Cas no 76890-93-2 (Bis(4-hydroxybenzyl) Ether)
Bis(4-hydroxybenzyl) Ether Chemical and Physical Properties
Names and Identifiers
-
- Phenol, 4,4'-[oxybis(methylene)]bis-
- 4-[(4-hydroxyphenyl)methoxymethyl]phenol
- 4,4'-Dihydroxydibenzyl ether
- Bis(4-hydroxybenzyl) Ether
-
- Inchi: 1S/C14H14O3/c15-13-5-1-11(2-6-13)9-17-10-12-3-7-14(16)8-4-12/h1-8,15-16H,9-10H2
- InChI Key: OCOMKVVSXFCESC-UHFFFAOYSA-N
- SMILES: O(CC1C=CC(=CC=1)O)CC1C=CC(=CC=1)O
Computed Properties
- Exact Mass: 230.09400
Experimental Properties
- PSA: 49.69000
- LogP: 2.81460
Bis(4-hydroxybenzyl) Ether Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | H829010-100mg |
Bis(4-hydroxybenzyl) Ether |
76890-93-2 | 100mg |
$121.00 | 2023-05-18 | ||
| TRC | H829010-250mg |
Bis(4-hydroxybenzyl) Ether |
76890-93-2 | 250mg |
$259.00 | 2023-05-18 | ||
| TRC | H829010-500mg |
Bis(4-hydroxybenzyl) Ether |
76890-93-2 | 500mg |
$483.00 | 2023-05-18 | ||
| TRC | H829010-1000mg |
Bis(4-hydroxybenzyl) Ether |
76890-93-2 | 1g |
$ 795.00 | 2022-06-04 | ||
| TRC | H829010-1g |
Bis(4-hydroxybenzyl) Ether |
76890-93-2 | 1g |
$ 1200.00 | 2023-09-07 |
Bis(4-hydroxybenzyl) Ether Related Literature
-
Craig A. Kelly,David R. Rosseinsky Phys. Chem. Chem. Phys., 2001,3, 2086-2090
-
Denis V. Korchagin,Elena A. Yureva,Alexander V. Akimov,Eugenii Ya. Misochko,Gennady V. Shilov,Artem D. Talantsev,Roman B. Morgunov,Alexander A. Shakin,Sergey M. Aldoshin,Boris S. Tsukerblat Dalton Trans., 2017,46, 7540-7548
-
A. B. F. da Silva,K. Capelle Phys. Chem. Chem. Phys., 2009,11, 4564-4569
-
Guiying Zhang,Maosheng Cheng,Yanni Li,Keliang Liu,Lifeng Cai Chem. Commun., 2013,49, 11086-11088
Additional information on Bis(4-hydroxybenzyl) Ether
Comprehensive Overview of Bis(4-hydroxybenzyl) Ether (CAS No. 76890-93-2): Properties, Applications, and Industry Insights
Bis(4-hydroxybenzyl) Ether (CAS No. 76890-93-2), also known as 4,4'-Dihydroxydiphenylmethane dimethyl ether, is a phenolic compound with significant industrial and research relevance. This aromatic ether is characterized by its two hydroxyl-functionalized benzyl groups linked by an ether bridge. Its molecular structure (C14H14O3) grants it unique physicochemical properties, including thermal stability and solubility in polar organic solvents, making it valuable for specialized applications.
In recent years, the demand for high-purity phenolic derivatives like Bis(4-hydroxybenzyl) Ether has surged due to their role in polymer synthesis and pharmaceutical intermediates. Researchers frequently search for "Bis(4-hydroxybenzyl) Ether solubility" or "CAS 76890-93-2 synthesis method," reflecting its technical importance. The compound’s ability to act as a crosslinking agent in epoxy resins aligns with the growing interest in sustainable materials and bio-based polymers, a trending topic in green chemistry.
From a safety and handling perspective, Bis(4-hydroxybenzyl) Ether requires standard laboratory precautions. While not classified as hazardous under major regulatory frameworks, proper storage away from strong oxidizers is recommended. Its melting point (160–165°C) and molecular weight (230.26 g/mol) are frequently cited in technical datasheets, addressing common queries like "Bis(4-hydroxybenzyl) Ether physical properties."
The compound’s applications extend to advanced material science, where it serves as a precursor for flame-retardant additives and liquid crystal displays (LCDs). Industry reports highlight its niche use in electronic encapsulation, correlating with the rise in "high-performance polymer additives" searches. Additionally, its potential in antioxidant formulations has sparked academic interest, particularly in studies exploring "phenolic antioxidants in plastics."
Analytical methods for Bis(4-hydroxybenzyl) Ether typically involve HPLC or GC-MS, with purity grades (>98%) being critical for research applications. Manufacturers emphasize batch-to-batch consistency, responding to concerns about "CAS 76890-93-2 supplier reliability." The compound’s UV absorption properties also make it relevant in photostability studies, a subtopic gaining traction in material degradation research.
Emerging trends link Bis(4-hydroxybenzyl) Ether to circular economy initiatives, as its derivatives show promise in recyclable thermosets. This aligns with frequent searches for "eco-friendly chemical alternatives." Furthermore, its role in drug delivery systems—particularly in biodegradable carriers—has been explored in recent patents, addressing the "pharmaceutical excipient innovation" niche.
In summary, Bis(4-hydroxybenzyl) Ether (CAS No. 76890-93-2) exemplifies how specialized chemicals bridge traditional and cutting-edge industries. Its versatility across material science, green chemistry, and life sciences ensures continued relevance, while evolving applications respond to global demands for sustainable innovation.
76890-93-2 (Bis(4-hydroxybenzyl) Ether) Related Products
- 57726-26-8(4-(Ethoxymethyl)phenol)
- 5355-17-9(4-(Methoxymethyl)phenol)
- 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
- 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
- 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
- 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
- 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
- 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
- 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
- 89640-58-4(2-Iodo-4-nitrophenylhydrazine)