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2-Nitrophenethyl Alcohol

    • Product Name 2-Nitrophenethyl Alcohol
    • Alias beta-(2-Nitrophenyl)ethanol
    • Einecs 221-970-6
    • 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

    790719

    Chemical Name 2-Nitrophenethyl Alcohol
    Cas Number 612-20-2
    Molecular Formula C8H9NO3
    Molecular Weight 167.16 g/mol
    Appearance Pale yellow solid
    Melting Point 47-49 °C
    Boiling Point 174-176 °C at 15 mmHg
    Density 1.28 g/cm³
    Solubility In Water Slightly soluble
    Pubchem Cid 68299
    Smiles CC(C1=CC=CC=C1[N+](=O)[O-])O
    Inchi InChI=1S/C8H9NO3/c10-6-5-7-3-1-2-4-8(7)9(11)12/h1-4,10H,5-6H2

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

    Packing & Storage
    Packing The 2-Nitrophenethyl Alcohol is packaged in a 100g amber glass bottle with a secure screw cap, labeled with safety and handling instructions.
    Shipping 2-Nitrophenethyl Alcohol is shipped in tightly sealed, chemical-resistant containers to prevent leakage and contamination. It should be protected from direct sunlight, moisture, and incompatible materials. During transport, it is classified as a hazardous chemical, requiring appropriate labeling and adherence to regulations for handling, storage, and emergency measures in case of accidental release.
    Storage 2-Nitrophenethyl alcohol should be stored in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances like strong oxidizers and acids. Keep the container tightly closed and away from direct sunlight. Use chemically resistant containers and ensure proper labeling. Storage should be secure to prevent spills and minimize exposure to moisture or heat, which can destabilize the compound.
    Application of 2-Nitrophenethyl Alcohol

    Applications of 2-Nitrophenethyl Alcohol in Industrial Manufacturing

    As a direct producer of 2-Nitrophenethyl Alcohol, we supply this specialty intermediate to key industries demanding high purity and reliable performance. This section details specific downstream sectors, focusing on real-world formulations, compliance, usage, and process integration to meet industrial standards and production needs.

    1. Pharmaceutical Intermediate in Active Pharmaceutical Ingredient (API) Synthesis

    Specialty API manufacturers use 2-Nitrophenethyl Alcohol for constructing complex molecular backbones, especially in the development of nitro-aromatic pharmaceutical compounds. The pure alcohol form is essential during nitro reduction or side-chain attachment, providing clean conversions and high selectivity. The controlled inclusion of this intermediate ensures reproducibility and compliance in batch reactions, supporting rigid QC protocols around impurity profiles.

    Industry compliance standards

    • ICH Q7 GMP for API manufacturing
    • USP and EP monograph ingredient purity requirements
    • 21 CFR Part 211 (FDA)
    • REACH Registration (EU)

    Typical usage ratio

    • 0.5–2.5 molar equivalents, dependent on synthesis pathway and targeted yield; ratio adjusted based on impurity carryover and conversion efficiency in multi-step syntheses

    Downstream process integration

    • Added after initial condensation or amidation steps in API assembly
    • Used as a nucleophile or precursor in Grignard and reduction reactions
    • Reacted under controlled temperature and inert gas environment to minimize side reactions
    • QC sampling post-reaction to ensure residual intermediate removal

    Final product types

    • Nitro-aromatic drug building blocks
    • Beta-adrenergic agonists
    • Central nervous system (CNS) agents
    • Precursor molecules for investigational new drugs (INDs)

    2. Fine Chemical Production: Nitroaromatic Compound Manufacturing

    Chemical companies employ 2-Nitrophenethyl Alcohol to introduce specific functional groups onto aromatic rings, producing nitroaromatic compounds used as advanced intermediates. Controlled dosing allows for groups to remain intact during subsequent oxidation or halogenation, enabling precise functionalization and downstream extension for further chemical modification, supporting advanced material and dye production.

