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Merck
CN

688444

DL-2-Piperidine-d9 carboxylic acid

97 atom % D, 97% (CP)

Synonym(s):

DL-Pipecolic acid-(piperidine-d9)

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About This Item

Empirical Formula (Hill Notation):
C6D9H2NO2
Molecular Weight:
138.21
PubChem Substance ID:
UNSPSC Code:
12352005
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InChI

1S/C6H11NO2/c8-6(9)5-3-1-2-4-7-5/h5,7H,1-4H2,(H,8,9)/i1D2,2D2,3D2,4D2,5D

InChI key

HXEACLLIILLPRG-UHUJFCCWSA-N

SMILES string

[2H]C1([2H])NC([2H])(C(O)=O)C([2H])([2H])C([2H])([2H])C1([2H])[2H]

isotopic purity

97 atom % D

assay

97% (CP)

mp

272 °C (lit.)

mass shift

M+9

Packaging

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

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Warning

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Michael Hartmann et al.
Cell, 173(2), 456-469 (2018-03-27)
Following a previous microbial inoculation, plants can induce broad-spectrum immunity to pathogen infection, a phenomenon known as systemic acquired resistance (SAR). SAR establishment in Arabidopsis thaliana is regulated by the Lys catabolite pipecolic acid (Pip) and flavin-dependent-monooxygenase1 (FMO1). Here, we

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