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71945

Sigma-Aldrich

Sodium salicylate

≥99.5% (HPLC), puriss. p.a.

Synonym(s):

2-Hydroxybenzoic acid sodium salt, Salicylic acid sodium salt, Sodium 2-hydroxybenzoate

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250 G
₪454.00
1 KG
₪1,437.00

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250 G
₪454.00
1 KG
₪1,437.00

About This Item

Linear Formula:
HOC6H4COONa
CAS Number:
54-21-7
Molecular Weight:
160.10
Beilstein:
3732792
EC Number:
200-198-0
MDL number:
MFCD00002440
UNSPSC Code:
12352107
PubChem Substance ID:
57652379
NACRES:
NA.21
Assay:
≥99.5% (HPLC)
form:
crystals
solubility:
water: 575.7 g/L at 25 °C (77 °F)

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grade

puriss. p.a.

Quality Level

200

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.[1][2]

Application

Sodium salicylate may be used as a reference standard for the quantification of the analyte in serum samples using an amperometric biosensor.[3]

Pictograms

Health hazardExclamation mark
GHS08,GHS07

Signal Word

Warning

Hazard Statements

H302,H319,H361d

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

208.9 °F - Pensky-Martens closed cup

Flash Point(C)

98.3 °C - Pensky-Martens closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF2915V
WXBF4228V
WXBF1467V
WXBD4819V
WXBD4193V

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Mosby's Pocket Dictionary of Medicine, Nursing & Health Professions - E-Book, 7 (2013)
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)
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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