≥99.5 atom% D for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature,Argon charged Ships Normal 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.
2-Propanol-d 8 (Isopropanol-d 8 ) is a deuterated derivative of isopropanol. Generation and decay of correlated radical pairs (SCRP) during the reduction of acetone(D 6 ) in 2-propanol(D 8 ) have been studied by Fourier transform-electron paramagnetic resonance (FT-EPR) spectroscopy. It participates as solvent during the evaluation of triplet decay constants, triplet lifetime and photoreduction rate constants of benzophenone.
Application
2-Propanol-d 8 may be used in the preparation of 2-iodopropane-d 7 .
| カノニカル・スマイル | CC(C)O |
|---|---|
| IUPAC Name | 1,1,1,2,3,3,3-heptadeuterio-2-deuteriooxypropane |
| InChIKey | KFZMGEQAYNKOFK-PIODKIDGSA-N |
| INCHI | 1S/C3H8O/c1-3(2)4/h3-4H,1-2H3/i1D3,2D3,3D,4D |
| 異性体SMILES | [2H]C([2H])([2H])C([2H])(C([2H])([2H])[2H])O[2H] |
| WGKドイツ | 3 |
| 分子量 | 68.14 |
| Beilstein | 1816231 |
| Reaxy-Rn | 635639 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=635639&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 oxygen compounds |
| 分類 | Organooxygen compounds |
| Subclass | Alcohols and polyols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Secondary alcohols |
| Alternative Parents | Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Secondary alcohol - Hydrocarbon derivative - Aliphatic acyclic compound |
| 説明 | This compound belongs to the class of organic compounds known as secondary alcohols. These are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R') (R,R'=alkyl, aryl). |
| External Descriptors | Not available |
| 感度 | heat sensitive |
|---|---|
| 屈折率 | 1.3728 |
| 引火点（°F） | 53.6 °F |
| 引火点（°C） | 12 °C |
| 沸点（°C） | 82°C |
| 融点（°C） | -89.5°C |
| 分子量 | 68.140 g/mol |
| XLogP3 | 0.300 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 68.1077 Da |
| Monoisotopic Mass | 68.1077 Da |
| Topological Polar Surface Area | 20.200 Ų |
| Heavy Atom Count | 4 |
| Formal Charge | 0 |
| Complexity | 10.800 |
| Isotope Atom Count | 8 |
| 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. Wang Tianjiao, Xin Yu, Chen Bingfeng, Zhang Bin, Luan Sen, Dong Minghua, Wu Yuxuan, Cheng Xiaomeng, Liu Ye, Liu Huizhen, Han Buxing. (2024) Selective hydrodeoxygenation of α, β-unsaturated carbonyl compounds to alkenes. Nature Communications, 15 (1): (1-10). [PMID:38461211] [10.1038/s41467-024-46383-9] |
