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104051

Sigma-Aldrich

Picolinamide

98%

Synonym(s):

2-Pyridinecarboxamide

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About This Item

Empirical Formula (Hill Notation):
C6H6N2O
CAS Number:
1452-77-3
Molecular Weight:
122.12
EC Number:
215-921-5
MDL number:
MFCD00023483
UNSPSC Code:
12352100
PubChem Substance ID:
24846635
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

100

assay

98%

mp

110 °C (dec.) (lit.)

functional group

amide

SMILES string

NC(=O)c1ccccn1

InChI

1S/C6H6N2O/c7-6(9)5-3-1-2-4-8-5/h1-4H,(H2,7,9)

InChI key

IBBMAWULFFBRKK-UHFFFAOYSA-N

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Anti-ATR Antibody, clone 1B15 ZooMAb® Rabbit Monoclonal

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

biological source

rabbit

biological source

rabbit

biological source

rabbit

biological source

rabbit

clone

3L17, recombinant monoclonal

clone

1L17, recombinant monoclonal

clone

3D17, monoclonal, recombinant monoclonal

clone

1B15, recombinant monoclonal

antibody form

purified antibody

antibody form

purified antibody

antibody form

purified antibody

antibody form

purified antibody

species reactivity

human, rat, mouse

species reactivity

human, rat, mouse

species reactivity

human, mouse

species reactivity

human, rat, mouse

Gene Information

human ... RAB5A(5868)

Gene Information

-

Gene Information

-

Gene Information

-

Application

Picolinamide was used as template in preparation of molecular imprinting polymer[1]. Picolinamide was used in a study to evaluate kinetics and mechanism of liberation of picolinamide from chromium(III)-picolinamide complexes in HClO4[2].

Biochem/physiol Actions

Picolinamide is potential inhibitor of poly (ADP-ribose) synthetase of nuclei from rat pancreatic islet cells[3]. Picolinamide acts as bidentate ligand and forms complexes with lanthanide nitrates, thiocyanates and perchlorates[4].

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCP4017
MKCJ4117
MKCF5817
MKCC0588
MKBW7865V

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Protection by picolinamide, a novel inhibitor of poly (ADP-ribose) synthetase, against both streptozotocin-induced depression of proinsulin synthesis and reduction of NAD content in pancreatic islets.
H Yamamoto et al.
Biochemical and biophysical research communications, 95(1), 474-481 (1980-07-16)
Lanthanide complexes with picolinamide.
Condorelli G, et al.
J. Inorg. Nucl. Chem., 36(12), 3763-3766 (1974)
Ángel Manu Martínez et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(48), 11669-11676 (2017-06-22)
A practical picolinamide-directed C-H functionalization/alkyne annulation of benzylamine derivatives enabling access to the previously elusive 1,4-dihydroisoquinoline skeleton was developed using molecular O
Study properties of molecular imprinting polymer using a computational approach.
Wu L, et al.
Analyst, 128(7), 944-949 (2003)
Jason L Atkins et al.
Journal of the American Chemical Society, 134(33), 13546-13549 (2012-08-07)
Tris-arenes based on either isophthalic acid or 2,6-dipicolinic acid have been known for more than a decade to bind anions. Recent studies have also demonstrated their ability to transport various ions through membranes. In this report, we demonstrate two important
View All Related Papers

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