For research use only. Not for therapeutic Use.
Bisphenol AP-d5 is an isotopically labeled version of bisphenol AP, which is a derivative of bisphenol A known for its use in the synthesis of high-performance polymers and resins. This compound is enhanced with five deuterium atoms, making it an essential tool for advanced analytical studies. The deuterium labeling improves its detection and quantification in complex matrices using mass spectrometry and nuclear magnetic resonance (NMR) techniques. Bisphenol AP-d5 is crucial for research in polymer science, particularly for studying the kinetics and mechanisms of polymerization processes, as well as the environmental impact and degradation pathways of bisphenol derivatives. Its use facilitates more accurate and reliable scientific investigations in materials science and environmental studies.
Catalog Number | R028689 |
CAS Number | NA |
Synonyms | 1,1-Bis(4-hydroxyphenyl)-1-phenylethane-d5; 1-Phenyl-1,1-bis(4-hydroxyphenyl)ethane-d5; 4,4’-(1-Phenylethylidene)bisphenol-d5; 4,4’-(1-Phenylethylidene)diphenol-d5; 4,4’-(α-Methylbenzylidene)diphenol-d5; Bis(4-hydroxyphenyl)methylphenylmethane-d5; Bi |
Molecular Formula | C₂₀H₁₃D₅O₂ |
Purity | ≥95% |
Storage | Store at -20C |
IUPAC Name | 4-[1-(4-hydroxyphenyl)-1-(2,3,4,5,6-pentadeuteriophenyl)ethyl]phenol |
InChI | InChI=1S/C20H18O2/c1-20(15-5-3-2-4-6-15,16-7-11-18(21)12-8-16)17-9-13-19(22)14-10-17/h2-14,21-22H,1H3/i2D,3D,4D,5D,6D |
InChIKey | VOWWYDCFAISREI-VIQYUKPQSA-N |
SMILES | [2H]C1=C(C(=C(C(=C1[2H])[2H])C(C)(C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)[2H])[2H] |