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Sodium salicylate

SIAL/31493 - puriss. p.a., reag. Ph. Eur., 99.5-101.0% (calc. to the dried substance)

Synonym: 2-Hydroxybenzoic acid sodium salt; Salicylic acid sodium salt; Sodium 2-hydroxybenzoate

CAS Number: 54-21-7
Empirical Formula (Hill Notation): C7H5NaO3
Molecular Weight: 160.10
EC Number: 200-198-0
MDL Number: MFCD00002440
Linear Formula: HOC6H4COONa
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-31493-250G 250 g
$87.50
1/EA
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45-31493-1KG 1 kg
$208.00
1/EA
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agency reag. Ph. Eur.
  USP/NF
anion traces chloride (Cl-): ≤20 mg/kg
  sulfate (SO42-): ≤500 mg/kg
assay 99.5-101.0% (calc. to the dried substance)
cation traces Fe: ≤10 mg/kg
grade puriss. p.a.
impurities acidic reac. impurities, complies
  sulfite or thiosulfate, complies
  ≤0.001% heavy metals (as Pb)
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
loss ≤0.3% loss on drying, 105 °C
mp >300 °C (lit.)
Quality Level 100 
SMILES string [Na+].Oc1ccccc1C([O-])=O
suitability in accordance for appearance of solution
Application: Sodium salicylate may be used as phenolic reagent in salicylate method for the determination of ammonia. It may be employed as a hydrotropic agent to study the release of anticancer drug camptothecin (CPT) from the mixed micelles [composed of Pluronic P105 (P105) and D-α-tocopheryl polyethylene glycol 1000 succinate (TPGS)].
General description: Sodium salicylate can be prepared from the reaction of salicylic acid and ammonia. It exhibits fluorescence at higher concentrations and effectively absorbs β-particles. Due to these properties, it has been employed as fluor for the radioactivity detection in various gels.
Purity 99.5-101.0% (calc. to the dried substance)
mp >300 °C (lit.)
UNSPSC 12352100

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