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Medronic acid

Cat No.:V31968 Purity: ≥98%
Medronic acid (Methylenediphosphonic acid) is a methylene-substituted diphosphonate.
Medronic acid
Medronic acid Chemical Structure CAS No.: 1984-15-2
Product category: New2
This product is for research use only, not for human use. We do not sell to patients.
Size Price Stock Qty
500mg
5g
Other Sizes
Official Supplier of:
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Product Description
Medronic acid (Methylenediphosphonic acid) is a methylene-substituted diphosphonate. Medronic acid has an affinity for and adheres to the surface of hydroxyapatite crystals in the bone matrix. Medronic acid accumulates at sites of osteoid mineralization and may be utilized in combination with radioactive isotopes in bone imaging.
Biological Activity I Assay Protocols (From Reference)
Toxicity/Toxicokinetics
Effects During Pregnancy and Lactation
◉ Overview of medication use during lactation The information in this record pertains to the use of technetium-99m methphosphonate (technetium-99m methylene bisphosphonate; technetium-99m MDP) as a diagnostic agent. A subcommittee of the U.S. Nuclear Regulatory Commission recommended that, for the sake of simplified guidance, breastfeeding should be discontinued for 24 hours after administration of all technetium-99m diagnostic products, although this interval may be longer than actually needed. [1] The International Commission on Radiological Protection also recommends that breastfeeding need not be interrupted after administration of technetium-99m methphosphonate. [2] However, in order to follow the principle of “minimizing exposure as much as possible,” some experts recommend breastfeeding the infant before administration and discontinuing breastfeeding 3 to 6 hours after administration, then completely expressing and discarding the milk. If the mother has expressed and stored breast milk before the examination, it can be fed to the infant during the breastfeeding interruption. [3-5] The mother does not need to avoid close contact with the infant after receiving a regular clinical dose. [6] Mothers concerned about the level of radioactivity in their breast milk can request testing at a hospital's nuclear medicine center. They can resume breastfeeding when the radioactivity level is within safe limits. A method for measuring the radioactivity in breast milk and determining when it is safe for a mother to resume breastfeeding has been published. [7] For breastfeeding mothers exposed to Tc-99m in the workplace, no additional precautions are required beyond general radiation protection measures. [8] ◉ Effects on breastfed infants
No relevant published information was found as of the revision date.
◉ Effects on lactation and breast milk
No relevant published information was found as of the revision date.
References

[1]. Salt Tolerance Enhancement of Liquid Chromatography-Matrix-Assisted Laser Desorption/Ionization-Mass Spectrometry Using Matrix Additive MethylenediphosphonicAcid. Mass Spectrom (Tokyo). 2014;3(1):A0031.

Additional Infomation
Medronic acid is a 1,1-bisphosphonate composed of methane substituted with two phosphonic acid groups. It plays a role in maintaining bone mineral density and chelating bone. Medronic acid is a methylene-substituted bisphosphonate. It has an affinity for hydroxyapatite crystals in the bone matrix and can adhere to their surface. The drug accumulates at sites of mineralization in osteoid tissue and can complex with radioactive isotopes (e.g., technetium-99m) for bone imaging. See also: Disodium medronic acid (salt form). Tetrasodium medronic acid (salt form).
1. Methylene diphosphonic acid (also known as methylene diphosphonic acid) is used as a matrix additive in liquid chromatography-matrix-assisted laser desorption/ionization mass spectrometry (LC-MALDI-MS) to improve the salt tolerance of the detection system [1]
2. Application of methylphosphonic acid in LC-MALDI-MS Experimental procedure: First, prepare a matrix solution containing methylphosphonic acid (as an additive) and conventional MALDI matrix; then, after separating the analyte by liquid chromatography, mix the eluent with the prepared matrix solution; next, spot the mixed solution onto a MALDI target plate; finally, perform mass spectrometry detection. Adding menadione acid can effectively reduce the interference of salt ions (such as sodium and potassium ions) in the sample on the ionization efficiency of the analyte, thereby improving the detection sensitivity and signal-to-noise ratio of the target compound in the salt-containing sample [1]. In the salt tolerance test of the detection system, compared with the traditional MALDI matrix without menadione acid, the LC-MALDI-MS system with menadione acid as the matrix additive can still maintain a stable detection signal when the sample salt concentration increases to 50 mM, while the traditional system shows a significant signal decay or even disappearance when the salt concentration is 10 mM [1].
These protocols are for reference only. InvivoChem does not independently validate these methods.
Physicochemical Properties
Molecular Formula
CH6O6P2
Molecular Weight
176.0023
Exact Mass
175.963
CAS #
1984-15-2
Related CAS #
25681-89-4 (di-hydrochloride salt);6145-29-5 (tetra-hydrochloride salt)
PubChem CID
16124
Appearance
White to off-white solid powder
Density
2.1±0.1 g/cm3
Boiling Point
583.2±60.0 °C at 760 mmHg
Melting Point
197-199 °C(lit.)
Flash Point
306.5±32.9 °C
Vapour Pressure
0.0±3.5 mmHg at 25°C
Index of Refraction
1.550
LogP
-4.11
Hydrogen Bond Donor Count
4
Hydrogen Bond Acceptor Count
6
Rotatable Bond Count
2
Heavy Atom Count
9
Complexity
152
Defined Atom Stereocenter Count
0
SMILES
P(C([H])([H])P(=O)(O[H])O[H])(=O)(O[H])O[H]
InChi Key
MBKDYNNUVRNNRF-UHFFFAOYSA-N
InChi Code
InChI=1S/CH6O6P2/c2-8(3,4)1-9(5,6)7/h1H2,(H2,2,3,4)(H2,5,6,7)
Chemical Name
phosphonomethylphosphonic acid
HS Tariff Code
2934.99.9001
Storage

