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1-Phenyl-1,2-Ethanediol

    • Product Name 1-Phenyl-1,2-Ethanediol
    • Alias Phenyl Ethylene Glycol
    • Einecs 202-846-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    771441

    Chemical Name 1-Phenyl-1,2-Ethanediol
    Cas Number 93-56-1
    Molecular Formula C8H10O2
    Molar Mass 138.17 g/mol
    Appearance White to off-white solid
    Melting Point 54-58°C
    Boiling Point 145-147°C at 15 mmHg
    Density 1.161 g/cm³
    Solubility In Water Slightly soluble
    Refractive Index 1.553
    Smiles C1=CC=C(C=C1)C(CO)O
    Inchi InChI=1S/C8H10O2/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8-10H,6H2
    Synonyms Phenylethylene glycol, α-Phenylethylene glycol
    Storage Temperature Store at 2-8°C

    As an accredited 1-Phenyl-1,2-Ethanediol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, screw cap, white label displaying "1-Phenyl-1,2-Ethanediol, 99%, 100g," hazard pictograms, supplier details.
    Shipping **Shipping Description for 1-Phenyl-1,2-Ethanediol:** Ship in tightly sealed containers, protected from light, heat, and moisture. Store and transport at room temperature. Ensure compliance with local, national, and international chemical transport regulations. Provide appropriate hazard labeling and safety data sheets. Avoid contact with incompatible substances and handle with standard personal protective equipment.
    Storage 1-Phenyl-1,2-ethanediol should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers and acids. Protect from moisture and direct sunlight. Store at room temperature and avoid prolonged exposure to air to minimize degradation. Proper labeling and handling according to safety guidelines are recommended.
    Application of 1-Phenyl-1,2-Ethanediol

    Applications of 1-Phenyl-1,2-Ethanediol in Industrial Manufacturing

    As a core manufacturer of 1-Phenyl-1,2-Ethanediol, we supply this specialized intermediate to a focused range of high-value sectors. Our material enables precision synthesis and strict compliance in these industries, offering both high purity and reliable supply security for advanced downstream formulations.

    1. Chiral Pharmaceutical Intermediate Synthesis

    1-Phenyl-1,2-Ethanediol acts as a critical chiral building block in the preparation of various enantiomerically pure active pharmaceutical ingredients (APIs), especially in antihypertensive and antifungal drug manufacturing. Its stereochemical integrity determines the biological activity and safety profile of the final API. Downstream pharmaceutical production integrates our material during the key enantioselective transformation and resolution steps, with the final purified product meeting regulatory standards for regulated medicinal compounds.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • EU Good Manufacturing Practice Directive 2003/94/EC
    • United States Pharmacopoeia (USP), European Pharmacopoeia (Ph. Eur.), Japanese Pharmacopoeia (JP)
    • FDA 21 CFR 210/211 (Finished Pharmaceuticals)

    Typical usage ratio

    • 0.5–3 molar equivalents relative to target chiral center; actual ratio depends on specific synthetic route and reaction optimization studies

    Downstream process integration

    • Enter synthesis during asymmetric dihydroxylation, chiral resolution, or Grignard coupling stages; removed or transformed in later purification or derivatization steps

    Final product types

    • Sartan antihypertensive APIs (e.g., Losartan intermediates)
    • Triazole antifungal precursors (e.g., Voriconazole intermediates)
    • Beta-adrenergic receptor antagonist intermediates

    2. Fine Fragrance Ingredient Manufacturing

    This material serves as a specialty intermediate in the synthesis of high-purity aromatic compounds and musks for the fragrance industry. 1-Phenyl-1,2-Ethanediol supports downstream processes requiring precise control over impurity profiles and reaction selectivity, providing a reliable route to key fragrance intermediates which define unique scent characteristics in luxury perfumery and cosmetic products. Its consistent quality supports stringent batch-to-batch reproducibility essential for established fragrance houses.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • ISO 9235:2013 (Aromatic natural raw materials and related substances)
    • REACH (EC) No 1907/2006 substance registration and assessment
    • Allergen labeling requirements under EU Cosmetic Regulation 1223/2009

