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Merck
CN

31493

Sodium salicylate

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

Synonym(s):

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

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About This Item

Linear Formula:
HOC6H4COONa
CAS Number:
Molecular Weight:
160.10
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
200-198-0
MDL number:
Beilstein/REAXYS Number:
3732792
Assay:
99.5-101.0% (calc. to the dried substance)
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Product Name

Sodium salicylate, puriss. p.a., reag. Ph. Eur., 99.5-101.0% (calc. to the dried substance)

Quality Segment

agency

USP/NF, reag. Ph. Eur.

grade

puriss. p.a.

assay

99.5-101.0% (calc. to the dried substance)

impurities

acidic reac. impurities, complies, sulfite or thiosulfate, complies, ≤0.001% heavy metals (as Pb)

loss

≤0.3% loss on drying, 105 °C

mp

>300 °C (lit.)

anion traces

chloride (Cl-): ≤20 mg/kg, sulfate (SO42-): ≤500 mg/kg

cation traces

Fe: ≤10 mg/kg

suitability

in accordance for appearance of solution

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

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.

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 mixed micelles.


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Warning

Hazard Classifications

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

Storage Class

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

ppe

dust mask type N95 (US), Eyeshields, Gloves



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