SDSDownload

1-Ethylpyrrolidine / 5 ML

Purity: 96.5'=103.5% (NT)\n97%\n
Synonym: N-Ethylpyrrolidine; 1-ethyl-pyrrolidine; N-ethyl-Tetrahydropyrrole
Molecular Formula: C6H13N
Molecular Weight: 99.17
SKU: MND-45184
CAS Number: 7335-06-0
MDL number: MFCD01632186
EC Number: 230-840-5
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 5 ML  
63.77 EUR



Safety Information


Hazard Statements

H225
H314

Precautionary Statements

P210
P280
P303 + P361 + P353
P264
P501
P305 + P351 + P338
P233
P240
P241
P242
P405
P403 + P235
P260
P243
P370 + P378
P363
P304 + P340
P301 + P330 + P331
P321
P316

Pictograms



Properties

Signal WordDanger
Flash Point (C)-22 °C
Flash Point (F)-7.6 °F

 Product Description

1-Ethylpyrrolidine is a heterocyclic organic compound consisting of a pyrrolidine ring with an ethyl group attached to the nitrogen atom. It is a colorless liquid used in chemical research and synthesis.

 

Application

1-Ethylpyrrolidine is utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves as a building block in various organic reactions, aiding in the development of complex molecules.

 

 

Articles:

- How do prolonged anchorage-free lifetimes strengthen non-small-cell lung cancer cells to evade anoikis? – A link with altered cellular metabolomics

Publication Date: 05 August 2023

Rungroch Sungthong, Hnin Ei Ei Khine, Somruethai Sumkhemthong, Pithi Chanvorachote, Rossarin Tansawat & Chatchai Chaotham

https://doi.org/10.1186/s40659-023-00456-z

 

- Iodine-catalyzed sulfonylation of sulfonyl hydrazides with tert-amines: a green and efficient protocol for the synthesis of sulfonamides

Publication Date: 2nd October 2019

Jinyang Chen, Xiaoran Han, Lan Mei, Jinchuan Liu, Kui Du, Tuanwu Cao and Qiang Li

https://doi.org/10.1039/C9RA07361B

 

- DEVELOPMENT OF AN EFFICIENT HPLC METHOD WITH PRE-COLUMN DERIVATIZATION FOR DETERMINATION OF ENANTIOMERIC PURITY OF 2-(AMINOMETHYL)-1-ETHYLPYRROLIDINE

Publication Date: mar. 2015

DAO-CAI WANG, TIAN YAO, GUO-FEI QIAN, LING-XIANG PU, SHUN YAO, HANG SONG

http://dx.doi.org/10.4067/S0717-97072015000100002