118-82-1 | 4,4'-Methylenebis(2,6-di-tert-butylphenol)

Packsize	Purity	Availability	Price	Discounted Price
25g	98%	in stock	$15.00	$11.00
50g	98%	in stock	$24.00	$17.00
100g	98%	in stock	$30.00	$21.00
500g	98%	in stock	$122.00	$85.00

Description

• Catalog Number: AB66289
• Chemical Name: 4,4'-Methylenebis(2,6-di-tert-butylphenol)
• CAS Number: 118-82-1
• Molecular Formula: C29H44O2
• Molecular Weight: 424.6585
• MDL Number: MFCD00008822
• SMILES: CC(c1cc(Cc2cc(c(c(c2)C(C)(C)C)O)C(C)(C)C)cc(c1O)C(C)(C)C)(C)C
• NSC Number: 30551

Computed Properties

• Complexity: 480
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 31
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 6
• XLogP3: 9.8

Upstream Synthesis Route

4,4'-Methylenebis(2,6-di-tert-butylphenol) is a versatile chemical compound widely used in chemical synthesis for its antioxidant properties. In the field of synthetic chemistry, this compound plays a crucial role as a stabilizer and inhibitor, particularly in the production of polymers, plastics, and various industrial materials. Its ability to scavenge free radicals and prevent oxidation makes it an essential additive in the formulation of these materials, helping to prolong their lifespan and maintain their structural integrity. Additionally, 4,4'-Methylenebis(2,6-di-tert-butylphenol) is utilized in the synthesis of specialty chemicals and pharmaceuticals where protection against degradation due to oxidative processes is needed. Its effectiveness as an antioxidant makes it a valuable tool in the arsenal of chemists working on developing advanced materials and products with enhanced durability and stability.

Literature

• Natural and synthetic antioxidant additives for improving the performance of new biolubricant formulations.

  Journal of agricultural and food chemistry 20111228

• Discovery of novel SERCA inhibitors by virtual screening of a large compound library.

  European journal of medicinal chemistry 20110501

• Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.

  Journal of molecular graphics & modelling 20061101

• Antioxidant activity of o-bisphenols: the role of intramolecular hydrogen bonding.

  The Journal of organic chemistry 20030627

• Structure-activity relationships for a large diverse set of natural, synthetic, and environmental estrogens.

  Chemical research in toxicology 20010301