3-Heptanol-d4
3-Heptanol-d4 (Butylethylcarbinol-d4) is the deuterium labeled 3-Heptanol (HY-134058). 3-Heptanol is a biotransformation product of n-heptane. 3-Heptanol can act as the building block in the synthesis of 4-(3-adamantan-1-yl-ureido)-butyric acid and cyclohexanecarboxylic acid derivatives as sEH inhibitors. 3-Heptanol can be used as a solvent to form microenvironments around single-walled carbon nanotubes. 3-Heptanol can be used in the preperation of substituted pyrimidine derivatives as C1 domain-targeted isophthalate analogs to study their binding affinities towards PKCα isoform.
For research use only. We do not sell to patients.
- Formula: C7H12D4O
- Molecular Weight:120.23
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Biological Activity
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Chemical Information
- Purity & Documentation
- References
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Help & FAQs
Biological Activity
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.
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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Unlabeled Cas 589-82-2
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Molecular Weight 120.23
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Formula C7H12D4O
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SMILES
CC([2H])([2H])C(O)C([2H])([2H])CCC
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Synonyms
Butylethylcarbinol-d4
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
[1]. Perbellini L, et al., Identification of the n-heptane metabolites in rat and human urine. Arch Toxicol. 1986 Apr;58(4):229- [Content Brief]
[2]. Kim IH, et al., Biologically active ester derivatives as potent inhibitors of the soluble epoxide hyhdrolase. Bioorg Med Chem Lett. 2012 Sep 15;22(18):5889-92. [Content Brief]
[3]. Silvera-Batista CA, et al., Solvatochromic shifts of single-walled carbon nanotubes in nonpolar microenvironments. Phys Chem Chem Phys. 2010 Jul 14;12(26):6990-8. [Content Brief]
[4]. Provenzani R, et al., Scaffold hopping from (5-hydroxymethyl) isophthalates to multisubstituted pyrimidines diminishes binding affinity to the C1 domain of protein kinase C. PLoS One. 2018 Apr 11;13(4):e0195668. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
3-Heptanol-d4 Related Classifications
HY-134058S Related Classifications
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