Powder      -20°C    3 years

                     4°C     2 years

In solvent   -80°C    6 months

                  -20°C    1 month

Shipping Condition
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
Solubility Data
Solubility (In Vitro)
DMSO : ~250 mg/mL (~1420.45 mM)
Solubility (In Vivo)
Solubility in Formulation 1: ≥ 2.08 mg/mL (11.82 mM) (saturation unknown) in 10% DMSO + 40% PEG300 + 5% Tween80 + 45% Saline (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 20.8 mg/mL clear DMSO stock solution to 400 μL PEG300 and mix evenly; then add 50 μL Tween-80 to the above solution and mix evenly; then add 450 μL normal saline to adjust the volume to 1 mL.
Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH₂ O to obtain a clear solution.

Solubility in Formulation 2: ≥ 2.08 mg/mL (11.82 mM) (saturation unknown) in 10% DMSO + 90% (20% SBE-β-CD in Saline) (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 20.8 mg/mL clear DMSO stock solution to 900 μL of 20% SBE-β-CD physiological saline solution and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C,1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution.

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Solubility in Formulation 3: ≥ 2.08 mg/mL (11.82 mM) (saturation unknown) in 10% DMSO + 90% Corn Oil (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 20.8 mg/mL clear DMSO stock solution to 900 μL of corn oil and mix evenly.


 (Please use freshly prepared in vivo formulations for optimal results.)
Preparing Stock Solutions 1 mg 5 mg 10 mg
1 mM 5.6818 mL 28.4091 mL 56.8182 mL
5 mM 1.1364 mL 5.6818 mL 11.3636 mL
10 mM 0.5682 mL 2.8409 mL 5.6818 mL

*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.

Calculator

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An example of molarity calculation using the molarity calculator is shown below:
What is the mass of compound required to make a 10 mM stock solution in 5 ml of DMSO given that the molecular weight of the compound is 350.26 g/mol?
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  • The answer of 17.513 mg appears in the Mass box. In a similar way, you may calculate the volume and concentration.

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What volume of a given 10 mM stock solution is required to make 25 ml of a 25 μM solution?
Using the equation C1V1 = C2V2, where C1=10 mM, C2=25 μM, V2=25 ml and V1 is the unknown:
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  • The answer of 62.5 μL (0.1 ml) appears in the Volume (Start) box
g/mol

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Note: Chemical formula is case sensitive: C12H18N3O4  c12h18n3o4
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In vivo Formulation Calculator (Clear solution)
Step 1: Enter information below (Recommended: An additional animal to make allowance for loss during the experiment)
Step 2: Enter in vivo formulation (This is only a calculator, not the exact formulation for a specific product. Please contact us first if there is no in vivo formulation in the solubility section.)
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Calculation results

Working concentration mg/mL;

Method for preparing DMSO stock solution mg drug pre-dissolved in μL DMSO (stock solution concentration mg/mL). Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.

Method for preparing in vivo formulation:Take μL DMSO stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O,mix and clarify.

(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
             (2) Be sure to add the solvent(s) in order.

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