CAS 95906-11-9

Tris(2,4-di-terc-butilfenil) fosfato

Descripción:

Tris(2,4-di-terc-butilfenil) fosfato, con el número CAS 95906-11-9, es un compuesto organofosforado utilizado principalmente como retardante de llama y plastificante en diversas aplicaciones, incluyendo polímeros y recubrimientos. Esta sustancia se caracteriza por su alta estabilidad térmica y resistencia a la degradación, lo que la hace adecuada para su uso en entornos de alta temperatura. Presenta un grupo fosfato unido a tres voluminosos grupos 2,4-di-terc-butilfenilo, que contribuyen a su efectividad como retardante de llama al interrumpir el proceso de combustión. Los voluminosos grupos terc-butilo mejoran su hidrofobicidad y reducen la volatilidad, lo que ayuda a mantener su rendimiento en formulaciones. Además, Tris(2,4-di-terc-butilfenil) fosfato exhibe baja toxicidad y se considera que tiene un perfil ambiental favorable en comparación con otros retardantes de llama. Sin embargo, al igual que muchos organofosforados, debe manejarse con cuidado para evitar riesgos potenciales para la salud asociados con la exposición. Sus aplicaciones se extienden más allá de la resistencia a la llama, incluyendo su uso en lubricantes y como aditivo en varios procesos industriales.

Fórmula: C₄₂H₆₃O₄P

InChI: InChI=1S/C42H63O4P/c1-37(2,3)28-19-22-34(31(25-28)40(10,11)12)44-47(43,45-35-23-20-29(38(4,5)6)26-32(35)41(13,14)15)46-36-24-21-30(39(7,8)9)27-33(36)42(16,17)18/h19-27H,1-18H3

Clave InChI: InChIKey=AZSKHRTUXHLAHS-UHFFFAOYSA-N

SMILES: P(OC1=C(C(C)(C)C)C=C(C(C)(C)C)C=C1)(OC2=C(C(C)(C)C)C=C(C(C)(C)C)C=C2)(OC3=C(C(C)(C)C)C=C(C(C)(C)C)C=C3)=O

Sinónimos:

• D 16-834
• Phenol, 2,4-bis(1,1-dimethylethyl)-, 1,1′,1′′-phosphate
• P 3
• Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphate (3:1)
• Tris(2,4-di-tert-butylphenyl) phosphate

Tris(2,4-di-tert-butylphenyl)phosphate (Tri(2,4-di-tert-butylphenyl) phosphate)

CAS: 95906-11-9

Other aromatic phosphoric esters and their salts, including lactophosphates; their halogenated, sulfonated, nitrated or nitrosated derivatives

Fórmula: C₄₂H₆₃O₄P

Forma y color: White Solid

Peso molecular: 662.4464

Ref: 45-1800184

Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphate (3:1)

CAS: 95906-11-9

Fórmula: C₄₂H₆₃O₄P

Pureza: 98%

Forma y color: Solid

Peso molecular: 662.9210

Ref: IN-DA01CCOU

Tris(2,4-di-tert-butylphenyl)phosphate

CAS: 95906-11-9

Tris(2,4-di-tert-butylphenyl)phosphate (TDTBPP) inhibits secretory phospholipase A2 (sPLA2) with anti-inflammatory effect. Cost-effective and quality-assured.

Fórmula: C₄₂H₆₃O₄P

Pureza: 99.73%

Forma y color: Solid

Peso molecular: 662.92

Ref: TM-T13206

Tris (2,4-ditert-butylphenyl) Phosphate

CAS: 95906-11-9

Fórmula: C₄₂H₆₃O₄P

Forma y color: Pale Yellow Solid

Peso molecular: 662.94

Ref: 4Z-P-135006

Tris(2,4-Di-Tert-Butylphenyl) Phosphate

CAS: 95906-11-9

Tris(2,4-Di-Tert-Butylphenyl) Phosphate

Pureza: 99%

Peso molecular: 662.92g/mol

Ref: 54-OR1025517

Tris(2,4-di-tert-butylphenyl)phosphate

CAS: 95906-11-9

Tris(2,4-di-tert-butylphenyl)phosphate

Pureza: ≥98%

Peso molecular: 662.92g/mol

Ref: 54-BUP11387

Tris(2,4-di-tert-butylphenyl) phosphate

CAS: 95906-11-9

Fórmula: C₄₂H₆₃O₄P

Forma y color: Neat

Peso molecular: 662.92

Ref: 04-C17894345

Tris(2,4-di-tert-butylphenyl)phosphate

CAS: 95906-11-9

Forma y color: Light Yellow

Ref: 86-MM3963.10

Tris(2,4-di-tert-butylphenyl)phosphate

CAS: 95906-11-9

Stability Moisture Sensitive
Applications Tris(2,4-di-tert-butylphenyl)phosphate is used as a processing stabilizer for polymers.
References Thilen, M., et al.: J. Appl. Polym. Sci., 76, 938 (2000); Pfaendner, R., et al.: Polym. Degrad. Stab., 91, 2249 (2006);

Fórmula: C₄₂H₆₃O₄P

Forma y color: Light Yellow

Peso molecular: 662.92

Ref: TR-T884500

Tris(2,4-di-tert-butylphenyl)phosphate

CAS: 95906-11-9

Tris(2,4-di-tert-butylphenyl)phosphate (TDBP) is a phosphite that is used as an antioxidant. TDBP has been shown to inhibit the formation of secretory phospholipase A2 (sPLA2), which in turn inhibits the release of arachidonic acid and prostaglandin E2. TDBP also inhibits the activity of hydrogen bond polymerase chain reaction (PCR). This inhibition has been shown to be due to its ability to bind to DNA and prevent the synthesis of RNA, which decreases the production of proteins necessary for cell division. The matrix effect can be used in analytical methods because it has a high solubility in organic solvents and is stable at alkaline pH. TDBP can be used as a sample preparation reagent for mitochondrial membrane potential measurements because it increases mitochondrial membrane potential by inhibiting calcium ion influx. It also exhibits chemical properties such as being a strong base, forming

Fórmula: C₄₂H₆₃O₄P

Pureza: Min. 95%

Forma y color: Powder

Peso molecular: 662.92 g/mol

Ref: 3D-VDA90611