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P58405

Sigma-Aldrich

3-Pyridinealdoxime

98%

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About This Item

Empirical Formula (Hill Notation):
C6H6N2O
CAS Number:
1193-92-6
Molecular Weight:
122.12
EC Number:
214-782-8
MDL number:
MFCD00006409
UNSPSC Code:
12352100
PubChem Substance ID:
24898713
NACRES:
NA.22

Assay

98%

form

powder

mp

150-153 °C (lit.)

SMILES string

[H]\C(=N/O)c1cccnc1

InChI

1S/C6H6N2O/c9-8-5-6-2-1-3-7-4-6/h1-5,9H/b8-5+

InChI key

YBKOPFQCLSPTPV-VMPITWQZSA-N

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - 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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

P58405-100G:
P58405-VAR:
P58405-BULK:
P58405-25G:

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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W L McPheat et al.
Journal of general microbiology, 128(11), 2681-2685 (1982-11-01)
3-Pyridine-carboxaldehyde and 3-pyridine-aldoxime were effective and specific inhibitors of the uptake of both nicotinic acid (NA) and nicotinamide (ND) by Bordetella pertussis, although neither compound inhibited the growth of the bacteria in liquid medium or the oxidation of glutamate by
Pavlína Nekvasilová et al.
Biochimica et biophysica acta. Proteins and proteomics, 1868(2), 140319-140319 (2019-11-20)
The β-N-acetylhexosaminidase from Penicillium oxalicum (PoHex; EC 3.2.1.52) is a fungal glycosidase with an outstandingly high GalNAcase/GlcNAcase activity ratio. It has a remarkable synthetic capability and can process carbohydrates functionalized at various positions. However, the production in the native fungal
Y Kato et al.
Applied and environmental microbiology, 66(6), 2290-2296 (2000-06-01)
The distribution of phenylacetaldoxime-degrading and pyridine-3-aldoxime-degrading ability was examined with intact cells of 975 microorganisms, including 45 genera of bacteria, 11 genera of actinomyces, 22 genera of yeasts, and 37 genera of fungi, by monitoring the decrease of the aldoximes

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