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Merck

104094

Piperidine

99%, ReagentPlus®

Synonym(s):

Hexahydropyridine

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About This Item

Empirical Formula (Hill Notation):
C5H11N
CAS Number:
110-89-4
Molecular Weight:
85.15
NACRES:
NA.21
PubChem Substance ID:
24846636
UNSPSC Code:
12352100
EC Number:
203-813-0
MDL number:
MFCD00005979
Beilstein/REAXYS Number:
102438

Key Documents

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Product Name

Piperidine, ReagentPlus®, 99%

InChI key

NQRYJNQNLNOLGT-UHFFFAOYSA-N

InChI

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

SMILES string

C1CCNCC1

vapor density

2.94 (vs air)
3 (vs air)

vapor pressure

23 mmHg ( 20 °C)
23 mmHg ( 20 °C)

product line

ReagentPlus®

assay

99%

impurities

≤0.5% water (Karl Fischer)

refractive index

n20/D 1.452 (lit.)

bp

106 °C (lit.)

mp

−13 °C (lit.)

solubility

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

density

0.862 g/mL at 20 °C (lit.)

Quality Level

200

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Application

Piperidine may be employed as protective and structure-directing agent in the post synthesis of MCM (Mobil Composition of Matter)-49 zeolites.

General description

Piperidine can be prepared either by nickel catalyzed hydrogenation of pyridine or by cobalt catalyzed hydrogenolysis of tetrahydrofurylamine It forms adducts with α,β,γ,δ-tetraphenylporphyriniron(II) and protoporphyriniron(II). Mossbauer spectra of these adducts have been evaluated. It constitutes the skeleton of various alkaloids. Its chemical reactivity has been discussed.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

signalword

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

3 - Flammable liquids

wgk

WGK 1

flash_point_f

60.8 °F - closed cup

flash_point_c

16 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB7086
SDBB6816
0000484610
0000484610
SDBB6641

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Rubiralta M, et al.
Piperidine: Structure, Preparation, Reactivity, and Synthetic Applications of Piperidine and its Derivatives, 43, 2-2 (2013)
Alma Andersson et al.
Nature communications, 12(1), 6012-6012 (2021-10-16)
In the past decades, transcriptomic studies have revolutionized cancer treatment and diagnosis. However, tumor sequencing strategies typically result in loss of spatial information, critical to understand cell interactions and their functional relevance. To address this, we investigate spatial gene expression
Rubiralta M, et al.
Piperidine: Structure, Preparation, Reactivity, and Synthetic Applications of Piperidine and its Derivatives, 43, 14-14 (2013)
Rubiralta M, et al.
Piperidine: Structure, Preparation, Reactivity, and Synthetic Applications of Piperidine and its Derivatives, 43, 3-3 (2013)
Cristina Herencias et al.
Bio-protocol, 7(6), e2177-e2177 (2017-03-20)
Bdellovibrio bacteriovorus HD100 is an obligate predator that preys upon a wide variety of Gram negative bacteria. The biphasic growth cycle of Bdellovibrio includes a free-swimming attack phase and an intraperiplasmic growth phase, where the predator replicates its DNA and
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