Cas no 261359-03-9 (Benzenemethanol, 4-methoxy-3-propoxy-)
Benzenemethanol, 4-methoxy-3-propoxy- Chemical and Physical Properties
Names and Identifiers
-
- Benzenemethanol, 4-methoxy-3-propoxy-
- MWLWMAJKJRTRCE-UHFFFAOYSA-N
- SCHEMBL6798353
- AKOS000247422
- 261359-03-9
- 3-(propyloxy)-4-methoxybenzyl alcohol
- DB-138663
- (4-Methoxy-3-propoxyphenyl)methanol
- 4-Methoxy-3-propoxybenzenemethanol
- SB84395
- 4-Methoxy-3-n-propoxybenzyl alcohol
-
- MDL: MFCD11149585
- Inchi: 1S/C11H16O3/c1-3-6-14-11-7-9(8-12)4-5-10(11)13-2/h4-5,7,12H,3,6,8H2,1-2H3
- InChI Key: MWLWMAJKJRTRCE-UHFFFAOYSA-N
- SMILES: O(CCC)C1C(=CC=C(CO)C=1)OC
Computed Properties
- Exact Mass: 345.12127
- Monoisotopic Mass: 196.109944368g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 14
- Rotatable Bond Count: 5
- Complexity: 150
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 1.8
- Topological Polar Surface Area: 38.7?2
Experimental Properties
- PSA: 87.9
Benzenemethanol, 4-methoxy-3-propoxy- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| abcr | AB427882-1 g |
4-Methoxy-3-n-propoxybenzyl alcohol |
261359-03-9 | 1g |
€482.30 | 2022-03-24 | ||
| abcr | AB427882-5 g |
4-Methoxy-3-n-propoxybenzyl alcohol |
261359-03-9 | 5g |
€1,123.50 | 2022-03-24 | ||
| Crysdot LLC | CD12090583-1g |
(4-Methoxy-3-propoxyphenyl)methanol |
261359-03-9 | 97% | 1g |
$437 | 2024-07-24 | |
| Crysdot LLC | CD12090583-5g |
(4-Methoxy-3-propoxyphenyl)methanol |
261359-03-9 | 97% | 5g |
$1177 | 2024-07-24 | |
| Ambeed | A505104-1g |
(4-Methoxy-3-propoxyphenyl)methanol |
261359-03-9 | 97% | 1g |
$441.0 | 2024-07-28 | |
| abcr | AB427882-1g |
4-Methoxy-3-n-propoxybenzyl alcohol; . |
261359-03-9 | 1g |
€1621.70 | 2024-08-03 | ||
| abcr | AB427882-5g |
4-Methoxy-3-n-propoxybenzyl alcohol |
261359-03-9 | 5g |
€1373.40 | 2023-09-04 |
Benzenemethanol, 4-methoxy-3-propoxy- Related Literature
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Yaqing Liu,Jiangtao Ren,Jing Li,Jiyang Liu,Erkang Wang Chem. Commun., 2012,48, 802-804
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Raktani Bikshapathi,Sai Prathima Parvathaneni,Vaidya Jayathirtha Rao Green Chem., 2017,19, 4446-4450
-
Li-Hua Gan,Rui Wu,Jian-Lei Tian,Patrick W. Fowler Phys. Chem. Chem. Phys., 2017,19, 419-425
Additional information on Benzenemethanol, 4-methoxy-3-propoxy-
Comprehensive Overview of Benzenemethanol, 4-methoxy-3-propoxy- (CAS No. 261359-03-9): Properties, Applications, and Industry Insights
Benzenemethanol, 4-methoxy-3-propoxy- (CAS No. 261359-03-9) is a specialized aromatic compound widely utilized in the pharmaceutical, fragrance, and specialty chemical industries. This methoxy-propoxy benzene derivative exhibits unique physicochemical properties, making it a valuable intermediate for synthesizing high-performance materials. With the growing demand for bioactive intermediates and green chemistry solutions, this compound has garnered significant attention due to its structural versatility and compatibility with sustainable synthesis protocols.
The molecular structure of Benzenemethanol, 4-methoxy-3-propoxy- combines a methoxy group at the 4-position and a propoxy group at the 3-position of the benzene ring, attached to a hydroxymethyl functional group. This configuration enhances its solubility in organic solvents while maintaining thermal stability—a critical feature for applications in high-temperature formulations. Recent studies highlight its role in photocatalysis and polymer stabilization, aligning with trends in energy-efficient chemical processes.
In the pharmaceutical sector, CAS 261359-03-9 serves as a precursor for drug discovery, particularly in developing central nervous system (CNS) therapeutics. Its ability to modulate lipophilicity and bioavailability makes it ideal for prodrug formulations. Industry reports indicate a surge in patents involving this compound for neuroprotective agents, coinciding with rising global interest in neurodegenerative disease research.
The fragrance industry leverages 4-methoxy-3-propoxy benzenemethanol for its odor-enhancing properties. Its balanced volatility and compatibility with essential oil blends cater to the demand for long-lasting perfumes and eco-friendly cosmetic ingredients. Market analysts correlate its adoption with the clean beauty movement, where consumers prioritize non-toxic scent carriers.
From an environmental perspective, Benzenemethanol, 4-methoxy-3-propoxy- demonstrates advantages in biodegradability testing compared to traditional aromatic alcohols. Regulatory bodies such as the EPA have flagged its potential for low-persistence formulations, addressing concerns about bioaccumulation. This aligns with the circular economy principles dominating chemical manufacturing discourse.
Technological advancements in catalytic hydrogenation have improved the cost-efficiency of producing CAS 261359-03-9 at scale. A 2023 study published in ACS Sustainable Chemistry & Engineering highlighted a novel enzyme-mediated synthesis route achieving 92% yield—a breakthrough for white biotechnology applications. Such innovations respond to the industry's push for carbon-neutral production methods.
Quality control protocols for 4-methoxy-3-propoxy benzenemethanol emphasize HPLC purity analysis and residual solvent monitoring, reflecting stringent ICH guidelines. Suppliers increasingly provide GC-MS certification to meet pharmaceutical-grade standards, a practice driven by supply chain transparency demands. These measures address frequent buyer queries regarding batch-to-batch consistency in online procurement platforms.
Emerging applications in flexible electronics have expanded the market potential for this compound. Its dielectric properties show promise in printed circuit board (PCB) coatings, particularly for wearable technology—a sector projected to grow at 14.5% CAGR through 2030. Material scientists are investigating its crosslinking behavior with epoxy resins for improved mechanical performance.
Storage and handling recommendations for Benzenemethanol, 4-methoxy-3-propoxy- specify nitrogen-blanketed containers to prevent oxidation, a common concern raised in chemical forum discussions. Technical datasheets advise maintaining temperatures below 25°C to preserve its hydrolytic stability, especially for international shipping scenarios. These precautions align with GHS-compliant labeling practices increasingly demanded by global distributors.
Market intelligence indicates that CAS 261359-03-9 prices fluctuate based on propylene oxide feedstock availability, a connection frequently searched in chemical commodity tracking platforms. The compound's regional production capacity shows concentration in Asia-Pacific facilities, reflecting broader shifts in fine chemical manufacturing geography. Traders monitor these patterns to optimize just-in-time inventory strategies.
Future research directions for 4-methoxy-3-propoxy benzenemethanol include exploring its ionic liquid derivatives for battery electrolyte systems—an area gaining traction due to electric vehicle market expansion. Preliminary data suggests its ether-functionalized structure could enhance lithium-ion transport, addressing key challenges in energy storage technology.
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