Cas no 24630-68-0 (DIISOPROPYL HYDROXYMETHYLPHOSPHONATE)
DIISOPROPYL HYDROXYMETHYLPHOSPHONATE Chemical and Physical Properties
Names and Identifiers
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- DIISOPROPYL HYDROXYMETHYLPHOSPHONATE
- di(propan-2-yloxy)phosphorylmethanol
- diisopropyl 1-hydroxymethylphosphonate
- hydroxymethyl phosphonic acid diisopropyl ester
- diisopropyl (hydroxymethyl)phosphonate
- DTXSID40446408
- AKOS000122758
- Phosphonic acid, P-(hydroxymethyl)-, bis(1-methylethyl) ester
- Phosphonic acid, (hydroxymethyl)-, bis(1-methylethyl) ester
- diisopropyl P-(hydroxymethyl)phosphonate
- diisopropyl P-(hydroxymethyl)-phosphonate
- bis(propan-2-yl) (hydroxymethyl)phosphonate
- SCHEMBL1378198
- (Hydroxymethyl) phosphonic acid, bis (1-methylethyl) ester
- (Hydroxymethyl)phosphonic acid, bis(1-methylethyl) ester
- UAXIBJPHBMEGSP-UHFFFAOYSA-N
- 24630-68-0
-
- MDL: MFCD00603008
- Inchi: 1S/C7H17O4P/c1-6(2)10-12(9,5-8)11-7(3)4/h6-8H,5H2,1-4H3
- InChI Key: UAXIBJPHBMEGSP-UHFFFAOYSA-N
- SMILES: P(CO)(=O)(OC(C)C)OC(C)C
Computed Properties
- Exact Mass: 196.08600
- Monoisotopic Mass: 196.08644602g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 12
- Rotatable Bond Count: 5
- Complexity: 153
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: 0.5
- Topological Polar Surface Area: 55.8?2
Experimental Properties
- PSA: 65.57000
- LogP: 1.97930
DIISOPROPYL HYDROXYMETHYLPHOSPHONATE Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Cooke Chemical | M8430655-250mg |
Diisopropyl(hydroxymethyl)phosphonate |
24630-68-0 | ≥95% | 250mg |
RMB 612.80 | 2025-02-21 | |
| Cooke Chemical | M8430655-1g |
Diisopropyl(hydroxymethyl)phosphonate |
24630-68-0 | ≥95% | 1g |
RMB 1830.40 | 2025-02-21 |
DIISOPROPYL HYDROXYMETHYLPHOSPHONATE Related Literature
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Joo Chuan Yeo,Kenry Lab Chip, 2016,16, 4082-4090
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Jason Y. C. Lim,Yong Yu,Guorui Jin,Kai Li,Yi Lu,Jianping Xie Nanoscale Adv., 2020,2, 3921-3932
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Thi Thu Tram Nguyen,Thanh Binh Nguyen Org. Biomol. Chem., 2021,19, 6015-6020
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4. Fatty acid eutectic mixtures and derivatives from non-edible animal fat as phase change materials?Pau Gallart-Sirvent,Marc Martín,Gemma Villorbina,Mercè Balcells,Aran Solé,Luisa F. Cabeza,Ramon Canela-Garayoa RSC Adv., 2017,7, 24133-24139
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Bin Han,Yasuo Shimizu,Gabriele Seguini,Celia Castro,Gérard Ben Assayag,Koji Inoue,Yasuyoshi Nagai,Sylvie Schamm-Chardon,Michele Perego RSC Adv., 2016,6, 3617-3622
Additional information on DIISOPROPYL HYDROXYMETHYLPHOSPHONATE
Comprehensive Guide to DIISOPROPYL HYDROXYMETHYLPHOSPHONATE (CAS No. 24630-68-0): Properties, Applications, and Market Insights
DIISOPROXYL HYDROXYMETHYLPHOSPHONATE (CAS 24630-68-0), often abbreviated as DIPHMP, is an organophosphorus compound with significant industrial and research applications. This comprehensive guide explores its chemical properties, synthesis methods, diverse applications, and emerging trends in the global market. As sustainability and green chemistry gain prominence, understanding specialized chemicals like DIPHMP becomes crucial for researchers and industry professionals.
