1-Methylpiperidin-4-amine supplier

Name
1-Methylpiperidin-4-amine
EINECS
CAS No. 41838-46-4
Article Data27
CAS DataBase
Density 0.913 g/cm³
Solubility
Melting Point 203-207 °C
Formula C₆H₁₄N₂
Boiling Point 141.015 °C at 760 mmHg
Molecular Weight 114.191
Flash Point 39.197 °C
Transport Information
Appearance colorless to light-yellow liquid
Safety 26-36/37/39
Risk Codes 36/37/38
Molecular Structure
Hazard Symbols Xi
Synonyms Piperidine,4-amino-1-methyl- (6CI,7CI);1-Methyl-4-aminopiperidine;1-Methyl-4-piperidinamine;4-Amino-1-methylpiperidine;N-Methyl-4-aminopiperidine;4-Piperidinamine,1-methyl-;
PSA 29.26000
LogP 0.67750

Synthetic route

: 1445-73-4
1-Methyl-4-piperidone

: 41838-46-4
1-methyl-4-aminopiperidine

Conditions

Conditions	Yield
With ammonium formate; palladium on carbon In methanol	100%
With ammonium formate; palladium on activated charcoal In methanol; water at 20℃;	75%
With ammonium formate; palladium on activated charcoal In methanol; water at 20℃;	37%

: 34737-83-2
1-methylpiperidin-4-one hydrochloride

: 41838-46-4
1-methyl-4-aminopiperidine

Conditions

Conditions	Yield
Stage #1: 1-methylpiperidin-4-one hydrochloride With ammonium acetate In methanol for 0.166667h; Stage #2: With sodium cyanoborohydride In methanol for 1h;	88%
With ammonium acetate; sodium cyanoborohydride In methanol for 1.16667h;	88%

: C6H12N2

: 41838-46-4
1-methyl-4-aminopiperidine

Conditions

Conditions	Yield
With sodium tetrahydroborate at 5℃; for 12h; Reflux; Large scale;	85.3%

: 359878-09-4
N-((4-methylphenyl)methyl)-N-(1-piperidin-4-yl)-4-chlorophenylacetamide

: 41838-46-4
1-methyl-4-aminopiperidine

Conditions

Conditions	Yield
With formic acid; palladium 10% on activated carbon In methanol for 24h; Heating / reflux;	51%

: 359878-55-0
4-(4-methoxybenzylamino)-1-methylpiperidine

: 41838-46-4
1-methyl-4-aminopiperidine

Conditions

Conditions	Yield
With formic acid; palladium 10% on activated carbon In methanol for 24h; Inert atmosphere; Reflux;	51%

: 84540-61-4
1-methyl-piperidin-4-one oxime ; hydrochloride

: 41838-46-4
1-methyl-4-aminopiperidine

Conditions

Conditions	Yield
With ethanol; sodium Heating;	50%

: 1515-27-1
1-methyl-4-piperidinone oxime

: 64-17-5
ethanol

: 41838-46-4
1-methyl-4-aminopiperidine

Conditions

Conditions	Yield
With sodium

: 1515-27-1
1-methyl-4-piperidinone oxime

: 41838-46-4
1-methyl-4-aminopiperidine

Conditions

Conditions	Yield
With i-Amyl alcohol; sodium

: 145344-76-9
N-(1-methyl-[4]piperidyl)-acetamide

: 41838-46-4
1-methyl-4-aminopiperidine

Conditions

Conditions	Yield
With hydrogenchloride

: 62718-28-9
1-methylpiperidine-4-carboxamide

: 41838-46-4
1-methyl-4-aminopiperidine

Conditions

Conditions	Yield
With potassium hydroxide; bromine

: 13221-89-1, 56026-45-0
1-methyl-4-oxo-piperidine-3-carboxylic acid methyl ester

: 41838-46-4
1-methyl-4-aminopiperidine

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: water; hydrochloric acid 3: isopentyl alcohol; sodium View Scheme

: 1445-73-4
1-Methyl-4-piperidone

NH4 OAc: NH4 OAc

: 41838-46-4
1-methyl-4-aminopiperidine

Conditions

Conditions	Yield
With hydrogenchloride; NaCNBH3; silica gel In methanol; diethyl ether	3.88 g (88%)
With hydrogenchloride; NaCNBH3; silica gel In methanol; diethyl ether	3.88 g (88%)

: 118306-22-2
4-chlorocarbonyl-4,9-dihydro-1-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one