    Industry compliance standards

    • ISO 9001:2015 for quality management
    • REACH (EC/1907/2006) substance registration
    • Globally Harmonized System (GHS) classification and labeling
    • Responsible Care® management system

    Typical usage ratio

    • 3–8% w/w of reaction mixture, tuned to desired degree of nitration and specific molecular weight targets of downstream compounds

    Downstream process integration

    • Introduced during initial aromatic substitution or reduction stages
    • Serves as coupling partner for further functionalization
    • Integrated with automated dosing for batch and continuous-flow reactors
    • End-use in coupling, reduction, and functional group manipulation stages

    Final product types

    • Nitroaromatic dyes
    • Advanced intermediates for polymers
    • Pigment precursors for specialty inks
    • High-performance additives for coatings

    3. Agrochemical Intermediate for Growth Regulators

    2-Nitrophenethyl Alcohol acts as a key precursor in synthesizing plant growth regulators and select agrochemicals. Its minimal by-product profile supports clean synthesis workflows necessary for compliance and environmental management. Sophisticated batch refineries incorporate the material in coupling and reduction steps that yield bioactive compounds for regulated crop enhancement product lines.

    Industry compliance standards

    • FAO/WHO specifications for pesticide ingredients
    • EPA 40 CFR Part 180 (US agrochemical registration)
    • ISO 9001 traceability protocols
    • OECD Good Laboratory Practice (GLP) for testing substances

    Typical usage ratio

    • Exact quantity determined by stoichiometric requirement, often 1.0–1.3 equivalents per target molecule, varying with crop type and target region regulations

    Downstream process integration

    • Added in stepwise condensation or amidation reactions
    • Combined with co-catalyst systems for selective reduction
    • Integrated into continuous manufacturing for major product lines
    • Sampled post-purification for residual nitro compound testing

    Final product types

    • Auxin-like plant growth regulators
    • Nitro-aromatic-based pesticide intermediates
    • Seed treatment agents
    • Bioactive crop stimulants

    4. Specialty Polymer and Resin Modification

    High-performance material manufacturers utilize 2-Nitrophenethyl Alcohol as a functional additive or chain extender in specialty resin and polymer synthesis. It supports the introduction of pendant nitro groups or aromatic alcohol moieties, altering curing kinetics, crosslinking density, and mechanical properties. Incorporation during pre-polymerization offers fine control over the end-use performance of the final composite products, especially where controlled reactivity and custom functionality are critical to customer process lines.

    Industry compliance standards

    • ISO 9001:2015 certification for production control
    • EU Directive 2002/95/EC (RoHS) and REACH for material safety
    • ASTM D638 (polymer tensile property testing)
    • GHS safety labeling

    Typical usage ratio

    • 0.5–2.0% by weight of total polymer batch, adjusted by formulation for targeted molecular weight and crosslink functionality in final product

    Downstream process integration

    • Incorporated during oligomer pre-polymerization or direct in-situ resin modification step
    • Added with initiator and catalyst for controlled chain extension
    • Supports both batch and continuous extrusion processes
    • Material compatibility verified through pre-production pilot testing

    Final product types

    • Modified epoxy resins
    • Functionalized polyesters
    • High-temperature thermoset composites
    • Specialized laminates for electronics and coatings

    5. Analytical Reagent Formulation for Chromatographic Derivatization

    Laboratory and industrial reagent suppliers use 2-Nitrophenethyl Alcohol as a derivatizing agent in chromatographic analysis, especially for aldehyde and ketone sample identification. Its reactivity and high purity enable reliable standards preparation and batch-to-batch consistency. Production processes integrate this reagent under validated SOPs to ensure reproducibility and traceability in reference standard manufacture.