    Typical usage ratio

    • 3–7% w/w of the fragrance intermediate synthesis batch; precise quantity adjusted for reaction yield and target olfactory profile

    Downstream process integration

    • Added during acetalization, cyclization, or etherification stages when constructing musks and complex esters; integrated before final distillation and purification

    Final product types

    • Macrocyclic musk intermediates
    • Fine perfumery bases (aldehyde-containing blends)
    • Premium personal care essence blends

    3. Polyurethane Elastomer Synthesis Additive

    In specialty polymers, 1-Phenyl-1,2-Ethanediol is utilized as a chain extender or modifier in polyurethane elastomer systems where enhanced flexibility and improved abrasion resistance are required. It reacts with isocyanates to influence microstructure and terminal group characteristics, affecting mechanical performance in high-wear industrial applications. Material addition optimizes hardness and elongation parameters, with strict process control ensuring end products consistently meet industrial safety and durability specifications.

    Industry compliance standards

    • ISO 9001:2015 (Quality management systems for polymer production)
    • REACH (EC) No 1907/2006 Registration – Industrial Polymers
    • EN 71-3:2019 (Safety of toys: migration of certain elements, for relevant consumer products)
    • ASTM D412 (Standard Test Methods for Vulcanized Rubber and Thermoplastic Elastomers – Tension)

    Typical usage ratio

    • 0.2–1.8% by total polyol mass; dosage adjusted based on required mechanical property targets such as tensile strength and elastic modulus

    Downstream process integration

    • Charged into the polyurethane reaction vessel post-polyol blending and prior to isocyanate addition; monitored for complete reaction through viscosity measurements

    Final product types

    • Industrial roller coatings
    • Flexible cable jacketing
    • Custom-molded polyurethane parts for mechanical and automotive applications

    4. Photoinitiator Synthesis for Specialty Coatings

    1-Phenyl-1,2-Ethanediol functions as a key synthetic precursor in manufacturing advanced photoinitiators used in UV-curable inks, adhesives, and high-performance coatings. Its molecular structure enables streamlined construction of benzoin-type photoinitiators, providing effective UV absorption and rapid polymerization capability. Stringent quality requirements for photoinitiator intermediates necessitate tight control of input material purity and trace impurity level, ensuring downstream manufacturers achieve specified cure rates and product consistency.

    Industry compliance standards

    • ISO 9001:2015 (Quality systems for chemical intermediates)
    • SGS EN 71-3 (materials in child-accessible coatings)
    • Directive 2004/42/EC (VOC content limits for coatings and inks)
    • RoHS Directive 2011/65/EU (hazardous substances restriction, electronics)

    Typical usage ratio

    • 5–12% molar ratio relative to benzaldehyde or photoinitiator core during photoinitiator synthesis batches; determined by target curing profile and solution viscosity

    Downstream process integration

    • Incorporated during mixed condensation or acetalization steps to produce photoinitiator intermediates; real-time reaction monitoring for purity and yield optimization

    Final product types

    • UV ink photoinitiators
    • UV-curable clear coatings for electronics and optics
    • Crosslinker additives for 3D printing resins

    5. Corrosion Inhibitor Intermediate for Metalworking Fluids

    This diol compound is employed as a synthetic intermediate in the preparation of complex organic corrosion inhibitors for advanced metalworking fluids. It participates in derivatization steps yielding chelating agents that shield ferrous and non-ferrous surfaces from oxidative degradation under stressing lubrication and cooling conditions. Purity and residual moisture levels directly impact inhibitor shelf-life and effectiveness in long-cycle machining and forming applications.

