Cyclopentanecarbonitrile is suitable for use as substrate to investigate the specific activity of nitrile- and amide- hydrolyzing enzymes isolated from Candida guilliermondii UFMG-Y65 cells， It is suitable for use as reagent to investigate the nitrile degradation by Candida guilliermondii CCT 7207 using free and immobilized cell systems.
| Pubchem Sid | 488185485 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488185485 |
| Sonrisas canónicas | C1CCC(C1)C#N |
| IUPAC Name | cyclopentanecarbonitrile |
| InChIKey | SVPZJHKVRMRREG-UHFFFAOYSA-N |
| INCHI | 1S/C6H9N/c7-5-6-3-1-2-4-6/h6H,1-4H2 |
| Isómeros SMILES | C1CCC(C1)C#N |
| WGK Alemania | 3 |
| Peso molecular | 95.14 |
| Beilstein | 1098717 |
| Reaxy-Rn | 1098717 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1098717&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic nitrogen compounds |
| Clase | Organonitrogen compounds |
| Subclass | Organic cyanides |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Nitriles |
| Alternative Parents | Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | Nitrile - Carbonitrile - Organopnictogen compound - Hydrocarbon derivative - Aliphatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as nitriles. These are compounds having the structure RC#N; thus C-substituted derivatives of hydrocyanic acid, HC#N. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 F2204243 | Certificate of Analysis | Mar 13, 2026 | C124215 |
| F2204309 | Certificate of Analysis | Mar 13, 2026 | C124215 |
| D2126130 | Certificate of Analysis | Feb 07, 2025 | C124215 |
| D2126131 | Certificate of Analysis | Feb 07, 2025 | C124215 |
| I2504862 | Certificate of Analysis | Jun 24, 2024 | C124215 |
| G2508299 | Certificate of Analysis | Jun 24, 2024 | C124215 |
| C2329092 | Certificate of Analysis | Mar 23, 2022 | C124215 |
| C2329129 | Certificate of Analysis | Mar 23, 2022 | C124215 |
| C2604177 | Certificate of Analysis | Mar 23, 2022 | C124215 |
| F2202232 | Certificate of Analysis | Mar 23, 2022 | C124215 |
| Solubilidad | Miscible with toluene. |
|---|---|
| Índice de refracción | n20/D 1.441 (lit.) |
| Punto de inflamación (°F) | 56°C(133°F) |
| Punto de inflamación (°C) | 56°C(133°F) |
| Punto de ebullición (°C) | 67-68°C/10mmHg |
| Punto de fusión (°C) | -76°C |
| Peso molecular | 95.140 g/mol |
| XLogP3 | 1.500 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 95.0735 Da |
| Monoisotopic Mass | 95.0735 Da |
| Topological Polar Surface Area | 23.800 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 92.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
