0 Upstream products

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765-48-0 Downstream products

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    123489-62-3

    4,4'-bis<(2-methylpyrrolidino)acetyl>biphenyl dimethiobromide

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