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130001

Sigma-Aldrich

1-Methylpiperazin

99%

Synonym(e):

N-Methylpiperazine

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About This Item

Empirische Formel (Hill-System):
C5H12N2
CAS-Nummer:
109-01-3
Molekulargewicht:
100.16
Beilstein:
102724
EG-Nummer:
203-639-5
MDL-Nummer:
MFCD00005966
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24847936
NACRES:
NA.22

Dampfdichte

3.5 (vs air)

Qualitätsniveau

200

Assay

99%

Form

liquid

Brechungsindex

n20/D 1.466 (lit.)

bp

138 °C (lit.)

Dichte

0.903 g/mL at 25 °C (lit.)

SMILES String

CN1CCNCC1

InChI

1S/C5H12N2/c1-7-4-2-6-3-5-7/h6H,2-5H2,1H3

InChIKey

PVOAHINGSUIXLS-UHFFFAOYSA-N

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Allgemeine Beschreibung

1-Methylpiperazine is a heterocyclic diamine used as a versatile building block and intermediate in organic synthesis.

Anwendung

1-Methylpiperazine was used as mimic template in the preparation of molecularly imprinted microspheres (MIMs). It was also used to prepare the difunctional strong anion-exchange stationary phase from a 1,4-diazacyclohexane derivative.

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - Skin Sens. 1B

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 1

Flammpunkt (°F)

88.7 °F - closed cup

Flammpunkt (°C)

31.5 °C - closed cup

Persönliche Schutzausrüstung

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

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Juxiang Ruan et al.
Journal of chromatography. A, 1297, 77-84 (2013-06-01)
This paper reports the preparation of a novel, silica-based, strong anion-exchange stationary phase from a 1,4-diazacyclohexane derivative. To prepare the difunctional strong anion-exchange stationary phase, activated silica beads were first bonded with 3-chloropropyltriethoxysilane and then reacted with 1-methylpiperazine followed by
Hongyuan Yan et al.
The Analyst, 137(12), 2884-2890 (2012-05-04)
A highly selective molecularly imprinted solid-phase extraction (MISPE) combined with liquid chromatography-ultraviolet detection was developed for the simultaneous isolation and determination of four plant hormones including indole-3-acetic acid (IAA), indole-3-propionic acid (IPA), indole-3-butyric acid (IBA) and 1-naphthaleneacetic acid (NAA) in
E Gavathiotis et al.
Nucleic acids research, 28(3), 728-735 (2000-01-19)
The solution structure of the dodecamer duplex d(CTTTTGCAAAAG)(2)and its 2:1 complex with the bis -benzimidazole Hoechst 33258 has been investigated by NMR and NOE-restrained molecular dynamics (rMD) simulations. Drug molecules are bound in each of the two A-tracts with the
Andrius Žilionis
European journal of mass spectrometry (Chichester, England), 26(1), 25-35 (2019-08-21)
Liquid chromatography-tandem mass spectrometry is one of the most sensitive tools for determination of trace amounts of analytes in metabolomics and proteomics. The highest sensitivity is achieved in selected reaction monitoring detection, which involves fragmentation of the molecular ion between
Olesya A Troshina et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 12(21), 5569-5577 (2006-06-07)
An oxidative radical photoaddition of mono N-substituted piperazines to [60]fullerene was systematically investigated. Reactions of C60 with piperazines bearing bulky electron-withdrawing groups (2-pyridyl, 2-pyrimidinyl) were found to be the most selective and yielded C60(amine)4O as major products along with small
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