Skip to Content
Merck

P62208

3-Pyridinecarboxaldehyde

98%

Synonym(s):

Nicotinaldehyde

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C6H5NO
CAS Number:
500-22-1
Molecular Weight:
107.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24898656
EC Number:
207-900-4
Beilstein/REAXYS Number:
105343
MDL number:
MFCD00006382
Assay:
98%

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

3-Pyridinecarboxaldehyde, 98%

InChI key

QJZUKDFHGGYHMC-UHFFFAOYSA-N

InChI

1S/C6H5NO/c8-5-6-2-1-3-7-4-6/h1-5H

SMILES string

[H]C(=O)c1cccnc1

assay

98%

refractive index

n20/D 1.549 (lit.)

bp

78-81 °C/10 mmHg (lit.)

density

1.141 g/mL at 20 °C (lit.)

storage temp.

2-8°C

Quality Level

200

Looking for similar products? Visit Product Comparison Guide

Related Categories

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Flam. Liq. 3 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

95.0 °F - closed cup

flash_point_c

35 °C - closed cup

ppe

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SDBB5847
0000114508
0000114507
0000087263
0000087251

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

[Selenazoles. IX. [9]. 3-methyl-4-R-selenazolidene-2-hydrazones of acetaldehyde, benzaldehyde, isonicotinaldehyde, nicotinaldehyde and picolinaldehyde].
S Biliński et al.
Annales Universitatis Mariae Curie-Sklodowska. Sectio D: Medicina, 39, 25-31 (1984-01-01)
P Narender et al.
Bioorganic & medicinal chemistry letters, 15(24), 5378-5381 (2005-10-11)
New Baylis-Hillman adducts are synthesized based on substituted 2-chloronicotinaldehydes and screened for their in vitro anti-malarial activity against chloroquine sensitive and chloroquine resistant Plasmodium falciparum. Out of the six new compounds synthesized and screened, 2b, 2c and 2d compounds showed
K S De Jongh et al.
The Biochemical journal, 242(1), 143-150 (1987-02-15)
The kinetic mechanism of the major sheep liver aldehyde reductase (ALR1) was studied with three aldehyde substrates: p-nitrobenzaldehyde, pyridine-3-aldehyde and D-glucuronate. In each case the enzyme mechanism was sequential and product-inhibition studies were consistent with an ordered Bi Bi mechanism
Sujin P Jose et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 64(1), 205-209 (2006-03-18)
The Fourier transform Raman and infrared spectra of nicotinaldehyde were recorded and the observed frequencies were assigned to various modes of vibration in terms of fundamentals by assuming Cs point group symmetry. A normal coordinate analysis was also carried out
Hugo Destaillats et al.
Environmental science & technology, 40(6), 1799-1805 (2006-03-31)
Assessment of secondhand tobacco smoke exposure using nicotine as a tracer or biomarker is affected by sorption of the alkaloid to indoor surfaces and by its long-term re-emission into the gas phase. However, surface chemical interactions of nicotine have not
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service