3-Heptanol
Based on 1 Customer Validation
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.
- CAS No.: 589-82-2
- Formula: C7H16O
- Molecular Weight:116.20
-
Storage:
Store at room temperature 3 years.
In solvent -80°C, 2 years , -20°C, 1 year
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
-
Biological Activity
-
Chemical Information
- Purity & Documentation
- References
-
Help & FAQs
Biological Activity
Chemical Information
-
CAS No. 589-82-2
-
Appearance Liquid
-
Molecular Weight 116.20
-
Formula C7H16O
-
Color Colorless to light yellow
-
SMILES
OC(CC)CCCC
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
Store at room temperature 3 years
In solvent -80°C 2 years -20°C 1 year
Purity & Documentation
-
Data Sheet (264 KB)
-
SDS (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
-
Handling Instructions (2659 KB)
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 Related Classifications
HY-134058 Related Classifications
Powered by Bioz