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Key Documents

139505

Sigma-Aldrich

2-(2-Aminoethyl)-1-methylpyrrolidine

97%

Synonyme(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

Formule empirique (notation de Hill):
C7H16N2
Numéro CAS:
Poids moléculaire :
128.22
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22

Pureté

97%

Forme

liquid

Indice de réfraction

n20/D 1.4684 (lit.)

Densité

0.885 g/mL at 25 °C (lit.)

Chaîne SMILES 

CN1CCCC1CCN

InChI

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

Clé InChI

PNHGJPJOMCXSKN-UHFFFAOYSA-N

Description générale

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.

Pictogrammes

CorrosionExclamation mark

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

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

Organes cibles

Respiratory system

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

149.0 °F - closed cup

Point d'éclair (°C)

65 °C - closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Consulter la Bibliothèque de documents

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.
Molecular biology of the cell, 26(1), 43-54 (2014-11-08)
Lymphocyte function-associated antigen 1 (LFA-1, CD11a/CD18, αLβ2-integrin) and its ligands are essential for adhesion between T-cells and antigen-presenting cells, formation of the immunological synapse, and other immune cell interactions. LFA-1 function is regulated through conformational changes that include the modulation

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