Phenolphthalein monophosphate, bis(cyclohexylammonium) salt CAS: 14815-59-9
MF: C20H15O7P•2(C6H13N)
MW: 596.65
An indicator for various titrations.
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Phenolphthalein monophosphate, bis(cyclohexylammonium) salt (CAS 14815-59-9)

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Alternate Names: Cyclohexanaminium 4-(1-(4-hydroxyphenyl)-3-oxo-1,3-dihydroisobenzofuran-1-yl)phenyl phosphate
Application Phenolphthalein monophosphate, bis(cyclohexylammonium) salt is an indicator for various titrations
CAS 등록번호: 14815-59-9
순도: ≥91%
분자량: 596.65
분자식: C20H15O7P•2(C6H13N)
연구용으로만 사용가능합니다. 진단이나 치료용으로 사용불가합니다.
* Refer to Certificate of Analysis for lot specific data (including water content).

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Phenolphthalein monophosphate, bis(cyclohexylammonium) salt is a substrate for alkaline phosphatase, which acts as an indicator in various titrations and enzyme immunoassays. In addition, Phenolphthalein monophosphate, bis(cyclohexylammonium) salt can be indirectly used to label hormones via tagging the hormones with different enzymes such as alkaline phosphatase which will react with Phenolphthalein monophosphate, bis(cyclohexylammonium) salt. Alternate studies show that Phenolphthalein monophosphate, bis(cyclohexylammonium) salt can enhance bioautography with Trichomonas vaginalis. Another study indicates that Phenolphthalein monophosphate, bis(cyclohexylammonium) salt can distinguish between various acid phosphatase isoenzymes.


References

1. Sparkers, M.C., et al. 1975. Anal. Biochem. 64: 316-318. PMID: 49157
2. Blake, C., et al. 1982. Clin. Chem. 28: 1469-1473. PMID: 7044615
3. Parkash, O., et al. 1986. Clin. Chem. 32: 894. PMID: 3754497
4. Roberts, I.M., et al. 1991. J. Immunol. Methods. 143: 49-56. PMID: 1919036

Appearance :
Powder
Physical State :
Solid
용해도 :
Soluble in water, and methanol (10 mg/ml).
저장 :
Store at -20° C
비등점 :
793.4° C at 760 mmHg (Predicted)
굴절률 :
n20D ~1.69 (Predicted)
연구용으로만 사용가능합니다. 진단이나 치료용으로 사용불가합니다.
WGK Germany :
3
PubChem CID :
45489981
MDL Number :
MFCD00070132
EC Number :
238-884-7
SMILES :
C1CCC(CC1)[NH3+].C1CCC(CC1)[NH3+].C1=CC=C2C(=C1)C(=O)OC2(C3=CC=C(C=C3)O)C4=CC=C(C=C4)OP(=O)([O-])[O-]

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