≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Sorrisi canonici | C#CCCCCCCC#C |
|---|---|
| IUPAC Name | deca-1,9-diyne |
| InChIKey | ILVDYAGPHFWNQI-UHFFFAOYSA-N |
| INCHI | 1S/C10H14/c1-3-5-7-9-10-8-6-4-2/h1-2H,5-10H2 |
| Isomeri SMILES | C#CCCCCCCC#C |
| Numero UN | UN3295 |
| Gruppo di imballaggio | III |
| Peso molecolare | 134.22 |
| Reaxy-Rn | 1734594 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1734594&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 | Acetylides |
| Classe | Not available |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Acetylides |
| Alternative Parents | Unsaturated aliphatic hydrocarbons Acyclic acetylenes |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Acetylide - Unsaturated aliphatic hydrocarbon - Unsaturated hydrocarbon - Acyclic acetylene - Acetylene - Hydrocarbon - Aliphatic acyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as acetylides. These are compounds arising by replacement of one or both hydrogen atoms of acetylene (ethyne) by a metal or other cationic group. E.g. NaC#CH monosodium acetylide. By extension, analogous compounds derived from terminal acetylenes, RC#CH. The class is limited here to derivatives of acetylene where the hydrogen atom is replaced with an element with similar or lower electronegativity that carbon. |
| External Descriptors | terminal acetylenic compound - alkadiyne |
| Indice di rifrazione | 1.451 |
|---|---|
| Punto di infiammabilità (°F) | 60 ℃ |
| Punto di infiammabilità (°C) | 60 ℃ |
| Punto di ebollizione (°C) | 72°C |
| Peso molecolare | 134.220 g/mol |
| XLogP3 | 3.500 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 5 |
| Exact Mass | 134.11 Da |
| Monoisotopic Mass | 134.11 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 127.000 |
| 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 |
| 1. Qianchun Zhang, Xiaolan Zhang, Bingnian Yang, Shan Liu, Ming Wen, Linchun Bao, Li Jiang. (2021) Development of a highly efficient in-tube solid-phase microextraction system coupled with UHPLC-MS/MS for analyzing trace hydroxyl polycyclic aromatic hydrocarbons in biological samples. JOURNAL OF SEPARATION SCIENCE, 45 (4): (919-928). [PMID:34923746] [10.1002/jssc.202100751] |
G2610509