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Trixylenyl phosphate
[CAS# 25155-23-1]

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Complete supplier list of Trixylenyl phosphate
Identification
Classification Organic raw materials >> Inorganic acid ester
Name Trixylenyl phosphate
Synonyms Dimethylphenol 1,1',1''-phosphate; Xylenol phosphate; Antiblaze 524; Antiblaze TXP; Coalite NTP; Durad 220X; Phosflex 179; Phosphoric acid trixylyl ester; TXP; Trixylyl phosphate
Molecular Structure CAS # 25155-23-1, Trixylenyl phosphate, Dimethylphenol 1,1',1''-phosphate, Xylenol phosphate, Antiblaze 524, Antiblaze TXP, Coalite NTP, Durad 220X, Phosflex 179, Phosphoric acid trixylyl ester, TXP, Trixylyl phosphate
Molecular Formula C24H27O4P
Molecular Weight 410.45
CAS Registry Number 25155-23-1
EC Number 246-677-8
SMILES CC1=CC(=CC(=C1)OP(=O)(OC2=CC(=CC(=C2)C)C)OC3=CC(=CC(=C3)C)C)C
Properties
Density 1.2±0.1 g/cm3, Calc.*, 1.55 g/mL
Index of Refraction 1.570, Calc.*
Boiling Point 490.8±45.0 ºC (760 mmHg), Calc.*
Flash Point 263.8±49.1 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol   GHS08 Danger    Details
Hazard Statements H315-H317-H319-H335-H360-H360F    Details
Precautionary Statements P261-P280-P305+P351+P338-P308+P313    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute hazardous to the aquatic environmentAquatic Acute1H400
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Reproductive toxicityRepr.1BH360
Specific target organ toxicity - repeated exposureSTOT RE2H373
Eye irritationEye Irrit.2H319
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Reproductive toxicityRepr.2H361
Skin sensitizationSkin Sens.1H317
Reproductive toxicityRepr.1BH360F
SDS Available
up Discovory and Applicatios
Trixylenyl phosphate, also known as tri-ortho-cresyl phosphate (TOCP), is an organophosphate compound that has drawn significant attention due to its unique chemical properties and diverse applications across various industries. The discovery of trixylenyl phosphate dates back to the early 20th century, with initial investigations into the properties and potential applications of phosphate esters.

Trixylenyl phosphate is formed by the esterification of phosphoric acid with a mixture of ortho-cresol isomers, leading to a compound that exhibits excellent solvating properties. This chemical structure contributes to its effectiveness as a plasticizer, flame retardant, and lubricant. One of the distinguishing features of trixylenyl phosphate is its ability to dissolve a wide range of polymers, enhancing their mechanical properties and processing characteristics.

In industrial applications, trixylenyl phosphate is widely used as a plasticizer in the production of flexible polyvinyl chloride (PVC) products. Its high compatibility with PVC enhances the material's flexibility, durability, and resistance to heat and chemicals. This makes it particularly valuable in the manufacturing of electrical cables, flooring, and synthetic leather, where flexibility and stability are essential.

Another important application of trixylenyl phosphate is its role as a flame retardant. When incorporated into polymers, it imparts fire-resistant properties, reducing the flammability of materials and enhancing their safety in various applications, including construction materials and consumer goods. The effectiveness of trixylenyl phosphate in this regard has led to its use in numerous industries, including automotive, aerospace, and electronics.

Moreover, trixylenyl phosphate has found applications in the formulation of lubricants and hydraulic fluids. Its excellent thermal stability and low volatility make it suitable for high-temperature applications, ensuring reliable performance in challenging environments. Additionally, its lubricating properties help reduce friction and wear in mechanical systems, contributing to improved efficiency and longevity.

Despite its widespread use, concerns regarding the potential health and environmental impacts of trixylenyl phosphate have emerged. Research has indicated that exposure to organophosphate compounds may pose risks, including neurotoxic effects. Consequently, regulatory bodies have begun to evaluate the safety of trixylenyl phosphate and other similar compounds, prompting the exploration of alternative materials in some applications.

As research continues to expand our understanding of trixylenyl phosphate, efforts are underway to develop safer alternatives that can replace it in applications where potential risks are a concern. Innovations in materials science and chemistry are likely to yield new compounds with similar or enhanced properties, ensuring that industry needs are met while prioritizing safety and environmental sustainability.

The ongoing study of trixylenyl phosphate and its derivatives highlights the need for a balanced approach to utilizing this versatile chemical while addressing health and environmental concerns associated with its use.
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