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130001

Sigma-Aldrich

1-Methylpiperazine

99%

Synonyme(s) :

N-Methylpiperazine

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About This Item

Formule empirique (notation de Hill):
C5H12N2
Numéro CAS:
Poids moléculaire :
100.16
Numéro Beilstein :
102724
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22

Densité de vapeur

3.5 (vs air)

Niveau de qualité

Pureté

99%

Forme

liquid

Indice de réfraction

n20/D 1.466 (lit.)

Point d'ébullition

138 °C (lit.)

Densité

0.903 g/mL at 25 °C (lit.)

Chaîne SMILES 

CN1CCNCC1

InChI

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

Clé InChI

PVOAHINGSUIXLS-UHFFFAOYSA-N

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Catégories apparentées

Description générale

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

Application

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.

Pictogrammes

FlameCorrosionExclamation mark

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

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

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

88.7 °F - closed cup

Point d'éclair (°C)

31.5 °C - closed cup

Équipement de protection individuelle

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
S A Leach et al.
Carcinogenesis, 8(12), 1907-1912 (1987-12-01)
Human exposure to endogenously formed N-nitroso compounds has frequently been suggested as a causative factor in carcinogenesis where this is related to chronic bacterial infection such as is seen in gastric achlorhydria. At least two distinct mechanisms of endogenous formation
A R Roudman et al.
Journal of biomedical materials research, 39(4), 667-672 (1998-03-10)
Aminated poly(vinyl chloride) (PVC) membranes were prepared that had a Nernstian response over a wide range of pH. The reaction between PVC and methyl-piperazine (MePIP) in dimethylformamide (DMF) was studied over a wide range of time and temperature, and in

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