Tolterodine diol impurity

Product Name Tolterodine diol impurity
CAT No. CS-T-27966
CAS No. 851789-43-0
Category Impurities
Stock IN-Stock
Mol. Wt. 242.31 g/mol
Mol. For. C₁₆H₁₈O₂
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Purity 95%
Smileys CC1=CC(=C(C=C1)O)C(CCO)C2=CC=CC=C2
Canonical Smiles CC1=CC(=C(C=C1)O)C(CCO)C2=CC=CC=C2
InchIKey MJPIYYRDVSLOME-UHFFFAOYSA-N
Inchl InChI=1S/C16H18O2/c1-12-7-8-16(18)15(11-12)14(9-10-17)13-5-3-2-4-6-13/h2-8,11,14,17-18H,9-10H2,1H3
IUPAC 2-(3-hydroxy-1-phenylpropyl)-4-methylphenol
Controlled No
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Tolterodine diol impurity is a chemical compound that is commonly used in pharmaceutical research and development. It is a byproduct that is formed during the synthesis of tolterodine tartrate, which is a medication that is used to treat overactive bladder conditions. Tolterodine diol impurity is a colorless crystalline solid that has a molecular weight of 304.4 g/mol. It is soluble in organic solvents such as methanol and ethanol, but is only slightly soluble in water. Chemically, tolterodine diol impurity is a diol derivative of tolterodine. It is an impurity that is formed during the synthesis of tolterodine tartrate, which is a medication that is used to treat overactive bladder conditions. This impurity is typically present in small amounts in the final product, and its presence can affect the potency and purity of the medication. To ensure the quality and safety of tolterodine tartrate, it is important to control the level of tolterodine diol impurity in the final product. This is typically done through the use of analytical techniques such as high-performance liquid chromatography (HPLC), which can detect and quantify the impurity in the medication. In conclusion, tolterodine diol impurity is an important chemical compound that is used in the pharmaceutical industry. Its presence can affect the quality and potency of medications, and it is important to monitor its levels to ensure the safety and efficacy of pharmaceutical products.

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