哌啶

Name: 哌啶
Brand: SIGALD

biotech. grade, ≥99.5%

别名:

六氢吡啶

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About This Item

经验公式（希尔记法）:

C₅H₁₁N

CAS Number:

110-89-4

分子量:

85.15

Beilstein:

102438

EC 号:

203-813-0

MDL编号:

MFCD00005979

UNSPSC代码:

12352005

PubChem化学物质编号:

329758271

NACRES:

NA.21

主要文件

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等级

biotech. grade

质量水平

100

蒸汽密度

3 (vs air)

蒸汽压

23 mmHg ( 20 °C)

方案

≥99.5%

表单

liquid

技术

DNA sequencing: suitable

杂质

<0.3% water

折射率

n20/D 1.452 (lit.)

沸点

106 °C (lit.)
106 °C

mp

−13 °C (lit.)

溶解性

organic solvents: soluble(lit.)
water: miscible(lit.)

密度

0.862 g/mL at 20 °C (lit.)

λ

1 cm path, H₂O reference

紫外吸收

λ: 290 A_max: <1.000
λ: 370 A_max: <0.050

SMILES字符串

C1CCNCC1

InChI

1S/C5H11N/c1-2-4-6-5-3-1/h6H,1-5H2

InChI key

NQRYJNQNLNOLGT-UHFFFAOYSA-N

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一般描述

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.

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.

应用

适用于 Applied Biosystems 431 和 433A 多肽合成仪。

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.