    Industry compliance standards

    • ASTM D4627 (Standard Test Method for Iron Corrosion Inhibitors in Hydraulic Fluids)
    • REACH Regulation (Annex XIV & XVII, substances in industrial lubricants)
    • ISO 6743-13:2002 (Classification of metalworking fluids)
    • OSHA Hazard Communication Standard (Material Safety Data requirements)

    Typical usage ratio

    • 1–4% by total inhibitor formulation mass, ratio tailored to fluid base composition and required corrosion protection duration

    Downstream process integration

    • Condensed with functional acids or amines during corrosion inhibitor synthesis; added pre-formulation into metalworking fluid concentrate blending tanks

    Final product types

    • Water-based and semi-synthetic metalworking fluid concentrates
    • Industrial lubricant packages for stamping and cutting operations
    • Hydraulic fluid additives for stationary and mobile equipment
    Free Quote

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    Certification & Compliance
    More Introduction

    1-Phenyl-1,2-Ethanediol: A Practical Commentary from an Experienced Chemical Manufacturer

    The Substance and Its Straightforward Nature

    1-Phenyl-1,2-Ethanediol always draws attention in the synthetic arena. This colorless to pale yellow diol, also known by its CAS number 93-56-1, holds an honest place among small, versatile building blocks in the organic toolbox. Our production line handles it routinely, and the molecule’s character becomes apparent as soon as one works with it in practical settings. Unlike many reagents requiring special protocols or creating more problems than solutions, phenylethylene glycol’s reactivity remains direct. Its aromatic ring provides resonance stability, while the vicinal diol structure opens doors for functional transformations. The straightforwardness wins over both seasoned chemists and process engineers.

    Specifications: Purity and Physical Traits from the Source

    We make this product with a focus on clarity—meaning not in market hype, but in physical appearance and purity. Seeing the crystalline solid in bulk, the first thing to notice is absence of color, slight gloss, and consistent particle size, whether granulated for batch reactors or kept as flakes for easy weighing. Typical purity values through our standard routes rest at 99% or above, confirmed by in-house gas chromatography and HPLC records after every synthesis. Moisture content stays low, often below 0.2%, thanks to distillation over drying agents and simple, careful storage controls. Impurity profiles receive routine screening. We do not tolerate acetophenone or mono-alcohol carryovers, choosing to reprocess batches rather than create complications downstream.

    Production Details Reflecting Real Experience

    Our method uses standard phenyl ethylene oxide hydration, following a time-tested path, then works through liquid-liquid extraction and distillation steps where process improvements over years have minimized solvent residues. Temperatures remain steady, not swinging to extremes, which protects yield and consistency. During purification, operator know-how comes into play. It’s the set of small technical decisions on crystallization temperatures, distillation cut-off points, and filtered fines that separate a successful batch from a mediocre one. We see every kilogram produced as an outcome of real attention, not automation alone. Dealing with challenging lots or unusual feedstock quirks, we rely less on theoretical best cases and more on learned judgment.

    Applications: Foundation and Reliability across Fields

    Reaction labs see 1-Phenyl-1,2-Ethanediol as a dependable intermediate for pharmaceuticals and agrochemicals. Its diol group offers functional handles for cyclization and rearrangement. In practical medicinal chemistry, the molecule serves as a precursor to chiral drugs and building blocks. Custom synthesis projects often focus on using the 1,2-diol motif to introduce stereocenters. We’ve supplied it for scale-ups heading towards epoxide ring closures and complex oxidation steps. One batch ran straight into an anti-fungal azole synthesis, another into a veterinary compound.

    Fine chemicals producers value the way this glycol reacts under mild conditions, avoiding excessive byproducts. Polymer researchers target the rigid phenyl segment to tune glass transition temperatures of specialty resins. Compared with simple ethylene glycol, the phenyl version imparts greater rigidity, and our customers mainly want that extra stability in performance materials. In fragrance chemistry, this material forms a step in aromatic ester production—certain musky compounds gain both longevity and warmth from the intermediate’s skeleton.

    Comparison with Related Products—Real Distinctions

    Plenty of diols fill catalogs, but choice narrows quickly once process constraints come into play. Ethylene glycol may remain cheaper and more abundant, but its two-carbon backbone lacks the aromatic stabilization. It oxidizes easier under harsh conditions and breaks down faster in oxidative stress situations. Our work with both standard glycols and phenyl substitutions reveals clear differences: 1-Phenyl-1,2-Ethanediol resists decomposition better during strong oxidations and copes with more aggressive catalyst regimes—processes that leave plain ethylene glycol products burned or discolored.

