4-Methylpiperidine | Pharmaceutical Grade | 99.99% Purity | 10mg 20mg 30mg Vials | Lyophilized Powder |626-58-4

4-Methylpiperidine Basic information
Product Name: 4-Methylpiperidine
Synonyms: LABOTEST-BB LTBB000596;HEXAHYDRO-G-PICOLINE;GAMMA-PIPECOLINE;4-METHYLPIPERIDINE;4-PIPECOLINE;4PPC;4-methyl-piperidin;4-pipecoline(gamma-)
CAS: 626-58-4
MF: C6H13N
MW: 99.17
EINECS: 210-954-1
Product Categories: Chemical Synthesis;Heterocyclic Building Blocks;Piperidine;Building Blocks;C5 to C7;Piperidines;K00001;YP00036
Mol File: 626-58-4.mol
Shop 4-Methylpiperidine626-58-4-Detailed Image 1

4-Methylpiperidine Chemical Properties
Melting point 4-5 °C
Boiling point 124 °C(lit.)
density 0.838 g/mL at 25 °C(lit.)
vapor pressure 16 hPa (20 °C)
refractive index n20/D 1.446(lit.)
Fp 45 °F
storage temp. Flammables area
solubility Chloroform
pka pK1:11.23(+1) (25°C,μ=0.5)
form Liquid
color Clear slightly yellow
Specific Gravity 0.838
PH 13 (100g/l, H2O, 20℃)
Water Solubility miscible
BRN 1083
InChI 1S/C6H13N/c1-6-2-4-7-5-3-6/h6-7H,2-5H2,1H3
InChIKey UZOFELREXGAFOI-UHFFFAOYSA-N
SMILES CC1CCNCC1
CAS DataBase Reference 626-58-4(CAS DataBase Reference)
NIST Chemistry Reference Piperidine, 4-methyl-(626-58-4)
EPA Substance Registry System Piperidine, 4-methyl- (626-58-4)

Safety Information
Hazard Codes F,Xi,T
Risk Statements 11-36/37/38-36-20/21-10-61
Safety Statements 16-26-36-45-36/37-53
RIDADR UN 1993 3/PG 2
WGK Germany 3
TSCA TSCA listed
HazardClass 3
PackingGroup II
HS Code 29333999
Storage Class 3 - Flammable liquids
Hazard Classifications Acute Tox. 4 Oral
Eye Dam. 1
Flam. Liq. 2
Skin Corr. 1B
MSDS Information
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4-Methylpiperidine Usage And Synthesis
Chemical Properties clear slightly yellow liquid
Uses 4-Methylpiperidine is used as a catalyst in the synthesis of stilbene derivatives as anti-malarial agents. It also serves as an anti-corrosive compound for iron.
Uses 4-Methylpiperidine acts as a catalyst in the preparation of stilbene derivatives. It is used as an anti-corrosive compound for iron. It is also used in the synthesis of peptides to remove or deprotection of 9-fluorenylmethyloxycarbonyl (Fmoc) groups.
Purification Methods Purify it via the hydrochloride (m 189o). It is freed from 3-methylpyridine by zone melting. The hydrobromide has m 173o(from butanone/*C6H6). [Beilstein 20 III/IV 1511, 20/4 V 116.]

4-Methylpiperidine Preparation Products And Raw materials
Preparation Products 2-(4-METHYL-PIPERIDIN-1-YL)-ETHYLAMINE-->4-METHYLENEPIPERIDINE-->4-Methyl-1,2,3,6-tetrahydropyridine-->1-(CHLOROACETYL)-4-METHYLPIPERIDINE-->1-Piperidineacetic acid, 4-methyl-, ethyl ester-->4-METHYLNITROSOPIPERIDINE-->2-chloro-6-(4-methylpiperidine-1-carbonyl)pyridine-->2,2-DIMETHYL-3-(4-METHYL-PIPERIDIN-1-YL)-PROPIONALDEHYDE-->(4-AMINO-PHENYL)-(4-METHYL-PIPERIDIN-1-YL)-METHANONE-->(4-(CHLOROMETHYL)PIPERIDIN-1-YL)(PHENYL)METHANONE-->4-(4-methylpiperidin-1-yl)benzaldehyde-->(2R,4R)-1-[(2S)-2-[(tert-Butyloxycarbonyl)aMino]-5-[[iMino(nitroaMino)Methyl]aMino]-1-oxopentyl]-4-Methyl-2-piperidinecarboxylic Acid Benzyl Ester