CAS 95906-11-9

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

Description:

Tris(2,4-di-tert-butylphenyl) phosphate, with the CAS number 95906-11-9, is an organophosphate compound primarily used as a flame retardant and plasticizer in various applications, including polymers and coatings. This substance is characterized by its high thermal stability and resistance to degradation, making it suitable for use in high-temperature environments. It features a phosphate group bonded to three bulky 2,4-di-tert-butylphenyl groups, which contribute to its effectiveness as a flame retardant by interrupting the combustion process. The bulky tert-butyl groups enhance its hydrophobicity and reduce volatility, which helps in maintaining its performance in formulations. Additionally, Tris(2,4-di-tert-butylphenyl) phosphate exhibits low toxicity and is considered to have a favorable environmental profile compared to other flame retardants. However, like many organophosphates, it should be handled with care to avoid potential health risks associated with exposure. Its applications extend beyond flame retardancy, including use in lubricants and as an additive in various industrial processes.

Formula: 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

InChI key: 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

Synonyms:

• 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

Formula: C₄₂H₆₃O₄P

Color and Shape: White Solid

Molecular weight: 662.4464

Ref: 45-1800184

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

CAS: 95906-11-9

Formula: C₄₂H₆₃O₄P

Purity: 98%

Color and Shape: Solid

Molecular weight: 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.

Formula: C₄₂H₆₃O₄P

Purity: 99.73%

Color and Shape: Solid

Molecular weight: 662.92

Ref: TM-T13206

Tris (2,4-ditert-butylphenyl) Phosphate

CAS: 95906-11-9

Formula: C₄₂H₆₃O₄P

Color and Shape: Pale Yellow Solid

Molecular weight: 662.94

Ref: 4Z-P-135006

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

CAS: 95906-11-9

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

Purity: 99%

Molecular weight: 662.92g/mol

Ref: 54-OR1025517

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

CAS: 95906-11-9

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

Purity: ≥98%

Molecular weight: 662.92g/mol

Ref: 54-BUP11387

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

CAS: 95906-11-9

Formula: C₄₂H₆₃O₄P

Color and Shape: Neat

Molecular weight: 662.92

Ref: 04-C17894345

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

CAS: 95906-11-9

Color and Shape: 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);

Formula: C₄₂H₆₃O₄P

Color and Shape: Light Yellow

Molecular weight: 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

Formula: C₄₂H₆₃O₄P

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 662.92 g/mol

Ref: 3D-VDA90611