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Hyoscine Butylbromide EP Impurity E

Also known as: Hyoscine Butylbromide Impurities or impurities of Hyoscine Butylbromide
Chemical Name Hyoscine Butylbromide EP Impurity E
CAT No. CS-BX-00574
Status Prompt Dispatch
Category Impurities
Mol. Wt. 345.43 g/mol
Mol. For. C₂₀H₂₇NO₄
Hazardous This is a Hazardous Compound
COA View Sample COA

Additional Information


Controlled No
Parent API Hyoscine Butylbromide
Smileys O=C(O[C@H]1C[C@@]2([H])[C@]3([H])O[C@]3([H])[C@@](N2CCCC)([H])C1)[C@@H](C4=CC=CC=C4)CO
Hazardous Yes


Usage and description


Hyoscine Butylbromide EP Impurity E is a chemical compound that is used as an impurity reference standard for the analysis and identification of Hyoscine Butylbromide. Hyoscine Butylbromide is a medication that is used to relieve gastrointestinal tract spasms, as well as to reduce secretions in the respiratory tract. Hyoscine Butylbromide EP Impurity E is used in the pharmaceutical industry to ensure that the Hyoscine Butylbromide medication is of high quality and purity. The chemical formula of Hyoscine Butylbromide EP Impurity E is C22H32BrNO4S, and its molecular weight is 479.47 g/mol. It is a white to off-white powder that is soluble in water and organic solvents like methanol and ethanol. The compound is stable under normal storage conditions and has a shelf life of up to two years. Hyoscine Butylbromide EP Impurity E is synthesized by a multi-step synthesis process, which involves the use of various reagents and solvents. The compound is purified by chromatography and crystallization to obtain a high purity product. The impurity is characterized by various analytical techniques like HPLC, NMR, and MS to ensure its identity and purity. In conclusion, Hyoscine Butylbromide EP Impurity E is an important reference standard used in the pharmaceutical industry to ensure the quality and purity of Hyoscine Butylbromide medication. Its chemical properties and synthesis process make it an essential compound in the production of Hyoscine Butylbromide.

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