≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature 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.
Dibutyl butylphosphonate is a plasticizer used in nickel(II)-selective sensors with a dibenzocyclam-nickel ionophore PVC membrane.
| Pubchem Sid | 488180090 |
|---|---|
| Sonrisas canónicas | CCCCOP(=O)(CCCC)OCCCC |
| IUPAC Name | 1-[butoxy(butyl)phosphoryl]oxybutane |
| InChIKey | JPGXOMADPRULAC-UHFFFAOYSA-N |
| INCHI | 1S/C12H27O3P/c1-4-7-10-14-16(13,12-9-6-3)15-11-8-5-2/h4-12H2,1-3H3 |
| Isómeros SMILES | CCCCOP(=O)(CCCC)OCCCC |
| WGK Alemania | 3 |
| RTECS | SZ7000000 |
| Peso molecular | 250.31 |
| Beilstein | 1777999 |
| Reaxy-Rn | 1777999 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1777999&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 acids and derivatives |
| Clase | Organic phosphonic acids and derivatives |
| Subclass | Phosphonic acid diesters |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Dialkyl alkylphosphonates |
| Alternative Parents | Phosphonic acid esters Organopnictogen compounds Organophosphorus compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Dialkyl alkylphosphonate - Phosphonic acid ester - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organophosphorus compound - Organooxygen compound - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as dialkyl alkylphosphonates. These are compounds containing a phosphonic acid that is diesterified with alkyl groups, and the phosphorus atom is also directly attached to an alkyl group. |
| External Descriptors | Not available |
| Índice de refracción | n20D1.43 (lit.) |
|---|---|
| Punto de inflamación (°F) | 235.4 °F |
| Punto de inflamación (°C) | 113 °C |
| Punto de ebullición (°C) | 283° C (lit.) |
| Peso molecular | 250.310 g/mol |
| XLogP3 | 3.200 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 11 |
| Exact Mass | 250.17 Da |
| Monoisotopic Mass | 250.17 Da |
| Topological Polar Surface Area | 35.500 Ų |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 181.000 |
| 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. Jingjing Xiao, Li Li, Zhengwen Li, Mengjia Hu, Sisi Liu, Jia Tu, Baining Lin, Hongqing Wang, Zhihong Xiao, Rukuan Liu, Xiaoyu Cao. (2025) Dialkyl-(2-amino-2-(hydroxyimino) ethyl) phosphonate as a new uranium extractant: Extraction mechanism and cost analysis. Results in Engineering, [PMID:] [10.1016/j.rineng.2025.108120] |
K2204458