    Industry compliance standards

    • ISO/IEC 17025 for laboratory competence
    • OECD GLP for reagent manufacture
    • Supplier MSDS and COA traceability
    • REACH Annex II for reagent handling

    Typical usage ratio

    • 0.1–0.5% volume in sample or calibrant solution, defined by LOD/LOQ requirements and matrix effects during method validation

    Downstream process integration

    • Added in derivatization reactions prior to GC-MS or HPLC analysis
    • Prepared in high-purity solvents under clean-room conditions
    • QC testing for derivatization agent reactivity and purity on each batch
    • Stored and dispensed under inert atmosphere to avoid contamination

    Final product types

    • Certified reference materials (CRM)
    • Analytical standards kits
    • Specialty testing reagents for chromatography
    • Derivatized environmental or food safety samples
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    Certification & Compliance
    More Introduction

    2-Nitrophenethyl Alcohol: A Manufacturer’s Perspective

    The Realities of Producing 2-Nitrophenethyl Alcohol

    Years of close work in aromatic alcohols have shown me how demanding purity can be. 2-Nitrophenethyl Alcohol isn’t your typical building block. In our plant, it comes out as a pale yellow to nearly clear liquid, with a subtle, recognizable scent – and though that aroma fades during downstream use, it gives glimpses into its underlying chemistry every step along the line.

    Model: 2-Nitrophenethyl Alcohol, molecular weight 153.15, CAS number 612-28-2. The nitro group’s position matters. Our technicians keep a close watch on positional isomer content. We see the difference between products that pass a simple quality test and those that meet the high bar for fine chemicals, pharmaceuticals, or materials science.

    What Sets the Production of 2-Nitrophenethyl Alcohol Apart?

    Anyone making small aromatic alcohols at industrial scale knows the headache of keeping by-products at bay. Trace impurities complicate nearly every application, but for 2-Nitrophenethyl Alcohol, even a small deviation in nitro placement means a different compound. Other manufacturers sometimes offer phenethyl alcohols with mixed isomers. Our approach has always emphasized careful precursor selection and process control, so the final material is nearly free of 4-nitro or 3-nitro contamination.

    Here, the nitro group sits in the 2-position, opening up a set of characteristics that the other isomers simply don’t show. Its hydroxyl group offers avenues for further functionalization, and the ortho-nitro group’s electron-withdrawing effect changes reactivity completely compared to, say, phenethyl alcohol or even 4-nitrophenethyl alcohol. We talk to chemists who work with both, and they always tell us how a subtle structure shift means the difference between a successful synthesis and a wasted lot of material. We’ve seen the extra steps saved by using a pure 2-nitro derivative — no need to separate isomers downstream, no ambiguity about which product enters the next reaction.

    Why Do Chemists Seek This Niche Material?

    We work with people pushing the bounds of what aromatic building blocks accomplish. The big demand for 2-Nitrophenethyl Alcohol doesn’t always show up in commodity markets — it’s too specialized for that. Its unique position on the benzene ring makes it an important intermediate for pharmaceutical research, high-value specialty chemicals, and new materials destined for next-generation data storage or optoelectronic devices. A classic use: as a starting point for preparing ortho-substituted phenethylamines, where any deviation creates regulatory issues or throws off biological activity.

    I’ve spent days in discussions with synthesis teams refining custom pathways. Some tell us straight: only ortho-nitration gives the scaffold they need for their target molecules. Others want to further reduce or substitute the nitro group, and starting with compromised or mixed isomers just brings frustration. We keep our batches consistent, making life easier down the line, saving cleanup and allowing more reliable results every time.

    The Challenge and Value of High Purity

    Manufacturers aren’t always eager to discuss what makes a “high-purity” 2-Nitrophenethyl Alcohol, but experience dealing with feedback from the lab bench taught me: even 0.5% isomer impurity can show up in chromatography, then confound biological screening or material property testing. The purer our output, the smoother every application runs.

    Our batches are routinely analyzed by GC and NMR for isomer content. Customers with fussy downstream requirements send us questions about possible residual solvents, trace starting material, or odd by-product peaks. The fewer the questions, the more confidence our process controls inspire. The trust is mutual: nobody enjoys a frustrated chemist discovering an overlooked impurity only after weeks of scale-up.

