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Cloforex is an anorectic of the amphetamine class. It is a prodrug to chlorphentermine.


Clonixin is a non-steroidal anti-inflammatory drug. It also has analgesic, antipyretic, and platelet-inhibitory actions. It is used primarily in the treatment of chronic arthritic conditions and certain soft tissue disorders associated with pain and inflammation.

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Codoxime is an opiate analogue that is a derivative of hydrocodone, where the 6-ketone group has been replaced by carboxymethyloxime. It has primarily antitussive effects and was found to have moderate potential to cause dependence in animal studies.


Cupreine is a crystalline alkaloid.It is occurs in cinchona bark and is closely related to quinine.It is used as an antimalarial agent.

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Cytidine is a nucleoside molecule that is formed when cytosine is attached to a ribose ring (also known as a ribofuranose) via a β-N1-glycosidic bond. Cytidine is a component of RNA.If cytosine is attached to a deoxyribose ring, it is known as a deoxycytidine.Dietary sources of cytidine include foods with high RNA (ribonucleic acid) contents such as organ meats, Brewer's yeast, as well as pyrimide-rich foods such as beer. During digestion, RNA-rich foods are broken-down into ribosyl pyrimidines (cytidine and uridine), which are absorbed intactIn humans, dietary cytidine is converted into uridine,which is probably the compound behind cytidine's metabolic effects.

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Dextrose is a simple sugar and an important carbohydrate in biology. Cells use it as the primary source of energy and a metabolic intermediate. It is one of the main products of photosynthesis and starts cellular respiration. It is a common medical analyte measured in blood samples. In industry, dextrose is used as a precursor to make vitamin C in the Reichstein process, to make citric acid, gluconic acid, bio-ethanol, polylactic acid, sorbitol.

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Dezocine is an opioid analgesic related to pentazocine, with a similar profile of effects that include analgesic action and euphoria at low doses, but produces dysphoria and hallucinations at high doses, most likely due to action at κ-opioid receptors. It has been found to be an effective painkiller comparable to meperidine, and so is a more effective analgesic than pentazocine, but causes relatively more respiratory depression than pentazocine. It is a useful drug for the treatment of pain, but side effects such as dizziness limit its clinical application, and it can produce opioid withdrawal syndrome in patients already dependent on other opioids. It is unusual among opioids as it is one of the only primary amines known to be an active opioid.

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Diazepam is a benzodiazepine with anticonvulsant, anxiolytic, sedative, muscle relaxant, and amnesic properties and a long duration of action. Its actions are mediated by enhancement of gamma-aminobutyric acid activity. It is used in the treatment of severe anxiety disorders, as a hypnotic in the short-term management of insomnia, as a sedative and premedicant, as an anticonvulsant, and in the management of alcohol withdrawal syndrome.Symptoms of Diazepam overdose include somnolence, confusion, coma, and diminished reflexes.

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Durolane is used in the treatment of osteoarthritis and is injected into the knee or hip joint to reduce pain and increase mobility. The majority of people affected by osteoarthritis (OA) are over the age of 40.

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Ebastine is a H1 antihistamine with low potential for causing drowsiness. It does not penetrate the blood–brain barrier to a significant amount and thus combines an effective block of the H1 receptor in peripheral tissue with a low incidence of central side effects, i.e. seldom causing sedation or drowsiness. Ebastine is a second-generation H1 receptor antagonist that is indicated mainly for allergic rhinitis and chronic idiopathic urticaria.

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