Levothyroxine EP Impurity F

Product Name Levothyroxine EP Impurity F
CAT No. CS-T-62058
CAS No. 911661-90-0
Category Impurities
Stock IN-Stock
Mol. Wt. 1120.76 g/mol
Mol. For. C₂₁H₁₃I₆NO₅
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Smileys O=C(O)[C@@H](N)CC1=CC(I)=C(OC2=CC(I)=C(OC3=CC(I)=C(O)C(I)=C3)C(I)=C2)C(I)=C1
Canonical Smiles C1=C(C=C(C(=C1I)OC2=CC(=C(C(=C2)I)OC3=CC(=C(C(=C3)I)O)I)I)I)CC(C(=O)O)N
InchIKey DBVHFBLWQRLBJN-KRWDZBQOSA-N
Inchl InChI=1S/C21H13I6NO5/c22-11-4-9(5-12(23)18(11)29)32-20-15(26)6-10(7-16(20)27)33-19-13(24)1-8(2-14(19)25)3-17(28)21(30)31/h1-2,4-7,17,29H,3,28H2,(H,30,31)/t17-/m0/s1
IUPAC (2S)-2-amino-3-[4-[4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodophenoxy]-3,5-diiodophenyl]propanoic acid
Controlled No
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Levothyroxine EP Impurity F is a chemical compound that is used in the production of levothyroxine, a medication that is used to treat hypothyroidism. Levothyroxine is a synthetic version of the thyroid hormone thyroxine, which is produced naturally by the thyroid gland. Hypothyroidism is a condition in which the thyroid gland does not produce enough thyroxine, resulting in symptoms such as fatigue, weight gain, and depression. Levothyroxine EP Impurity F is a byproduct of the synthesis of levothyroxine. It is classified as an impurity because it is not the desired end product, but it is present in small quantities in the final product. The chemical formula of Levothyroxine EP Impurity F is C15H11I4NO4, and its molecular weight is 776.97 g/mol. Levothyroxine EP Impurity F is typically removed from the final product through various purification methods, including chromatography and crystallization. The presence of impurities in pharmaceuticals is closely monitored by regulatory bodies such as the European Pharmacopoeia (EP), which sets standards for the purity and quality of medicines. In conclusion, Levothyroxine EP Impurity F is a chemical compound that plays a crucial role in the production of levothyroxine, a medication used to treat hypothyroidism. Although it is present in small quantities in the final product, its removal is essential to ensure the purity and quality of the medication.

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