    Compared with 1,2-cyclohexanediol or other cyclic versions, the aromatic nature of our product introduces π-stacking and other interactions valuable in supramolecular frameworks and specialty ligand design. There’s a tactile difference too—cyclohexyl versions tend to absorb moisture faster and cake when stored, while phenyl-1,2-ethanediol, especially in our tightly-sealed drums, keeps its crystalline texture even through seasonal climate shifts. Shelf life extends beyond twelve months if the packaging’s integrity is preserved. Processing staff prefer fewer clumps and easier dosing, day in, day out.

    Consistency: Why Real Manufacturing Matters

    Customers report major headaches when buying from traders who never see the product until it’s loaded for shipment. Offsite blending, relabeling, and dilution practices run risks that can ruin entire syntheses upstream. We run every batch from raw material evaluation through final packaging right at our own facility, without middlemen, using our own technicians for quality control and storage. A batch of 1-Phenyl-1,2-Ethanediol from us brings reassurance—GC purity traces, exact packing weights, and fresh silica desiccants. Shippers sometimes do not realize moisture pick-up can destroy a 100-kg drum left open for only an hour in the wrong warehouse. We respond to any claims with actual analysts from the production line, not a generic corporate desk.

    Supporting Industry and Research

    Feedback from both R&D departments and pilot plant operators cycles back to us quickly—those who scale from milligrams to multi-kilogram lots count on unambiguous composition and traceability. There was a run of chiral building block work from a client, where enantiomeric purity needed routine checking. We invested in more advanced chiral columns and modulated our synthesis routes to keep both enantiomers separately available. The dialogue between manufacturing and applied research never stays theoretical. We work with spectral libraries, not just carbon copies of published procedures, and we tell our partners directly if a process adaptation might affect selectivity or byproduct levels.

    A plant making specialty UV-stable polymers once relied on a similar diol, only to run into issues with yellowing and premature chain scission under stress testing. Our phenyl variant, thanks to its ring structure, held up better and provided a path to higher-durability plates. That feedback came via a direct report, and it drove us to tighten our pre-shipment testing. There’s no better proof of performance than a real part tested in the field or a batch of drug substance produced without purification headaches.

    Compliance and Transparency—Experience from Troubleshooting

    In recent years, sourcing confidence dropped across the sector due to confusion over origin, hidden fillers, and paperwork mismatches. We keep compliance straightforward. Every shipment comes with a batch-specific certificate that aligns with in-house LC/GC data. Shipping documents never list fictitious or offsite manufacturers. On occasion, regulatory forms add new requirements, such as hazard communication updates or shipping limits based on destination. Our compliance team handles the changes in stride—we believe in practical readiness, which includes clear labeling and full disclosure of trace impurities, no matter how minor. This approach heads off problems for formulators, especially those in the pharmaceutical zone where regulatory inspections can halt whole processes with a single discrepancy.

    There have been times incoming inspection teams at customer sites found mismatches with competitor’s labeling and test results. Our response stays simple—offer a direct connection to production records, access to working chemists, and, where needed, a resample from reserved retention lots. Practical transparency often speaks louder than certificates alone.

    Sourcing and Logistics—Learning from the Ground Up

    Long before global supply chain stories filled newsfeeds, we lived through delayed railcars and lost shipments firsthand. Experience led us to standardize robust packing—tight-seal solid containers, reinforced liners, moisture sensors for large drums—rather than saving a few cents on lighter barrels. Most claims about off-odors or dusty product come straight from careless repackaging or exposure in humid warehouses. Our drums stack neatly, vents work, and there’s direct traceability on every serial number printed. Overseas shipments present their own headaches, so we mark all drums with scannable batch codes and always ship on covered pallets. These precautions resulted from actual problems, not hypothetical checklists.

