Basic information Safety Supplier Related

ALPHA-NAPHTHYL PHOSPHATE DISODIUM SALT

Basic information Safety Supplier Related

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
Mol File:
2183-17-7.mol
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ALPHA-NAPHTHYL PHOSPHATE DISODIUM SALT Chemical Properties

Melting point:
>300°C
storage temp. 
-20°C
BRN 
4895811
CAS DataBase Reference
2183-17-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
10-21

MSDS

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ALPHA-NAPHTHYL PHOSPHATE DISODIUM SALT Usage And Synthesis

Uses

1-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 Methods

Purify 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.]

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