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Description

Levodopa is an amino acid carrying a catechol ring, and that ring governs how the container is handled once it arrives. The sequence below is written as a store protocol rather than as a product description. See also our laboratory reagent: Fenyloalanina / L-Phenylalanine ≥ 99% 1000mg.

Step one: intake of the container

  1. Compare the label against the order: registry number 59-92-7, formula C9H11NO4, molar mass 197.19, net mass 1 g.
  2. Confirm that the certificate of analysis in the box carries the same batch number as the jar, and reject the delivery if it does not.
  3. Record appearance in the intake note; the material is described as a white crystalline solid, and any yellow or grey cast is written down before the jar is stored.
  4. Enter the batch into the reagent register with the delivery date, the retest date and the shelf location.
  5. File the safety data sheet in its current version alongside the certificate.

The appearance check is not cosmetic: a catechol is oxidation-prone, and darkening is the visible end of a process that has already changed the material. See also our catalogue listing: ALCAR / Acetyl-L-Carnitine – Purity ≥ 99% net weig.

Step two: control before release to a method

  1. Read which method produced the assay figure on the certificate, and whether the figure is chromatographic or titrimetric.
  2. Check that optical purity is addressed, either by specific rotation or by a chiral chromatographic determination, since the D form is a distinct article.
  3. Confirm that water content is reported separately from the assay.
  4. Confirm that residual solvents were tested against the manufacturing route rather than a generic list.
  5. Only then release the batch and note the release in the register with a signature.

Optical purity deserves the second position on that list. The two enantiomers share a formula, a mass and an ultraviolet spectrum, so a routine assay cannot separate them; only a chiral method or a polarimetric measurement can. A lot released without that line on the certificate is released on an assumption.

Step three: storage and each subsequent opening

  1. Store cool, dry and dark, in the original tightly closed container.
  2. Equilibrate a cold container to room temperature before opening, so that condensation does not settle on the crystals.
  3. Weigh promptly, reclose immediately and return the jar to its shelf position rather than leaving it on the bench.
  4. Note date, mass taken and the person taking it, one line per withdrawal.
  5. Inspect the remaining material at every opening and stop using the batch if the colour has shifted.

Water solubility is limited here, so working solutions are prepared fresh, and any solution that develops colour on standing is discarded rather than filtered: the colour is the reaction product itself.

Step four: closing the batch

  1. Record the final withdrawal and the residual mass.
  2. Dispose of the remainder through the chemical waste route, never through the sink.
  3. Keep the certificate, chromatograms and register entries after the jar is gone, for as long as the results derived from it are in use.

Other catalogue items

References

Animal and in vitro studies indexed in PubMed; no human-use guidance is provided here.

  • Nutt JG Pharmacokinetics and pharmacodynamics of levodopa 2008, Movement disorders : official journal of the. PMID 18781675
  • Klawans HL Levodopa-induced myoclonus 1975, Archives of neurology. PMID 1079721
  • Morris JG A review of some aspects of the pharmacology of levodopa 1978, Clinical and experimental neurology. PMID 386308
  • Goetz CG Influence of COMT inhibition on levodopa pharmacology and therapy 1998, Neurology. PMID 9591519

Reagent classification

It is not a substance for human use. It is not a veterinary product either. A high-purity laboratory product used in HPLC and GC-MS studies. Not a medicine, medical device or food product.

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