CAS 14802-03-0

2-Ethylhexyl (2-ethylhexyl)phosphonate

Description:

2-Ethylhexyl (2-ethylhexyl)phosphonate, with the CAS number 14802-03-0, is an organophosphorus compound characterized by its phosphonate functional group. It typically appears as a colorless to pale yellow liquid and is known for its low volatility and moderate solubility in organic solvents. This compound exhibits properties such as being a good plasticizer and is often utilized in the formulation of various materials, including plastics and coatings. Its chemical structure includes a phosphonate group attached to a branched alkyl chain, which contributes to its hydrophobic characteristics. Additionally, 2-ethylhexyl phosphonates are recognized for their potential applications in the extraction of metal ions and as flame retardants. Safety data indicates that, like many organophosphorus compounds, it should be handled with care due to potential toxicity and environmental concerns. Overall, 2-ethylhexyl (2-ethylhexyl)phosphonate is valued in industrial applications for its functional properties while necessitating appropriate safety measures during use.

Formula: C₁₆H₃₅O₃P

InChI: InChI=1S/C16H35O3P/c1-5-9-11-15(7-3)13-19-20(17,18)14-16(8-4)12-10-6-2/h15-16H,5-14H2,1-4H3,(H,17,18)

InChI key: InChIKey=ZDFBXXSHBTVQMB-UHFFFAOYSA-N

SMILES: C(CP(OCC(CCCC)CC)(=O)O)(CCCC)CC

Synonyms:

• (2-Ethylhexyl)phosphonic acid, mono(2-ethylhexyl) ester
• (2-Ethylhexyl)phosphonic acidmono(2-ethylhexyl) ester
• 1-Hexanol,2-ethyl-, (2-ethylhexyl)phosphonate
• 2-Ethylhexyl (2-ethylhexyl)phosphonate
• 2-Ethylhexyl 2-Ethyl Hexyphosphonic Acid
• 2-Ethylhexyl 2-ethylhexyphosphonate
• 2-Ethylhexyl Hydrogen (2-Ethylhexyl)Phosphonate
• 2-Ethylhexyl hydrogen-2-ethylhexylphosphonate
• 2-Ethylhexylhydrogen (2-ethylhexyl)phosphonate
• 2-Ethylhexylhydrogen-2-ethylhexylphosphonat
• Hehehp
• Hidrogeno-2-Etilhexilfosfonato De 2-Etilhexilo
• Hydrogeno-2-ethylhexylphosphonate de 2-ethylhexyle
• Ksm 17
• Mono(2-ethylhexyl)2-ethylhexylphosphonate
• Moop
• P 507
• Pc 88A
• Pc88A
• Phosphonic Acid, 2-Ethylhexyl-, Mono-2-Ethylhexyl
• Phosphonic acid, (2-ethylhexyl)-, mono(2-ethylhexyl) ester
• Phosphonic acid, P-(2-ethylhexyl)-, mono(2-ethylhexyl) ester

Phosphonic acid, P-(2-ethylhexyl)-, mono(2-ethylhexyl) ester

CAS: 14802-03-0

Formula: C₁₆H₃₅O₃P

Purity: 98%

Color and Shape: Liquid

Molecular weight: 306.4211

Ref: IN-DA001FDS

2-Ethylhexylhydrogen-2-Ethylhexylphosphonate

CAS: 14802-03-0

2-Ethylhexylhydrogen-2-Ethylhexylphosphonate

Purity: 95%

Molecular weight: 306.42g/mol

Ref: 54-OR1030945

Mono-2-ethylhexyl (2-Ethylhexyl)phosphonate

CAS: 14802-03-0

Formula: C₁₆H₃₅O₃P

Purity: >95.0%(qNMR)

Color and Shape: Colorless to Light yellow clear liquid

Molecular weight: 306.43

Ref: 3B-M2871

2-Ethylhexylphosphonic acid mono-2-ethylhexyl ester

CAS: 14802-03-0

Sodium carbonate is a chemical compound that is used as an alkaline substance in the laboratory. It is also used in the manufacture of detergents, glass, and textiles. Sodium carbonate has been shown to be an extractant for 2-ethylhexylphosphonic acid mono-2-ethylhexyl ester. It has been shown to react with acidic sodium salts to form a copper complex and adsorb onto the surface of hydrochloric acid at high concentrations. The Langmuir adsorption isotherm shows that 2-ethylhexylphosphonic acid mono-2-ethylhexyl ester has an optimum concentration at around 3 milliliters per gram, with a kinetic data of 4.74 x 10^4 mL/g/sec. The kinetic data also indicates that this reaction proceeds via a Langmuir adsorption mechanism.

Formula: C₁₆H₃₅O₃P

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 306.42 g/mol

Ref: 3D-FE30162