Ibrutinib Amino Piperidine dihydrochloride Impurity

Product Name Ibrutinib Amino Piperidine dihydrochloride Impurity
Alternate Names Ibrutinib Impurities, Impurities of Ibrutinib
CAT No. CS-ED-00984
CAS No. 1701403-10-2
Category Impurities
Stock IN-Stock
Mol. Wt. 459.37 g/mol
Mol. For. C₂₂H₂₄Cl₂N₆O
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Ibrutinib
Canonical Smiles C1CC(CNC1)N2C3=NC=NC(=C3C(=N2)C4=CC=C(C=C4)OC5=CC=CC=C5)N.Cl.Cl
InchIKey ZGTOUEKDPROJPB-UHFFFAOYSA-N
Inchl InChI=1S/C22H22N6O.2ClH/c23-21-19-20(15-8-10-18(11-9-15)29-17-6-2-1-3-7-17)27-28(22(19)26-14-25-21)16-5-4-12-24-13-16;;/h1-3,6-11,14,16,24H,4-5,12-13H2,(H2,23,25,26);2*1H
IUPAC 3-(4-phenoxyphenyl)-1-piperidin-3-ylpyrazolo[3,4-d]pyrimidin-4-amine;dihydrochloride
Controlled No
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Ibrutinib Amino Piperidine dihydrochloride Impurity is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard during the development and quality control of the drug Ibrutinib. Ibrutinib is a small molecule drug that is used to treat certain types of cancers, including mantle cell lymphoma and chronic lymphocytic leukemia. It works by inhibiting the enzyme Bruton's tyrosine kinase (BTK), which is essential for the growth and survival of cancer cells. The Ibrutinib Amino Piperidine dihydrochloride Impurity is a synthetic compound that is structurally similar to Ibrutinib. It is used as a reference standard during the development and quality control of Ibrutinib to ensure the purity and quality of the drug. The compound is produced by a series of chemical reactions that involve the use of various reagents and solvents. Chemically, Ibrutinib Amino Piperidine dihydrochloride Impurity is a piperidine derivative that contains a primary amino group. The compound is highly soluble in water and has a molecular weight of 317.2 g/mol. It is a white to off-white crystalline powder that is stable under normal storage conditions. In conclusion, Ibrutinib Amino Piperidine dihydrochloride Impurity is an important reference standard used in the development and quality control of Ibrutinib. It is a synthetic compound that is structurally similar to Ibrutinib and is highly soluble in water. Its use ensures the purity and quality of Ibrutinib, which is an important drug used in the treatment of certain types of cancers.

Related Compounds

ibrutinib acetyl impurity | Ibrutinib Di-piperidine impurity | Ibrutinib Impurity 12 | Ibrutinib impurity Dimer | N-Desacryloyl N-3-hydroxypropanoyl Ibrutinib | Ibrutinib Michael addition adduct | Ibrutinib Impurity 6 | Ibrutinib Impurity 1 | Rac -Ibrutinib propionaldehyde | N6-Acryloyl Ibrutinib | Ibrutinib Impurity 15 | Ibrutinib Impurity 9 | Ibrutinib impurity 25 | Ibrutinib N1-Oxide | Ibrutinib Hydroxy Impurity | Ibrutinib Impurity L | Ibrutinib Dimer | Ibrutinib Impurity 8 | Ibrutinib Impurity 7 | Ibrutinib (IBR) Diamine Impurity | N-Desacryloyl N-(3-Acryloyl-propanoyl) Ibrutinib | Ibrutinib Piperidine impurity | Ibrutinib Impurity 42 | Ibrutinib Impurity D | Ibrutinib Piperidine N-desacryl impurity | Ibrutinib N-Oxide impurity | N1-(2-Carboxyethyl) Ibrutinib |

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