571261

Piperidine

biotech. grade, ≥99.5%

• Synonym(s): Hexahydropyridine
• Empirical Formula (Hill Notation): C₅H₁₁N
• CAS Number: 110-89-4
• Molecular Weight: 85.15
• UNSPSC Code: 12352005
• NACRES: NA.21
• PubChem Substance ID: 329758271
• EC Number: 203-813-0
• Beilstein/REAXYS Number: 102438
• MDL number: MFCD00005979
• Assay: ≥99.5%
• Grade: biotech. grade
• Technique(s): DNA sequencing: suitable
• Bp: 106 °C
• Vapor pressure: 23 mmHg ( 20 °C)

Properties

• grade: biotech. grade
• Quality Segment: 100
• vapor density: 3 (vs air)
• vapor pressure: 23 mmHg ( 20 °C)
• assay: ≥99.5%
• form: liquid
• technique(s): DNA sequencing: suitable
• impurities: <0.3% water
• refractive index: n20/D 1.452 (lit.)
• bp: 106 °C
• mp: −13 °C (lit.)
• solubility: organic solvents: soluble(lit.), water: miscible(lit.)
• density: 0.862 g/mL at 20 °C (lit.)
• λ: 1 cm path, H₂O reference
• UV absorption: λ: 290 A_max: <1.000, λ: 370 A_max: <0.050
• SMILES string: C1CCNCC1
• InChI: 1S/C5H11N/c1-2-4-6-5-3-1/h6H,1-5H2
• InChI key: NQRYJNQNLNOLGT-UHFFFAOYSA-N

Description

General description

Piperidine, a heterocyclic cyclohexane is a volatile secondary amine. Maxam-Gilbert chemical method, a DNA sequencing technology employs piperidine to rupture DNA strands at damaged base site. Its crystal structure analyzed at 150K shows hydrogen bonding between NH groups. Piperidine ring forms a part of many naturally occuring alkaloids. It is prepared on an industrial scale by the hydrogenation of pyridine in the presence of nickel catalyst. The ¹H NMR spectrum of piperidine has been recorded.

Our biotech solvents offer exceptional quality for reliable RNA extraction, ensuring optimal laboratory performance. With low water content and minimal residue, give clean UV spectra to minimize contamination.

• High-Quality Biotech Solvents: Designed for optimal laboratory performance with low water content and minimal residues.
• Ideal for RNA Extraction: Essential for genetic testing and research applications like PCR.
• Ensures Integrity of Genetic Material: Promotes reliable and reproducible results.
• Industry Compliant: Suitable for both academic and commercial laboratories, enhancing research efficiency.

Application

Piperidine has been used in combination with DMF (dimethylformamide) for the removal of Fmoc (fluorenylmethyloxycarbonyl) group from the N-terminal amino group during peptide synthesis.

Fits Applied Biosystems 431 and 433A peptide synthesizers.

Safety Information

• pictograms: GHS02,GHS06,GHS05
• signalword: Danger
• hcodes: H225,H302,H311 + H331,H314
• pcodes: P210 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
• Hazard Classifications: Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
• Storage Class: 3 - Flammable liquids
• wgk: WGK 1
• flash_point_f: 60.8 °F - closed cup
• flash_point_c: 16 °C - closed cup