    Handling and Shelf Stability in Real Conditions

    After years of handling bulk containers and small bottles, I can confirm that true 2-Nitrophenethyl Alcohol is reasonably stable under normal storage conditions. Still, like other nitroaromatics, it reacts unhappily with strong base, excess heat, or sunlight. Shelf stability improves with careful bottling in amber glass or pails, with oxygen-excluding caps. We minimize batch exposure to air, and never mix container material unless we have long-term data showing stability. Our experience led us to avoid tin or soft plastics, which can discolor or degrade the product faster than expected.

    Easy to pour, this alcohol dissolves cleanly in standard organic solvents: ether, methanol, a host of chlorinated and aromatic hydrocarbons. Our distributors say it ships well when packaged right, but we always advise careful secondary containment in high-volume shipments. Avoiding stress, agitation, excessive light, or heat during transit keeps every batch as consistent as the day it left our plant.

    Direct Comparison with Related Compounds

    If you look at ordinary phenethyl alcohol — often used in fragrances or as a food additive — you’ll see it lacks the powerful electron-withdrawing nitro group. That means reactivity is entirely different. 2-Nitrophenethyl Alcohol undergoes reductions, substitutions, and nucleophilic attacks in ways the unsubstituted alcohol never will. We often help explain to partners: don’t expect the same downstream chemistry.

    Move the nitro to the 4- (para) position and you get 4-nitrophenethyl alcohol, which serves a different market, with its own regulatory and process concerns. The ortho effect isn’t trivial: hydrogen bonding, steric hindrance, overall reactivity — the position translates into entirely different intermediate properties. Any formulation or process that depends on precise site reactivity fails if isomers get mixed.

    We’ve also met buyers surprised by the subtle color difference. High-purity 2-nitro derivative runs lighter in color when kept from light and air. We avoid surface catalysis by keeping contact with inert liners, and rapid filtering at the last step ensures clarity. That level of quality comes from experience, not luck.

    The Small Scale Challenge: Quality Over Quantity

    Mass-market chemical manufacturers focus on throughput. By contrast, our runs prioritize quality, batch documentation, and traceability from raw materials through finished vials. Custom orders get closer analysis, with full spectral and chromatographic data on request. It’s not enough to ship the right label — it has to match high expectations, every time. We answer detailed questions about analytical methods, with teams ready to walk through data to confirm identity and purity.

    For small R&D groups, reliability makes all the difference. I’ve fielded emergency requests many times: a university can’t complete its synthesis, all because an off-the-shelf supplier mislabeled or didn’t separate isomers. That interruption wastes not just product, but scientific progress. Our approach always leans toward supporting scientific clarity, not just filling orders. That commitment takes more effort, but it pays back in long collaborations and word-of-mouth recommendations.

    Process Improvements: What the Field Requires

    The market for 2-Nitrophenethyl Alcohol doesn’t stand still. New regulations, higher analytical standards, and more demanding applications mean every batch gets tighter controls. The shift toward greener synthesis and precision catalysis means we’ve had to adapt. We no longer use old-school nitration routes with excess acids and hazardous waste streams. Instead, we use milder, stepwise nitrating agents and recycle as much as possible, all while keeping a close eye on isomer ratio and yield.

    Energy efficiency has become a major factor, not just for reducing cost, but also for meeting stricter environmental targets worldwide. Instead of outmoded washing steps, we switched to cleaner, solvent-minimizing extractions alongside high-efficiency purification. Where possible, we track carbon and waste footprints and send samples for independent review. That’s not marketing fluff; waste disposal costs are real, and every kilo of intermediates that doesn’t meet spec means avoidable reworking.

    Future Prospects and New Applications

    I regularly field requests from materials researchers hoping to coax new behavior from old scaffolds. 2-Nitrophenethyl Alcohol plays a role in novel polymers, small-molecule sensors, and precursors for medical imaging probes. Its capacity for downstream modification — especially the reduction of the nitro group to an amine — makes it stand out in heterocyclic chemistry. Some of our most innovative customers see it as a hidden workhorse: a stable group ready to carry transformations other intermediates simply can’t handle without collapsing or cross-reacting.

