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139505

Sigma-Aldrich

2-(2-Aminoethyl)-1-methylpyrrolidine

97%

Sinonimo/i:

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

Formula empirica (notazione di Hill):
C7H16N2
Numero CAS:
51387-90-7
Peso molecolare:
128.22
Numero CE:
257-169-0
Numero MDL:
MFCD00003175
Codice UNSPSC:
12352100
ID PubChem:
24848416
NACRES:
NA.22

Livello qualitativo

100

Saggio

97%

Stato

liquid

Indice di rifrazione

n20/D 1.4684 (lit.)

Densità

0.885 g/mL at 25 °C (lit.)

Gruppo funzionale

amine

Stringa SMILE

CN1CCCC1CCN

InChI

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

Categorie correlate

Descrizione generale

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.

Applicazioni

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.

Pittogrammi

CorrosionExclamation mark
GHS05,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H302,H315,H318,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

149.0 °F - closed cup

Punto d’infiammabilità (°C)

65 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
MKBD6022
08209AH
08421JE
02602PC
19715BI

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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
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
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
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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