Etidronic acid
Systematic (IUPAC) name | |
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(1-hydroxyethan-1,1-diyl)bis(phosphonic acid) | |
Clinical data | |
AHFS/Drugs.com | International Drug Names |
Licence data | US FDA:link |
Pregnancy category |
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Legal status |
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Routes of administration | Oral, intravenous |
Pharmacokinetic data | |
Bioavailability | 3% |
Metabolism | Nil |
Biological half-life | 1 to 6 hours |
Excretion | Renal and fecal |
Identifiers | |
CAS Number | 2809-21-4 |
ATC code | M05BA01 M05BB01 |
PubChem | CID 3305 |
IUPHAR/BPS | 7184 |
DrugBank | DB01077 |
ChemSpider | 3189 |
UNII | M2F465ROXU |
KEGG | D02373 |
ChEBI | CHEBI:4907 |
ChEMBL | CHEMBL871 |
Chemical data | |
Formula | C2H8O7P2 |
Molar mass | 206.028 g/mol |
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Etidronic acid (INN) or 1-hydroxyethane 1,1-diphosphonic acid (HEDP) is a bisphosphonate used in detergents, water treatment, cosmetics and pharmaceutical treatment.
An etidronate is a salt of etidronic acid, abbreviated MnHEDP (M: is a cation, n: number of M maximum 4).
Chelating Agent and Anti-oxidant
Etidronic acid is a chelating agent and may be added to bind or, to some extent, counter the effects of substances, such as calcium, iron or other metal ions, which may be discharged as a component of grey wastewater and could conceivably contaminate groundwater supplies. As a phosphonate it has corrosion inhibiting properties on unnalloyed steel. Etidronic acid also acts to retard rancidification and oxidation of fatty acids.
HEDP and its salts are added to detergents and other cleaning agents to prevent the effects of hard water. It is also used in peroxide bleaching to prevent degradation of peroxides by transition metals.
Etidronic acid is listed as an ingredient of several cosmetic formulations where it is used for suppressing radical formation, emulsion stabiliser and viscosity control. While etidronic acid has not been limited from inclusion in cosmetics and does have legitimate uses, it is recommended that, as with most cosmetic products (particularly soaps), the product should be thoroughly rinsed from the skin after use.
Etidronic acid is also included among swimming pool chemicals. It is used as a stain inhibitor to prevent metal ions coming out of solution and staining the sides of swimming pools.
Synthesis
Etidronic acid can be prepared by reaction of Phosphorus trichloride with acetic acid in a tertiary amine, or by reaction of an acetic acid/acetic anhydride mixture with phosphorous acid.[1]
Use
Pharmaceutical
Etidronic acid (Didronel ®) is a bisphosphonate used to strengthen bone, treat osteoporosis, and treat Paget's disease of bone.
Bisphosphonates primarily reduce osteoclastic activity, which prevents bone resorption, and thus moves the bone resorption/formation equilibrium toward the formation side and hence makes bone stronger on the long run. Etidronate, unlike other bisphosphonates, also prevents bone calcification. For this reason, other bisphosphonates, like alendronate, are preferred when fighting osteoporosis. To prevent bone resorption without affecting too much bone calcification, etidronate must be administered only for a short time once in a while, for example for two weeks every 3 months. When given on a continuous basis, say every day, etidronate will altogether prevent bone calcification. This effect may be useful and etidronate is in fact used this way to fight heterotopic ossification. But in the long run, if used on a continuous basis, it will cause osteomalacia.
Chemical
HEDP is used as scale and corrosion inhibition in circulating cool water system, oil field and low-pressure boilers in fields such as electric power, chemical industry, metallurgy, fertilizer, etc. In light woven industry, HEDP is used as detergent for metal and nonmetal. In dyeing industry, HEDP is used as peroxide stabilizer and dye-fixing agent; In non-cyanide electroplating, HEDP is used as chelating agent. The dosage of 1–10 mg/L is preferred as scale inhibitor, 10–50 mg/L as corrosion inhibitor, and 1000–2000 mg/L as detergent. Usually, HEDP is used together with polycarboxylic acid.
References
- ↑ "Compound Summary for CID 3305", pubchem.ncbi.nlm.nih.gov, Use and manufacturing, retrieved Jan 2015
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