    Synthetic biology applications are growing, with researchers asking for ever-purer starting material to enable controlled enzyme catalysis or preparation of isotope-labeled analogs. Isotope enrichment makes things trickier, but our platform allows for custom orders with deuteration or C-13 incorporation, using tailored routes that cut cost and avoid cross-contamination.

    We’ve even participated in projects requiring microgram-to-gram runs for rare analogs, not just tons of standard product. Pure, well-characterized 2-Nitrophenethyl Alcohol serves as a key step for these boutique syntheses.

    Dealing with Global and Supply Risks

    Anyone in chemical manufacturing knows the uncertainty of global supply, shipping logistics, and interrupted access to precursors. 2-Nitrophenethyl Alcohol production depends on reliable sources for nitrobenzene derivatives — any hiccup in upstream sourcing means downstream delays, and quality can’t afford a drop, even if costs rise. We build in secondary supplier relationships, check purity from every new drum of input, and always keep several cycles’ worth of inventory on hand.

    Shipping challenges have only grown in recent years, with new labeling, reporting, and packaging requirements arriving almost every quarter. Our regulatory team stays updated to avoid shipment holds or customs snags. We train warehouse and handling teams to spot issues early, reducing risk of loss or compliance problems.

    Some buyers have been burned by cut corners: questionable origins, inconsistent paperwork, or suddenly unavailable batches. That may work for commodities, but for a product like 2-Nitrophenethyl Alcohol, it means lost time, lost research, and lost business. By sticking closely to documentation and QC routines, we minimize risk and back every batch with full traceability.

    Customer Partnerships Help Shape the Future

    We don’t just sell product — we serve as a sounding board and collaborator to dozens of innovation teams. Sometimes a process bottleneck leads to a new purification trick; sometimes feedback from a pilot plant sparks a modification for easier downstream handling or faster reaction time. With each long-term relationship, we’ve learned to anticipate requests: smaller batches for just-in-time R&D, or large-volume, prequalified stock for repetitive production.

    We respond directly to technical queries and troubleshooting — at times even before a formal inquiry comes in. Problems like off-odors, unexpected color shifts, or variance in solubility find fixes by working with those who know the compound at a fundamental level, not by referencing a generic spec sheet.

    By investing in our own synthesis and purification rather than outsourcing critical steps, we keep control over what our customers receive, making ad hoc adjustments possible much faster than with trading intermediaries. I’ve seen trust turn into ongoing partnerships, where open technical dialogue means each success leads to the next.

    2-Nitrophenethyl Alcohol and Regulatory Considerations

    We all operate under the cloud of chemical safety and regulatory oversight. 2-Nitrophenethyl Alcohol occupies a unique space: not a listed controlled substance, but a significant precursor for compounds that are. That reality places a higher burden on batch documentation, inventory tracking, and customer vetting. Every invoice and shipment gets logged, ready for inspection.

    Newer laws in major markets call for end-use declarations, tighter restriction of export destinations, and regular updates to safety data. We stay ahead by keeping documentation complete and current, training all staff, and informing customers about necessary paperwork before shipments leave our warehouse.

    With experience, we anticipate audit requests and verification steps. It’s not about bureaucracy — it’s about trust with both authorities and our partners. Surprises can lead to shipment holds or compliance cases, so we eliminate ambiguity from the start.

    Improving the Product, One Step at a Time

    As a team, we always look for ways to make the product easier to use and store. Customer feedback, plus our own field trials, drive upgrades in every lot. We invested in automated filling lines with nitrogen blanketing for better shelf life, added batch-level QR codes for easy traceability, and keep technical support just a call away. We retired certain outdated purification stages and now use multi-stage vacuum distillation to boost clarity and cut trace residuals.

    These fixes sound simple on paper but save our partners much time and cost at the bench later. Fewer headaches, fewer unknowns, tighter analysis — that’s the real progress, evidenced by more successful projects down the line.

    Every product shipped carries not just our brand, but years of iteration, field problem solving, and real communication with the scientists, engineers, and innovators who rely on us. Our work never stops, because neither does theirs.