Carvedilol Impurity 6

Product Name Carvedilol Impurity 6
Alternate Names Carvedilol Impurities, Impurities of Carvedilol
CAT No. CS-P-02377
CAS No. 72956-35-5
Category Impurities
Stock IN-Stock
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Carvedilol
Therapeutic Anti-Hypertensives
Canonical Smiles CN(CCOC1=CC=CC=C1OC)CC(COC2=CC=CC3=C2C4=CC=CC=C4N3)O
InchIKey IIYAQEVCUAUADP-UHFFFAOYSA-N
Inchl InChI=1S/C25H28N2O4/c1-27(14-15-30-23-12-6-5-11-22(23)29-2)16-18(28)17-31-24-13-7-10-21-25(24)19-8-3-4-9-20(19)26-21/h3-13,18,26,28H,14-17H2,1-2H3
IUPAC 1-(9H-carbazol-4-yloxy)-3-[2-(2-methoxyphenoxy)ethyl-methylamino]propan-2-ol
Controlled No
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Carvedilol Impurity 6 is a byproduct that is formed during the manufacturing process of Carvedilol, a medication used to treat high blood pressure, heart failure, and other cardiovascular conditions. This impurity is a chemical compound that is structurally related to Carvedilol, but differs in its chemical composition due to the presence of an additional functional group. Carvedilol Impurity 6 is not intended for use in pharmaceutical applications, as it is considered a contaminant that can negatively affect the quality, safety, and efficacy of Carvedilol. The presence of this impurity in Carvedilol formulations can cause adverse effects on patients, such as allergic reactions, toxicity, or reduced effectiveness of the drug. The chemical formula of Carvedilol Impurity 6 is C24H34N2O4, and its molecular weight is 418.54 g/mol. It is a white to off-white crystalline powder that is insoluble in water, but soluble in organic solvents such as methanol, ethanol, and chloroform. The impurity can be detected and quantified using analytical techniques such as high-performance liquid chromatography (HPLC) or gas chromatography-mass spectrometry (GC-MS). In summary, Carvedilol Impurity 6 is a chemical byproduct that should be avoided in Carvedilol formulations due to its potential harmful effects on patients. Its chemical structure and properties can be analyzed using various analytical techniques, and its presence can be detected and quantified in pharmaceutical samples.

Related Compounds

Carvedilol Epoxide Impurity | Carvedilol Tetra(alkylpyrocatechol) Impurity | carvedilol impurity D acetate salt | N-Nitroso (carbazol) Carvedilol | Carvedilol EP Impurity A | Carvedilol Impurity D HCl salt | Carvedilol Impurity F | R)-(+)-5’-Hydroxyphenyl Carvedilol | N1-(2-chloroethyl)-N2-(((2-chloroethyl)amino)methyl)-N2-(2-((2,4-dimethylphenyl)thio)phenyl)ethane-1,2-diamine | Carvedilol Monoalkylpyrocatechol Impurity | Carvedilol Related Compound E | N-Nitroso Carvedilol | Carvedilol Dimer | Carvedilol Related Compound C | Carbazole | N-Isopropyl Carvedilol | Carvedilol Impurity 7 | N-formyl Carvedilol | Carvedilol EP Impurity A | Decarbazolyl Desmethyl Carvedilol | N-Nitroso Carvedilol S-Isomer | Carvedilol Carbonyl Impurity | Carvedilol 4-Hydroxy Carbazole Impurity | Carvedilol Bis(N-benzylalkylpyrocatechol) Impurity | N-Benzyl 6,7,8,9-Tetrahydro Carvedilol |

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