Names | |
---|---|
Preferred IUPAC name
1-Methylpiperazine | |
Other names
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.003.309 |
EC Number |
|
PubChem
CID
|
|
UNII | |
UN number | 2920 |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C5H12N2 | |
Molar mass | 100.165 g·mol−1 |
Melting point | −6 °C (21 °F; 267 K) [1] |
Boiling point | 138 °C (280 °F; 411 K) [1] |
Hazards | |
GHS labelling: | |
Danger | |
H226, H312, H314, H317, H330, H331, H332 | |
P210, P233, P240, P241, P242, P243, P260, P261, P264, P271, P272, P280, P284, P301+P330+P331, P302+P352, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P310, P311, P312, P320, P321, P322, P333+P313, P363, P370+P378, P403+P233, P403+P235, P405, P501 | |
NFPA 704 (fire diamond) | |
Safety data sheet (SDS) | FischerSci |
Related compounds | |
Related compounds
|
Piperazine, 4-methylpyridine |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
N-Methylpiperazine is a heterocyclic organic compound.
N-Methylpiperazine is a common building block used in organic synthesis. [2] For example, N-methylpiperazine is used in the manufacture of various pharmaceutical drugs including cyclizine, [3] meclizine, and sildenafil.
The lithium salt, lithium N-methylpiperazide, is used as a reagent in organic synthesis for protection of aryl aldehydes. [4]
Industrially, N-methylpiperazine is produced by reacting diethanolamine and methylamine at 250 bar and 200 °C. [5] [6]
{{
cite book}}
: CS1 maint: multiple names: authors list (
link)
Names | |
---|---|
Preferred IUPAC name
1-Methylpiperazine | |
Other names
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.003.309 |
EC Number |
|
PubChem
CID
|
|
UNII | |
UN number | 2920 |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C5H12N2 | |
Molar mass | 100.165 g·mol−1 |
Melting point | −6 °C (21 °F; 267 K) [1] |
Boiling point | 138 °C (280 °F; 411 K) [1] |
Hazards | |
GHS labelling: | |
Danger | |
H226, H312, H314, H317, H330, H331, H332 | |
P210, P233, P240, P241, P242, P243, P260, P261, P264, P271, P272, P280, P284, P301+P330+P331, P302+P352, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P310, P311, P312, P320, P321, P322, P333+P313, P363, P370+P378, P403+P233, P403+P235, P405, P501 | |
NFPA 704 (fire diamond) | |
Safety data sheet (SDS) | FischerSci |
Related compounds | |
Related compounds
|
Piperazine, 4-methylpyridine |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
N-Methylpiperazine is a heterocyclic organic compound.
N-Methylpiperazine is a common building block used in organic synthesis. [2] For example, N-methylpiperazine is used in the manufacture of various pharmaceutical drugs including cyclizine, [3] meclizine, and sildenafil.
The lithium salt, lithium N-methylpiperazide, is used as a reagent in organic synthesis for protection of aryl aldehydes. [4]
Industrially, N-methylpiperazine is produced by reacting diethanolamine and methylamine at 250 bar and 200 °C. [5] [6]
{{
cite book}}
: CS1 maint: multiple names: authors list (
link)