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PX1235

Supelco

Piperidine

Synonym(s):

Piperidine, Hexahydropyridine

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100 MG
CN¥2,176.58

CN¥2,176.58


Estimated to ship onMay 08, 2025Details


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100 MG
CN¥2,176.58

About This Item

Empirical Formula (Hill Notation):
C5H11N
CAS Number:
Molecular Weight:
85.15
MDL number:
UNSPSC Code:
12191504
EC Index Number:
203-813-0

Assay:
≥99.5% (GC)
bp:
106 °C/1013 hPa
vapor pressure:
34 hPa ( 20 °C)

CN¥2,176.58


Estimated to ship onMay 08, 2025Details


Request a Bulk Order

vapor pressure

34 hPa ( 20 °C)

Quality Level

Assay

≥99.5% (GC)

form

liquid

impurities

≤0.2% Water (H2O)

color

APHA: ≤50

pH

12.6 (20 °C, 100 g/L in H2O)

bp

106 °C/1013 hPa

mp

-10.8 °C

transition temp

flash point 16 °C

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This Item
SAB5801046SAB5801047SAB5801005
clone

recombinant monoclonal

clone

recombinant monoclonal

clone

recombinant monoclonal

clone

polyclonal

biological source

alpaca

biological source

alpaca

biological source

alpaca

biological source

alpaca

conjugate

horse radish peroxidase (HRP)

conjugate

unconjugated (6*his tag and one cys were added at the C terminal of the VHH)

conjugate

biotin

conjugate

horse radish peroxidase (HRP)

species reactivity

human, Alpaca

species reactivity

Alpaca, human

species reactivity

Alpaca, human

species reactivity

Alpaca, mouse

mol wt

14 kDa

mol wt

14 kDa

mol wt

14 kDa

mol wt

14 kDa

Application

Piperidine can be used as:
  • A Fmoc removal agent in solid-phase peptide synthesis.[1]
  • An organic structure-directing agent in the synthesis of ferrierite zeolites and CoAPO (cobalt aluminophosphate) materials.[2][3]
  • A reagent in the preparation of N-(2,4-dinitrophenyl)piperidine by reacting with 2,4-dinitrochlorobenzene via aromatic nucleophilic substitution reaction.[4]

Analysis Note

Assay (GC): 99.5% min
Color (APHA): 50APHA max
Form: Clear liquid
Identity (IR-spectrum): Conforms
Water (H2O): 0.2% max

Signal Word

Danger

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 Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

60.8 °F - closed cup

Flash Point(C)

16 °C - closed cup

Regulatory Information

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    Solvent effects on aromatic nucleophilic substitutions. Part 3. The kinetics of the reaction of 2, 4-dinitrochlorobenzene with piperidine in aprotic solvents
    Mancini PME, et al.
    J. Chem. Soc. Perkin Trans. II, (7), 1133-1138 (1984)
    Thermal investigations of CoAPO materials prepared by using piperidine as a structure-directing agent
    Rajic N, et al.
    Thermochimica Acta, 351(1-2), 119-124 (2000)
    Synthesis of FER zeolite with piperidine as structure-directing agent and its catalytic application
    Chu Weifeng, et al.
    Chinese Journal of Catalysis, 38(11), 1880-1887 (2017)
    Omar F Luna et al.
    Molecules (Basel, Switzerland), 21(11) (2016-11-18)
    The deprotection step is crucial in order to secure a good quality product in Fmoc solid phase peptide synthesis. 9-Fluorenylmethoxycarbonyl (Fmoc) removal is achieved by a two-step mechanism reaction favored by the use of cyclic secondary amines; however, the efficiency

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