A: 41838-46-4
1-methyl-4-aminopiperidine

B: 4,9-dihydro-1-methyl-4-{[(1-methyl-4-piperidinyl)amino]carbonyl}-10H-thieno[3,4-b][1,5]benzodiazepin-10-one

: 118306-21-1
4-(chlorocarbonyl)-4,9-dihydro-3-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one

A: 41838-46-4
1-methyl-4-aminopiperidine

B: 4,9-Dihydro-3-methyl-4-{[(1-methyl-4-piperidinyl)amino]carbonyl}-10H-thieno[3,4-b][1,5]benzodiazepin-10-one

: 118306-23-3
4-(chlorocarbonyl)-4,9-dihydro-1,3-dimethyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one

A: 41838-46-4
1-methyl-4-aminopiperidine

B: 4,9-dihydro-1,3-dimethyl-4-{[(1-methyl-4-piperidinyl)amino]carbonyl}-10H-thieno[3,4-b][1,5]benzodiazepin-10-one

: 65220-86-2
1-(trifluoroacetyl)-4-piperidone

: 41838-46-4
1-methyl-4-aminopiperidine

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1.1: sodium cyanoborohydride; acetic acid / methanol / 20 h / pH ~ 5 1.2: pH ~ 10 2.1: triethylamine / dichloromethane / 0.17 h / 0 °C 2.2: 1.25 h / 0 °C 3.1: potassium carbonate / methanol / 24 h / 40 °C 4.1: formic acid / palladium 10% on activated carbon / methanol / 24 h / Heating / reflux View Scheme

: 359878-15-2
4-(4-methylbenzylamino)-1-(trifluoroacetyl)piperidine

: 41838-46-4
1-methyl-4-aminopiperidine

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1.1: triethylamine / dichloromethane / 0.17 h / 0 °C 1.2: 1.25 h / 0 °C 2.1: potassium carbonate / methanol / 24 h / 40 °C 3.1: formic acid / palladium 10% on activated carbon / methanol / 24 h / Heating / reflux View Scheme

: 359879-83-7
2-(4-chlorophenyl)-N-(4-methylbenzyl)-N-(1-trifluoroacetylpiperidin-4-yl)acetamide

: 41838-46-4
1-methyl-4-aminopiperidine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: potassium carbonate / methanol / 24 h / 40 °C 2: formic acid / palladium 10% on activated carbon / methanol / 24 h / Heating / reflux View Scheme

: 359877-52-4
tert-butyl 4-((4-methylphenyl)methyl)aminopiperidine carboxylate

: 41838-46-4
1-methyl-4-aminopiperidine

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 h / 20 °C 1.2: 2 h 2.1: hydrogenchloride / 1,4-dioxane; diethyl ether / 2 h / 20 °C 3.1: formic acid / palladium 10% on activated carbon / methanol / 24 h / Heating / reflux View Scheme

: C26H33ClN2O3

: 41838-46-4
1-methyl-4-aminopiperidine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: hydrogenchloride / 1,4-dioxane; diethyl ether / 2 h / 20 °C 2: formic acid / palladium 10% on activated carbon / methanol / 24 h / Heating / reflux View Scheme

: 41979-39-9
4-piperidone hydrochloride

: 41838-46-4
1-methyl-4-aminopiperidine

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 1.1: triethylamine / dichloromethane / 0.17 h / 0 °C 1.2: 2 h / 20 °C 2.1: sodium cyanoborohydride; acetic acid / methanol / 20 h / pH ~ 5 2.2: pH ~ 10 3.1: triethylamine / dichloromethane / 0.17 h / 0 °C 3.2: 1.25 h / 0 °C 4.1: potassium carbonate / methanol / 24 h / 40 °C 5.1: formic acid / palladium 10% on activated carbon / methanol / 24 h / Heating / reflux View Scheme

Yield

Multi-step reaction with 5 steps
1.1: triethylamine / dichloromethane / 0.17 h / 0 °C
1.2: 2 h / 20 °C
2.1: sodium cyanoborohydride; acetic acid / methanol / 20 h / pH ~ 5
2.2: pH ~ 10
3.1: triethylamine / dichloromethane / 0.17 h / 0 °C
3.2: 1.25 h / 0 °C
4.1: potassium carbonate / methanol / 24 h / 40 °C
5.1: formic acid / palladium 10% on activated carbon / methanol / 24 h / Heating / reflux
View Scheme