The molecular structure of DIISOPROXYL HYDROXYMETHYLPHOSPHONATE features a central phosphorus atom bonded to hydroxylmethyl and isopropoxy groups. This unique configuration contributes to its water solubility and chelating properties, making it valuable in various formulations. With a molecular weight of 196.16 g/mol and typical appearance as a clear liquid, DIPHMP demonstrates excellent stability under normal storage conditions while maintaining reactivity for targeted applications.
In industrial applications, DIISOPROXYL HYDROXYMETHYLPHOSPHONATE serves as a key intermediate for flame retardant formulations, particularly in polymers and textiles. Recent studies highlight its potential as a green alternative to traditional halogenated flame retardants, addressing growing environmental concerns. The compound's ability to form stable complexes also makes it useful in water treatment systems for scale inhibition and corrosion control, especially in cooling towers and boiler systems.
The synthesis of DIPHMP typically involves the reaction of phosphorus trichloride with isopropyl alcohol, followed by hydroxymethylation. Manufacturers have developed optimized processes to achieve high purity levels (>98%) while minimizing byproducts. Quality control parameters for DIISOPROXYL HYDROXYMETHYLPHOSPHONATE include acid value, moisture content, and phosphorus content analysis, ensuring consistency for end-use applications.
Emerging research explores novel applications of CAS 24630-68-0 in biodegradable materials and renewable energy technologies. Scientists are investigating its potential as a ligand in catalyst systems for polymerization reactions and as an additive in electrolyte formulations for lithium-ion batteries. These developments align with global trends toward sustainable chemistry and circular economy principles.
From a market perspective, the demand for DIISOPROXYL HYDROXYMETHYLPHOSPHONATE shows steady growth, particularly in Asia-Pacific regions where flame retardant regulations are becoming stricter. Major manufacturers are investing in production capacity expansion and developing derivative products to meet diverse industry needs. Current price trends reflect raw material availability and energy costs, with typical commercial quantities available in drum and bulk container options.
Safety considerations for handling DIPHMP include standard laboratory precautions - proper ventilation, chemical-resistant gloves, and eye protection. While not classified as highly hazardous, material safety data sheets recommend avoiding prolonged skin contact and inhalation of vapors during processing. Storage in cool, dry areas away from strong oxidizers ensures long-term stability of the product.
Analytical methods for DIISOPROXYL HYDROXYMETHYLPHOSPHONATE characterization include HPLC, NMR spectroscopy, and titration techniques. These methods enable precise quantification in complex matrices and quality verification during production. Recent advancements in analytical instrumentation have improved detection limits and reduced analysis time for this compound.
Environmental fate studies indicate that CAS 24630-68-0 undergoes biodegradation under aerobic conditions, with half-life estimates varying based on environmental factors. Regulatory status varies by region, with most jurisdictions requiring standard chemical registration without special restrictions. Ongoing ecotoxicity studies contribute to the compound's environmental profile assessment.
Future prospects for DIPHMP include potential applications in electronic materials and advanced coatings. Research collaborations between academia and industry are exploring molecular modifications to enhance specific properties while maintaining favorable environmental characteristics. These innovations may open new market opportunities in high-tech sectors.
For researchers and procurement specialists seeking DIISOPROXYL HYDROXYMETHYLPHOSPHONATE, key selection criteria include purity grade, packaging options, and supplier technical support. Reputable suppliers provide comprehensive documentation including certificates of analysis, safety data sheets, and application guidance. Custom synthesis services are available for specialized derivatives or formulation requirements.
In conclusion, DIISOPROPYL HYDROXYMETHYLPHOSPHONATE (CAS 24630-68-0) represents a versatile organophosphorus compound with growing importance across multiple industries. Its balanced combination of chemical functionality and environmental profile positions it favorably in the evolving landscape of specialty chemicals. Continued research and development will likely uncover additional applications that leverage its unique molecular properties.
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