4-[3-(Dibutylamino)propoxy]benzoic Acid-d6 Hydrochloride

Product Name 4-[3-(Dibutylamino)propoxy]benzoic Acid-d6 Hydrochloride
CAT No. CS-T-88399
CAS No. 1329808-49-2
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Smileys CCCCN(CCCC)CCCOC1=CC=C(C=C1)C(=O)O.Cl
Canonical Smiles CCCCN(CCCC)CCCOC1=CC=C(C=C1)C(=O)O.Cl
InchIKey HEXBWGNCINCLCP-XVDDJZHLSA-N
Inchl InChI=1S/C18H29NO3.ClH/c1-3-5-12-19(13-6-4-2)14-7-15-22-17-10-8-16(9-11-17)18(20)21;/h8-11H,3-7,12-15H2,1-2H3,(H,20,21);1H/i7D2,14D2,15D2;
IUPAC 4-[1,1,2,2,3,3-hexadeuterio-3-(dibutylamino)propoxy]benzoic acid;hydrochloride
Controlled No
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4-[3-(Dibutylamino)propoxy]benzoic Acid-d6 Hydrochloride is a deuterated form of the chemical compound which is used in the pharmaceutical industry as a tracer in drug metabolism studies. This compound is made by introducing deuterium atoms into the structure of the molecule, which makes it an ideal candidate for use in metabolic studies since it can be easily traced in biological systems. The chemical formula of 4-[3-(Dibutylamino)propoxy]benzoic Acid-d6 Hydrochloride is C16H22D6NO3.HCl, and it has a molecular weight of 341.87 g/mol. The compound has a melting point of 190-195°C and is soluble in water and organic solvents such as methanol, ethanol, and acetone. The compound is also used in research studies to investigate the effects of different drugs on human metabolism. It is known to inhibit the activity of certain cytochrome P450 enzymes which play a crucial role in drug metabolism. Therefore, 4-[3-(Dibutylamino)propoxy]benzoic Acid-d6 Hydrochloride can be used to study the metabolism of drugs that are metabolized by these enzymes. In conclusion, 4-[3-(Dibutylamino)propoxy]benzoic Acid-d6 Hydrochloride is a useful compound in drug metabolism studies and research investigations. Its deuterated form allows for easy tracing in biological systems, making it an ideal candidate for use in metabolic studies.

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