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139505

Sigma-Aldrich

2-(2-Aminoethyl)-1-methylpyrrolidine

97%

Synonym(s):

1-Methyl-2-(2-aminoethyl)pyrrolidine, 1-Methyl-2-pyrrolidineethanamine, 2-(1-Methyl-2-pyrrolidinyl)ethanamine, 2-(1-Methyl-2-pyrrolidinyl)ethylamine, 2-(1-Methylpyrrolidin-2-yl)ethan-1-amine, 2-(1-Methylpyrrolidin-2-yl)ethylamine, 2-(2-Aminoethyl)-1-methylpyrrolidine, 2-(N-Methylpyrrolidin-2-yl)ethylamine, N-Methyl-2-(2-aminoethyl)pyrrolidine

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About This Item

Empirical Formula (Hill Notation):
C7H16N2
CAS Number:
51387-90-7
Molecular Weight:
128.22
EC Number:
257-169-0
MDL number:
MFCD00003175
UNSPSC Code:
12352100
PubChem Substance ID:
24848416
NACRES:
NA.22

Quality Level

100

Assay

97%

form

liquid

refractive index

n20/D 1.4684 (lit.)

density

0.885 g/mL at 25 °C (lit.)

SMILES string

CN1CCCC1CCN

InChI

1S/C7H16N2/c1-9-6-2-3-7(9)4-5-8/h7H,2-6,8H2,1H3

InChI key

PNHGJPJOMCXSKN-UHFFFAOYSA-N

Related Categories

General description

2-(2-Aminoethyl)-1-methylpyrrolidine labelling acts as probe within microfluidic chip for electrochemiluminescence detection. It acts as electrogenerated chemiluminescence derivatization reagent for carboxylic acid in HPLC.

Application

2-(2-Aminoethyl)-1-methylpyrrolidine was used in dual-cloud point extraction and tertiary amine labeling for the quantification of indole-3-acetic acid and indole-3-butyric acid.

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H315,H318,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 2

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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M C Stoll et al.
The American journal of emergency medicine, 32(10), 1300-1300 (2014-05-23)
Thoracic injury following a major trauma can be life threatening. Veno-venous extracorporeal membrane oxygenation (vv-ECMO) can be used as a support to mechanical ventilation when acute respiratory distress syndrome is present. We report the case of an 18-year-old male driver
Xue-Bo Yin et al.
Journal of chromatography. A, 1217(8), 1399-1406 (2009-12-29)
The low concentrations of the auxins in samples of plant tissue necessitate the use of selective and sensitive techniques for their quantification. Herein a selective and sensitive method based on dual-cloud point extraction (dCPE) and tertiary amine labeling for the
D F Ranney
Journal of supramolecular structure, 5(3), 335-342 (1976-01-01)
Microtubule-disrupting alkaloids and protein fixatives were used to investigate the nature of an active process that must occur within stimulator cells in order for them to initiate a unidirectional mixed lymphocyte response (MLR). Brief treatment of the stimulator cells (SC)
Hirotoshi Morita et al.
Analytical chemistry, 74(7), 1584-1589 (2002-05-30)
2-(2-Aminoethyl)-1-methylpyrrolidine and N-(3-aminopropyl)pyrrolidine (NAPP) were found to be selective and sensitive derivatization reagents for carboxylic acid by high-performance liquid chromatography (HPLC) with electrogenerated chemiluminescence detection using tris(2,2'-bipyridine)ruthenium(II). Free fatty acids and ibuprofen were used as model compounds of carboxylic acids
Alexandre Chigaev et al.
BMC immunology, 9, 26-26 (2008-06-07)
Activation of integrins in response to inside-out signaling serves as a basis for leukocyte arrest on endothelium, and migration of immune cells. Integrin-dependent adhesion is controlled by the conformational state of the molecule (i.e. change in the affinity for the
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