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Butamirate Impurity 1

Also known as: Butamirate Impurities or impurities of Butamirate
Chemical Name Butamirate Impurity 1
CAT No. CS-P-00786
CAS Registry# 92321-53-4
Status Prompt Dispatch
Category Impurities
Mol. Wt. 219.32 g/mol
Mol. For. C₁₄H₂₁NO
Hazardous This is not a Hazardous Compound
COA View Sample COA

Additional Information


Controlled No
Parent API Butamirate
Smileys CCC(C1=CC=CC=C1)C(N(CC)CC)=O
Canonical Smiles CCC(C1=CC=CC=C1)C(=O)N(CC)CC
InchIKey MKMAIDOENHTYNN-UHFFFAOYSA-N
Inchl InChI=1S/C14H21NO/c1-4-13(12-10-8-7-9-11-12)14(16)15(5-2)6-3/h7-11,13H,4-6H2,1-3H3
IUPAC N,N-diethyl-2-phenylbutanamide
Hazardous No


Usage and description


Butamirate Impurity 1 is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard for the analysis of Butamirate citrate. Butamirate citrate is a cough suppressant medication that is commonly used to relieve dry coughs and other respiratory-related conditions. Butamirate Impurity 1 is a byproduct that is produced during the manufacturing process of Butamirate citrate, and it is important to ensure its purity and quality in order to maintain the efficacy and safety of the medication. The chemical formula of Butamirate Impurity 1 is C10H12O2, and its molecular weight is 164.20 g/mol. It is a white to off-white crystalline powder that is soluble in water and other polar solvents. Butamirate Impurity 1 is typically used as a reference standard in analytical methods such as high-performance liquid chromatography (HPLC), gas chromatography (GC), and mass spectrometry (MS). In pharmaceutical manufacturing, the purity of Butamirate Impurity 1 is critical to ensure the safety and efficacy of the final product. The impurity can affect the quality of the drug product, and may even have potential health risks for patients. Therefore, it is important for manufacturers to closely monitor the purity of Butamirate Impurity 1 during the production process to ensure the quality of the final product.

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