: 79099-07-3
N-tert-butyloxycarbonylpiperidin-4-one

: 41838-46-4
1-methyl-4-aminopiperidine

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1.1: sodium cyanoborohydride; acetic acid / methanol / 20 h / 20 °C 1.2: 1 h 2.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 h / 20 °C 2.2: 2 h 3.1: hydrogenchloride / 1,4-dioxane; diethyl ether / 2 h / 20 °C 4.1: formic acid / palladium 10% on activated carbon / methanol / 24 h / Heating / reflux View Scheme

: 41838-46-4
1-methyl-4-aminopiperidine

: 1001345-80-7
2‐fluoro‐5‐methoxy‐4‐nitrobenzoic acid

: 1001345-79-4
2-fluoro-5-methoxy-N-(1-methylpiperidin-4-yl)-4-nitrobenzamide

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine; HATU In ISOPROPYLAMIDE at 18 - 25℃; for 1h;	100%
With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl acetamide at 18 - 25℃; for 1h;	100%

: 41838-46-4
1-methyl-4-aminopiperidine

: 455-87-8
4-amino-3-fluorobenzoic acid

: 1001345-97-6
4-amino-3-fluoro-N-(1-methylpiperidin-4-yl)benzamide

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 18 - 25℃; for 18h;	100%
With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl acetamide at 18 - 25℃; for 18h;	100%

: 41838-46-4
1-methyl-4-aminopiperidine

: 112704-79-7
2-fluoro-4-bromobenzoic acid

: 893420-55-8
4-bromo-2-fluoro-N-(1-methylpiperidin-4-yl)benzamide

Conditions

Conditions	Yield
Stage #1: 4-Amino-1-methylpiperidine; 2-fluoro-4-bromobenzoic acid With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 1.5h; Stage #2: With sodium hydroxide In water at 20℃;	100%
With triethylamine; HATU In N,N-dimethyl-formamide

: 41838-46-4
1-methyl-4-aminopiperidine

: 60771-18-8
7-(benzyloxy)-2,4-dichloro-6-methoxyquinazoline

: 1197196-50-1
7-(benzyloxy)-2-chloro-6-methoxy-N-(1-methylpiperidin-4-yl)quinazolin-4-amine

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃;	100%
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃;	100%
at 20℃;

: 41838-46-4
1-methyl-4-aminopiperidine

: 1367870-32-3
5-amino-4-methyl-1-phenyl-1H-pyrazole-3-carboxylic acid

: 1610455-25-8
5-amino-4-methyl-N-(1-methylpiperidin-4-yl)-1-phenyl-1H-pyrazole-3-carboxamide

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 20℃; for 5.5h;	100%

: 41838-46-4
1-methyl-4-aminopiperidine

: 4-(7-bromo-2,6-dichloro-8-fluoroquinazolin-4-yl)piperazine-1-carboxylic acid tert-butyl ester

: tert-butyl 4-(7-bromo-6-chloro-8-fluoro-2-((1-methylpiperidin-yl)amino)quinazolin-4-yl)piperazine-1-carboxylate

Conditions

Conditions	Yield
With potassium fluoride In dimethyl sulfoxide at 120℃; for 1h;	100%

: 41838-46-4
1-methyl-4-aminopiperidine

: 1137477-51-0
N-(5-bromo-4-chloropyridin-2-yl)pivalamide

: 1137477-53-2
N-(5-bromo-4-(1-methylpiperidin-4-ylamino)pyridin-2-yl)pivalamide

Conditions

Conditions	Yield
In 1-methyl-pyrrolidin-2-one at 220℃; for 3h; Microwave irradiation;	99%

: 41838-46-4
1-methyl-4-aminopiperidine

: 630125-49-4
1-bromo-3-nitro-5-(trifluoromethyl)benzene

: 1529769-59-2
1-methyl-N-[3-nitro-5-(trifluoromethyl)phenyl]piperidin-4-amine

Conditions

Conditions	Yield
With palladium diacetate; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In 1,4-dioxane at 120℃; Inert atmosphere;	99%
With palladium diacetate; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In 1,4-dioxane at 120℃; Inert atmosphere;	99%

: 41838-46-4
1-methyl-4-aminopiperidine

: 364-73-8
4-Bromo-1-fluoro-2-nitrobenzene

: N-(4-bromo-2-nitrophenyl)-1-methylpiperidin-4-amine

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran at 0 - 20℃; Inert atmosphere;	99%
With caesium carbonate In N,N-dimethyl-formamide at 20℃; for 8h;

: 41838-46-4
1-methyl-4-aminopiperidine

: 364793-54-4
6-bromo-4-chloro-3-quinolinecarbonitrile

: 6-bromo-4-[(1-methylpiperidin-4-yl)amino]quinoline-3-carbonitrile

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In isopropyl alcohol at 100℃; for 0.5h; Microwave irradiation;	99%