    Customers in the pharmaceutical industry especially demand repeatability for multiple-year projects. We maintain a set inventory buffer, keep production lots separate by campaign, and monitor warehouse temperature/humidity levels. Questions never have to wind through a reseller. They reach the same technical staff who filled the first order, equipped with batch test records stretching back years. This structure reduces confusion and keeps supply smooth.

    Safety Handling—A Grounded Perspective

    Researchers and technicians respect 1-Phenyl-1,2-Ethanediol for its low volatility and moderate toxicity profile. It does not require cold-chain storage, nor does it fume or off-gas under normal handling. Spills wipe up easily because the solid form limits spreading. But the diol, like most organic reagents, requires some common-sense precautions. Our own team works in ventilated stations, prefers nitrile gloves to avoid mild skin irritation, and always clean up with plenty of water on hand. Drums leave the plant labeled with all proper hazard statements, but from years on the floor, we know that accidents usually trace back to lapses in attention, not material surprises. Most issues disappeared after extra operator training and regular walk-throughs looking for bottlenecks.

    Solubility in polar solvents like water, ethanol, and acetone suits most equipment cleaning procedures, which our staff performs before and after every campaign. We emphasize these basics in every customer conversation, especially with new users accustomed to handling only off-the-shelf commodity chemicals. By sharing safety experiences openly, we have reduced near-misses for both customers and our own team.

    Potential and Opportunities for Downstream Innovation

    Discussions with long-term clients reveal ongoing trends—the move toward greener, more targeted syntheses puts molecules like 1-Phenyl-1,2-Ethanediol under a fresh spotlight. Its aromatic-diolic structure plays a role in biocatalysis and in enantioselective oxidations that larger industry players now adopt. Catalytic work, from homogeneous to solid-supported systems, often uses this small diol as a testbed for new couplings or oxidation pathways. Some have tried immobilizing the compound on silica matrices to create tunable stationary phases for chromatography.

    A routine highlight involves the fusion of this product with custom aldehydes, then onward through cyclization into new heterocyclic frameworks. Research groups use our batches for proof-of-concept work aiming at patent filings, and we answer requests for unusual particle morphologies or microcrystalline cuts. Our familiarity with both process needs and experimental ambitions means we can adapt—not by advertising catchphrases, but by having the equipment and personnel ready for specialty runs, alternative purifications, and quick feedback loops.

    Why Working Directly with a Manufacturer Makes the Difference

    We listen closely to our partners—and it seldom takes long to spot whether someone’s counted on a spec sheet or handled the substance in real life. Problems get solved faster where the line between manufacturing and application shrinks. In years past, a batch designed for a specific enantiomer led to dialogue about selective crystallization; another instance required removing trace sulfur contamination traced to a misbehaving valve seal on a reactor. Resolving those kinds of issues, short of production halts, means experience must outweigh slogans.

    There are plenty of warehouse-stored, repacked, and rebranded diols floating in global commerce. We urge customers to ask tough questions—origin, test logs, packaging, purification details. By speaking directly to the plant, not a desk, users get not only transparency, but support from people who think about these issues every day. Our best relationships come from these conversations, not glossy catalogs or bulk discount offers.

    Why 1-Phenyl-1,2-Ethanediol Stands Out Over Time

    Reflecting on years spent producing and supplying this product, the clearest advantage shows up in reliability. No synthetic route works as planned with fluctuating materials or vague supply networks. Downstream chemists, engineers, and formulators never have to gamble with the quality, variability, or trace composition of their diols. Direct feedback drives process improvements, from tighter quality boundaries to expanded physical forms tailored for specific reactors or custom lots prepared for rapid scale-up. Routine never turns rote—the compound always demands precision, but responds well to honest work.

    Our perspective comes from a mixture of long hours at the bench, problem-solving during batch scale-ups, and open customer exchanges. It has shaped a product line that engineers can trust, chemists can predict, and managers can source without supply chain headaches. 1-Phenyl-1,2-Ethanediol will keep its relevance across changing applications, from fine chemical innovation to production-scale pharmaceuticals, precisely because real manufacturing experience backs every shipment.