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84230

Sigma-Aldrich

Salicylamide

puriss., ≥99.0% (T)

Sinónimos:

2-Hydroxybenzamide

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About This Item

Fórmula lineal:
2-(HO)C6H4CONH2
Número de CAS:
65-45-2
Peso molecular:
137.14
Beilstein/REAXYS Number:
742439
EC Number:
200-609-3
MDL number:
MFCD00007978
UNSPSC Code:
12352100
PubChem Substance ID:
329769292
NACRES:
NA.22

grade

puriss.

Quality Level

100

assay

≥99.0% (T)

form

solid

mp

139-141 °C
140-144 °C (lit.)

solubility

methanol: 0.1 g/mL, clear

SMILES string

NC(=O)c1ccccc1O

InChI

1S/C7H7NO2/c8-7(10)5-3-1-2-4-6(5)9/h1-4,9H,(H2,8,10)

InChI key

SKZKKFZAGNVIMN-UHFFFAOYSA-N

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
BCCG6984
BCCD6002
BCCD1842
BCBZ6061
BCBZ3536

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S Zhang et al.
Transplantation proceedings, 38(5), 1247-1252 (2006-06-27)
Cardiac ischemia/reperfusion (I/R) injury, a necessary consequence of transplantation, is probably related to the formation of reactive oxygen species (ROS). The ROS burst within the first moments of reperfusion is associated with injury, continuously generate O2- at about 3% to
Stephanie S Barnes et al.
Dalton transactions (Cambridge, England : 2003), 40(17), 4707-4714 (2011-03-25)
Addition of boranes to N-aryl-salicylaldimines takes place initially at the reactive phenolic O-H bond to give an activated boron-containing imine and dihydrogen. In some cases a subsequent intramolecular hydrogenation step is observed and the C=N imine bond is reduced to
R Dolezal et al.
European journal of medicinal chemistry, 44(2), 869-876 (2008-06-13)
Quantitative relationships between the molecular structure and the biological activity of 49 isosteric salicylamide derivatives as potential antituberculotics with a new mechanism of action against three Mycobacterial strains were investigated. The molecular structures were represented by quantum chemical B3LYP/6-31G( *)
Silvia Wein et al.
Xenobiotica; the fate of foreign compounds in biological systems, 42(5), 477-482 (2011-12-23)
We investigated acute effects and effects after chronic intake of the orally administered flavonol quercetin on pharmacokinetics of salicylamide metabolites (SAM) after oral administration of salicylamide in pigs. Salicylamide (8 mg/kg body weight) was orally administered to seven pigs either
J A Murillo Pulgarín et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 79(5), 909-914 (2011-05-13)
A new methodology for the simultaneous determination of salicylic acid and salicylamide in biological fluids is proposed. The strong overlapping of the fluorescence spectra of both analytes makes impossible the conventional fluorimetric determination. For that reason, the use of fluorescence
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