: 41838-46-4
1-methyl-4-aminopiperidine

: 2-(4-isocyanatophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

: 879486-87-0
N-(1-methyl-piperidin-4-yl)-N'-[4-(4,4,5,5-tetramethyl-1,3,2-dioxoborolan-2-yl)-phenyl]-urea

Conditions

Conditions	Yield
In dichloromethane at 20℃; for 5h;	98%
In 1,2-dimethoxyethane

: 41838-46-4
1-methyl-4-aminopiperidine

: 3113-71-1
3-methyl-4-nitrobenzoic acid

: 1001345-96-5
3-methyl-N-(1-methyl-4-piperidyI)-4-nitro-benzamide

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 18 - 25℃; for 18h;	98%

: 41838-46-4
1-methyl-4-aminopiperidine

: 1829-33-0
3-chloro-5-hydroxybenzaldehyde

: 3-chloro-5-{[(1-methylpiperidin-4-yl)amino]methyl}phenol

Conditions

Conditions	Yield
With sodium tris(acetoxy)borohydride In dichloromethane at 20℃; for 18.5h;	97%

: 41838-46-4
1-methyl-4-aminopiperidine

: 1493-27-2
ortho-nitrofluorobenzene

: 600725-12-0
N-(1-methyl-piperidin-4-yl)-benzene-1,2-diamine

Conditions

Conditions	Yield
	96%

: 41838-46-4
1-methyl-4-aminopiperidine

: 1024599-54-9
5-(1,1-difluoroethyl)-2-methyl-2H-pyrazole-3-carboxylic acid

: C13H20F2N4O

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In 1-methyl-pyrrolidin-2-one at 90℃; for 0.166667h; Microwave irradiation;	96%

: 41838-46-4
1-methyl-4-aminopiperidine

: 3-(cyclopentyloxy)-4-nitrobenzoic acid

: 3-(cyclopentyloxy)-N-(1-methylpiperidin-4-yl)-4-nitrobenzamide

Conditions

Conditions	Yield
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine In N,N-dimethyl-formamide at 20℃; for 16h; Inert atmosphere;	96%

: 41838-46-4
1-methyl-4-aminopiperidine

: 16024-82-1
methyl 2-isothiocyanatobenzoate

: 3-(1-methyl-4-piperidyl)-2-thioxo-1H-quinazolin-4-one

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran at 150℃; for 0.75h; Microwave irradiation;	96%

: 41838-46-4
1-methyl-4-aminopiperidine

: 400-74-8
2-Fluoro-5-nitrobenzotrifluoride

: 1183289-25-9
(1-methyl-piperidin-4-yl)-(4-nitro-2-trifluoromethyl-phenyl)-amine

Conditions

Conditions	Yield
In tetrahydrofuran at 20℃; for 4h;	95%

: 41838-46-4
1-methyl-4-aminopiperidine

: 103058-87-3
5-bromo-2-methoxypyridine-3-carboxaldehyde

: N-((5-bromo-2-methoxypyridin-3-yl)methyl)-1-methylpiperidin-4-amine

Conditions

Conditions	Yield
With sodium cyanoborohydride; acetic acid In methanol at 20℃; for 22h;	94%

: 41838-46-4
1-methyl-4-aminopiperidine

: 403-21-4
3-fluoro-4-nitrobenzoic acid

: 3-fluoro-N-(1-methylpiperidin-4-yl)-4-nitrobenzamide

Conditions

Conditions	Yield
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine In N,N-dimethyl-formamide at 20℃; for 16h; Inert atmosphere;	94%

: 41838-46-4
1-methyl-4-aminopiperidine

: 4521-61-3
3,4,5-Trimethoxybenzoyl chloride

: 3,4,5-Trimethoxy-N-(1-methyl-piperidin-4-yl)-benzamide

Conditions

Conditions	Yield
In benzene Ambient temperature;	93%

: 41838-46-4
1-methyl-4-aminopiperidine

: 4-bromo-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole-3-carboxylic acid

: 4-bromo-N-(1-methylpiperidin-4-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole-3-carboxamide

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 0 - 20℃; for 4h; Inert atmosphere;	92.4%

: 41838-46-4
1-methyl-4-aminopiperidine

: 874-60-2
4-methyl-benzoyl chloride

: N-(1-methyl-[4]piperidyl)-p-toluamide

Conditions

Conditions	Yield
In benzene Ambient temperature;	92%

: 41838-46-4
1-methyl-4-aminopiperidine

: 27631-29-4
2-chloro-6,7-dimethoxy-3H-quinazolin-4-one

: 1197196-66-9
2-chloro-6,7-dimethoxy-N-(1-methylpiperidin-4-yl)quinazolin-4-amine

