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180742

Sigma-Aldrich

4,4′-Bipiperidyl dihydrochloride

97%

Synonym(s):

4,4′-Bipiperidine dihydrochloride

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About This Item

Empirical Formula (Hill Notation):
C10H20N2 · 2HCl
CAS Number:
78619-84-8
Molecular Weight:
241.20
Beilstein:
3687878
EC Number:
278-958-6
MDL number:
MFCD00005998
UNSPSC Code:
12352100
PubChem Substance ID:
24850894
NACRES:
NA.22

Assay

97%

form

powder

mp

>300 °C (lit.)

SMILES string

Cl[H].Cl[H].C1CC(CCN1)C2CCNCC2

InChI

1S/C10H20N2.2ClH/c1-5-11-6-2-9(1)10-3-7-12-8-4-10;;/h9-12H,1-8H2;2*1H

InChI key

MQKBVVIPCLTENX-UHFFFAOYSA-N

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General description

4,4′-bipiperidine dihydrochloride is an intercalating agent.

Application

4,4′-Bipiperidyl dihydrochloride was used in the synthesis of organomodified montmorillonite (MMT) clay.
Reactant for synthesis of:
Isoreticular chemicals
Heterocyclic amide hydraphile synthetic cation transporters
Small molecules direct activators of Gi proteins
Vesamicol

Reactant for control of hydrogen bond network dimensionality in tetrachloroplatinate salts

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Felicity Massingberd-Mundy et al.
Scientific reports, 10(1), 17355-17355 (2020-10-17)
Affordable and readily available microelectronics are becoming prevalent in teaching laboratories however these useful and economic tools are not used widely in either academia or industry. Herein we report how a metal organic framework (MOF) synthetic route can be optimized
P Santhana Gopala Krishnan et al.
Journal of nanoscience and nanotechnology, 5(7), 1148-1157 (2005-08-20)
Polyimide-clay nanocomposites were prepared from their precursor, namely, polyamic acid, by the solution-casting method. Organomodified montmorillonite (MMT) clay was prepared by treating Na+MMT (Kunipia F) with three different intercalating agents, namely, piperazine dihydrochloride, 1,3-bis(4-piperidinylpropane) dihydrochloride and 4,4'-bipiperidine dihydrochloride at 80

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