1,2-Diphenylethane-d14
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1,2-Diphenylethane-d14 is the d14-labeled Bibenzyl (HY-78004). Bibenzyl (s-Diphenylethane; Dibenzyl) is the parent core structure of bibenzyl-type natural products and an intermediate in organic synthesis. Hydroxyl-substituted derivatives of Bibenzyl are mainly isolated from plants such as Dendrobium (Orchidaceae) and Cannabaceae. These derivatives accumulate when plants are exposed to fungal infection and biotic stress, and exhibit antioxidant, anti-inflammatory, and anti-hepatic steatosis activities.
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- Pureté : 99.5%
- CAS No.: 94371-89-8
- Formule: C14D14
- Masse moléculaire:196.35
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Stockage:Powder -20°C, 3 years ; In solvent -80°C, 6 months , -20°C, 1 month
Activité biologique
Description
In Vitro
Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Application
1. This compound can be used as a tracer
2. This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Chemical Information
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CAS No. 94371-89-8
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Unlabeled CAS 103-29-7
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Appearance Crystal
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Masse moléculaire 196.35
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Formule C14D14
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Color White to off-white
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SMILES
[2H]C1=C([2H])C([2H])=C([2H])C([2H])=C1C([2H])([2H])C([2H])([2H])C2=C([2H])C([2H])=C([2H])C([2H])=C2[2H]
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
Powder -20°C 3 years In solvent -80°C 6 months -20°C 1 month
Pureté et documentation
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Fiche technique (284 KB)
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SDS (251 KB)
- English - EN (251 KB)
- Français - FR (251 KB)
- Deutsch - DE (251 KB)
- Norwegian - NO (251 KB)
- Español - ES (251 KB)
- Swedish - SV (251 KB)
- Italian - IT (251 KB)
- Korean - KR (251 KB)
- Portuguese - PT (251 KB)
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Instruction de manipulation (2659 KB)
Références
[2]. Zhang ZM, et al. Bibenzyl and naphthalene derivatives from Dendrobium chrysanthum and their anti-hepatic-steatosis activities. Bioorganic chemistry. 2024 Apr;145:107236. [Content Brief]
[3]. Boddington KF, et al. Bibenzyl synthesis in Cannabis sativa L. Plant J. 2022 Feb;109(3):693-707. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)