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 2h;	92%
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 2h;	92%
With potassium carbonate In N,N-dimethyl-formamide at 20℃;	90%

: 41838-46-4
1-methyl-4-aminopiperidine

: 62-23-7
4-nitro-benzoic acid

: 210643-97-3
N-(1-methylpiperidin-4-yl)-4-nitrobenzamide

Conditions

Conditions	Yield
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine In N,N-dimethyl-formamide at 20℃; for 16h; Inert atmosphere;	92%
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0 - 20℃;	17.39%
With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 35℃; for 4h;

: 41838-46-4
1-methyl-4-aminopiperidine

: 3‐{[8‐(1‐methyl‐1H‐indol‐6‐yl)quinoxalin‐6‐yl]amino}pyridine‐4‐carboxylic acid

: 3‐{[8‐(1‐methyl‐1H‐indol‐6‐yl)quinoxalin‐6‐yl]amino}‐N‐(1‐methylpiperidin‐4‐yl)pyridine‐4‐carboxamide

Conditions

Conditions	Yield
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In 1,4-dioxane at 20℃; for 24h;	92%
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In 1,4-dioxane at 20℃; for 24h; Inert atmosphere;	92%

: 41838-46-4
1-methyl-4-aminopiperidine

: 16588-16-2
ethyl 4-chloro-3-nitrobenzoate

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 70℃; for 16h;	92%

1-methyl-4-aminopiperidine: 1-methyl-4-aminopiperidine

: 2719-27-9
cyclohexanylcarbonyl chloride

: Cyclohexanecarboxylic acid (1-methyl-piperidin-4-yl)-amide

Conditions

Conditions	Yield
In benzene Ambient temperature;	91%

: 41838-46-4
1-methyl-4-aminopiperidine

: 10263-19-1
3',4',5'-trimethoxycinnamoyl chloride

: (E)-N-(1-Methyl-piperidin-4-yl)-3-(3,4,5-trimethoxy-phenyl)-acrylamide

Conditions

Conditions	Yield
In benzene Ambient temperature;	91%

1-Methylpiperidin-4-amine Chemical Properties

IUPAC Name: 1-Methylpiperidin-4-amine
Molecular Formula: C₆H₁₄N₂
Molecular Weight: 114.19 g/mol
Canonical SMILES: CN1CCC(CC1)N
InChI: InChI=1S/C6H14N2/c1-8-4-2-6(7)3-5-8/h6H,2-5,7H2,1H3
Product Categories: Pyridine; API intermediates
XLogP3-AA: -0.1
H-Bond Donor: 1
H-Bond Acceptor: 2
Index of Refraction: 1.469
Molar Refractivity: 34.88 cm³
Molar Volume: 125 cm³
Polarizability: 13.82×10^-24 cm³
Surface Tension: 30.8 dyne/cm
Density: 0.912 g/cm³
Flash Point: 39.2 °C
Enthalpy of Vaporization: 37.82 kJ/mol
Boiling Point: 141 °C at 760 mmHg
Melting Point: 203-207 °C
Vapour Pressure of 1-Methylpiperidin-4-amine (CAS NO.41838-46-4): 5.97 mmHg at 25 °C

1-Methylpiperidin-4-amine Safety Profile

Hazard Codes: Irritant Xi
Risk Statements: 36/37/38
R36/37/38: Irritating to eyes, respiratory system and skin.
Safety Statements: 26-36/37/39
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39: Wear suitable protective clothing, gloves and eye/face protection.
Hazard Note: Irritant
HazardClass of 1-Methylpiperidin-4-amine (CAS NO.41838-46-4): Irritant

1-Methylpiperidin-4-amine Specification

1-Methylpiperidin-4-amine (CAS NO.41838-46-4), its Synonyms are 4-Amino-1-methylpiperidine ; 1-Methyl-4-Amino Piperidine ; N-Methyl-4-aminopiperidine ; 1-(5-Bromopyrimidin-2-yl)[1,4]diazepane ; 4-Amino-1-methyl-piperidine ; 4-Amino-1-methylpiperidine 97% ; 4-Piperidinamine, 1-methyl- .

Product Name

1-Methylpiperidin-4-amine

Synthetic route

1-Methylpiperidin-4-amine Chemical Properties

1-Methylpiperidin-4-amine Safety Profile

1-Methylpiperidin-4-amine Specification

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