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Merck

71945

Sigma-Aldrich

Salicilato de sodio

≥99.5% (HPLC), puriss. p.a.

Sinónimos:

2-Hidroxibenzoato de sodio, Ácido 2-hidroxibenzoico sodium salt, Ácido salicílico sodium salt

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About This Item

Fórmula lineal:
HOC6H4COONa
Número de CAS:
Peso molecular:
160.10
Beilstein/REAXYS Number:
3732792
EC Number:
MDL number:
UNSPSC Code:
12352107
PubChem Substance ID:
NACRES:
NA.21

grade

puriss. p.a.

Quality Level

assay

≥99.5% (HPLC)

form

crystals

loss

≤0.5% loss on drying, 110 °C

color

white

useful pH range

6.85 (26.3 °C)

mp

>300 °C (lit.)

solubility

water: 575.7 g/L at 25 °C (77 °F)

anion traces

chloride (Cl-): ≤100 mg/kg
sulfate (SO42-): ≤600 mg/kg

cation traces

Ca: ≤50 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤10 mg/kg
K: ≤50 mg/kg
Mg: ≤25 mg/kg
Mn: ≤5 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤25 mg/kg

SMILES string

[Na+].Oc1ccccc1C([O-])=O

InChI

1S/C7H6O3.Na/c8-6-4-2-1-3-5(6)7(9)10;/h1-4,8H,(H,9,10);/q;+1/p-1

InChI key

ABBQHOQBGMUPJH-UHFFFAOYSA-M

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General description

Sodium salicylate belongs to the class of nonacetylated salicylates.

Application

Sodium salicylate may be used as a reference standard for the quantification of the analyte in serum samples using an amperometric biosensor.

pictograms

Health hazardExclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Repr. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

208.9 °F - Pensky-Martens closed cup

flash_point_c

98.3 °C - Pensky-Martens closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Determination of salicylate in blood serum using an amperometric biosensor based on salicylate hydroxylase immobilized in a polypyrrole?glutaraldehyde matrix
Junior RL, et al.
Talanta, 51(3), 547-557 (2000)
Mosby's Pocket Dictionary of Medicine, Nursing & Health Professions - E-Book, 7 (2013)
Handbook of Drug Interactions: A Clinical and Forensic Guide (2003)
Kui Wang et al.
Journal of medicinal chemistry, 52(20), 6402-6412 (2009-10-16)
Viologens are showing an increasing number of scientific and technical applications in addition to their use as herbicides. However, their high toxicity poses considerable risks to human health, society, and the environment. In this context, we propose a new therapeutic
Rainer Amann et al.
European journal of pharmacology, 447(1), 1-9 (2002-07-11)
Aspirin (acetylsalicylic acid) is one of the most widely used drugs worldwide. It acetylates cyclooxygenases thereby irreversibly blocking the conversion of arachidonic acid to prostanoids. Biotransformation of aspirin yields salicylate, a compound that possesses similar anti-inflammatory potency as aspirin but

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