ALPHA-NAPHTHYL PHOSPHATE DISODIUM SALT

ALPHA-NAPHTHYL PHOSPHATE DISODIUM SALT
  • CAS No.:2183-17-7
Other grades of this product :
ALPHA-NAPHTHYL PHOSPHATE DISODIUM SALT Basic information
Product Name:ALPHA-NAPHTHYL PHOSPHATE DISODIUM SALT
Synonyms:1-NAPHTHYLPHOSPHORIC ACID DISODIUM SALT;1-NAPHTHYL PHOSPHATE DISODIUM SALT;1-NAPHTHYL DISODIUM ORTHOPHOSPHATE;1-NAPHTHALENOL DIHYDROGEN PHOSPHATE DISODIUM SALT;PHOSPHORIC ACID 1-NAPHTHYL ESTER DISODIUM SALT;SODIUM A-NAPHTHYL ACID PHOSPHATE (DISODIUM);ALPHA-NAP-PHOS 2NA;ALPHA-NAPHTHYL PHOSPHATE DISODIUM SALT
CAS:2183-17-7
MF:C10H10NaO4P
MW:248.15
EINECS:218-564-3
Product Categories:
Mol File:2183-17-7.mol
ALPHA-NAPHTHYL PHOSPHATE DISODIUM SALT Chemical Properties
Melting point >300°C
storage temp. -20°C
BRN 4895811
CAS DataBase Reference2183-17-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
10-21
MSDS Information
ProviderLanguage
SigmaAldrich English
ALPHA-NAPHTHYL PHOSPHATE DISODIUM SALT Usage And Synthesis
Uses1-Naphthyl phosphate disodium salt has been used:
  • as a component in the mixture for soaking the chromatography paper for determining acid phosphatase activity
  • in the staining of the alkaline phosphatase isoforms in 7.5% non-denaturing polyacrylamide gel
  • as a component in the mixture for soaking the chromatography paper for preparing acid phosphomonoesterase-reactive imprinting sheets
  • as a component in the staining solution for staining the roots for determining phosphomonoesterase activity
Purification MethodsPurify the salt through an acid ion-exchange column (in H+ form) to give the free acid [1136-89-6], M 224.2, which is obtained by freeze drying and recrystallising from Me2CO/*C6H6, or by adding 2.5volumes of hot CHCl3 (or 20 parts of boiling *C6H6) to a hot solution of 1 part acid and 1.2 parts Me2CO and cooling (m 155-157o, 157-158o). The acid is dissolved in the minimum volume of H2O to which 2 equivalents of NaOH are added and then freeze dried, or by adding the equivalent amount of MeONa in MeOH to a solution of the acid in MeOH and collecting the Na salt, washing with cold MeOH, then Et2O, and drying in a vacuum. [Friedman & Seligman J Am Chem Soc 72 624 1950, Chanley & Feageson J Am Chem Soc 77 4002 1955.] The monosodium salt [1136-89-6] is similarly prepared but by using 1 equivalent of NaOH. The phosphate group is hydrolysed at pH 1.1-5.85 at 70o. [Beilstein 6 IV 4226.] It is a substrate for alkaline phosphatase [Gomori Methods Enzymol 4 381 1957, 128 212 1968], and prostatic phosphatase [Babson Clin Chem 30 1418 1984]. [See p 538 in “Metal-organic Compounds”, Chapter 5, Beilstein 6 IV 4226.]
ALPHA-NAPHTHYL PHOSPHATE DISODIUM SALT Preparation Products And Raw materials

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