56581
Perclorato de sodio monohydrate
suitable for HPLC, LiChropur™, 99.0-101.0% (T)
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Fórmula lineal:
NaClO4 · H2O
Número CAS:
Peso molecular:
140.46
UNSPSC Code:
41116105
NACRES:
NB.21
MDL number:
Servicio técnico
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Permítanos ayudarleQuality Segment
assay
99.0-101.0% (T)
form
solid
manufacturer/tradename
LiChropur™
technique(s)
HPLC: suitable
pH
4.5-8.0
solubility
H2O: 5%, clear, colorless
λ
10 % in water
UV absorption
λ: 210 nm Amax: ≤0.1, λ: 220 nm Amax: ≤0.05, λ: 230 nm Amax: ≤0.03, λ: 240 nm Amax: ≤0.02, λ: 500 nm Amax: ≤0.02
SMILES string
O.[Na+].[O-]Cl(=O)(=O)=O
InChI
1S/ClHO4.Na.H2O/c2-1(3,4)5;;/h(H,2,3,4,5);;1H2/q;+1;/p-1
InChI key
IXGNPUSUVRTQGW-UHFFFAOYSA-M
Application
Sodium perchlorate monohydrate along with acetonitrile may be used as a mobile phase in:
- Determination of methenamine, methenamine mandelate and methenamine hippurate in pharmaceutical preparations using ion-exchange high-performance liquid chromatography (HPLC).
- Development and validation of RP-HPLC method for the dissolution and assay of etoricoxib in pharmaceutical dosage forms.
- Determination of nitrate and nitrite by HPLC in human plasma.
Legal Information
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
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signalword
Danger
Clase de almacenamiento
5.1A - Strongly oxidizing hazardous materials
flash_point_f
Not applicable
flash_point_c
Not applicable
target_organs
Thyroid
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Ox. Sol. 1 - STOT RE 2
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Determination of nitrate and nitrite by high-performance liquid chromatography in human plasma
Jedlickova V, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 780(1), 193-197 (2002)
Development and validation of RP-HPLC method for the dissolution and assay of etoricoxib in pharmaceutical dosage forms
Singh B, et al.
International Journal of Pharmaceutical Quality Assurance, 6(01), 1-7 (2015)
Chiravi Pavitrapok et al.
Journal of pharmaceutical and biomedical analysis, 40(5), 1243-1248 (2005-11-22)
An ion-exchange column high-performance liquid chromatography (HPLC) method has been developed for the determination of methenamine in methenamine and methenamine hippurate pharmaceutical preparations. The HPLC method uses a Zorbax SCX-300 column with acetonitrile-0.1M sodium perchlorate monohydrate (pH 5.8) (70:30, v/v)