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HS Code |
648883 |
| Product Name | Glycine N-Octyl Ester Hydrochloride |
| Cas Number | 67656-46-0 |
| Molecular Formula | C10H22ClNO2 |
| Molecular Weight | 223.74 g/mol |
| Appearance | White to off-white solid |
| Solubility | Soluble in water and organic solvents |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, in a tightly closed container |
| Ph 1 Solution | Around 4.5-5.5 |
| Synonyms | Glycine octyl ester hydrochloride; Octyl glycinate hydrochloride |
| Shelf Life | 2 years under recommended storage |
| Iupac Name | Octyl 2-aminoacetate hydrochloride |
As an accredited Glycine N-Octyl Ester Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of Glycine N-Octyl Ester Hydrochloride is supplied in a sealed, amber-glass bottle with tamper-evident cap and detailed labeling. |
| Shipping | Glycine N-Octyl Ester Hydrochloride is shipped in secure, airtight containers to prevent moisture absorption and degradation. The chemical is packed following safety regulations for hazardous substances, clearly labeled, and cushioned to avoid breakage during transit. Temperature and handling conditions are maintained as recommended to preserve chemical stability and integrity. |
| Storage | Glycine N-Octyl Ester Hydrochloride should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, and well-ventilated area, away from incompatible materials such as strong oxidizers. Recommended storage temperature is between 2–8°C (refrigerated). Ensure proper labeling and access only to trained personnel. Avoid prolonged exposure to air to prevent decomposition. |
Applications of Glycine N-Octyl Ester Hydrochloride in Industrial ManufacturingAs a direct manufacturer with decades of know-how in specialty amino acid derivatives, we supply Glycine N-Octyl Ester Hydrochloride (GNOEHCl) for strictly controlled downstream industrial markets. This section presents real-world adoption scenarios backed by regulatory standards, precise formulation ratios, integration techniques, and examples of commercial-grade finished products. Each field below reflects authentic application based on our customer partnerships and ongoing production feedback. 1. Chiral Intermediate for Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical manufacturers use GNOEHCl as a key chiral building block during the multi-stage synthesis of enantiomerically pure APIs, particularly in peptidomimetic drug classes. Its consistent quality and effective participation in controlled amidation and coupling reactions play a critical role in structure-specific transformations for patent molecules. Integration typically arises at the early route-design stages, supporting pathway optimization for regulated drug submissions. Industry compliance standards
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2. Surfactant Precursor in Specialty Cleaning AgentsChemical companies leverage GNOEHCl as a starting material to synthesize advanced cationic surfactants used in institutional and industrial cleaners. The compound's structure, featuring a glycine backbone and an octyl side chain, brings both hydrophilic and lipophilic balance ideal for formulation of residue-free, low-foaming surfactant systems targeting food processing equipment and high-throughput manufacturing environments. Industry compliance standards
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3. Cosmetics: Functional Additive in Premium Hair Conditioning FormulasPersonal care producers utilize GNOEHCl as a specialized functional additive in silicone-free hair conditioning and detangling treatments, capitalizing on its amphiphilic composition to improve texture, shine, and manageability without heavy buildup. Its compatibility with cationic emulsion systems facilitates gentle deposition onto hair fibers during conditioning, with dosing closely regulated to maintain safety and performance compliance across different global markets. Industry compliance standards
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4. Analytical Reagent Manufacturing for High-Performance Liquid Chromatography (HPLC)Lab chemical producers incorporate GNOEHCl as a derivatizing agent in HPLC sample prep kits, specifically for enantioselective and peptide analysis. Its introduction enables precise structural differentiation of amino acid-containing analytes through ion-pair or pre-column derivatization techniques, making it a reliable component for reference-grade analytical reagent sets distributed to pharmaceutical and food quality control laboratories. Industry compliance standards
Typical usage ratio
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As a chemical manufacturer with decades invested in research and hands-on production, we recognize the changing demands across both life sciences and specialty synthesis. One compound that continues to receive attention in recent specialty chemical development is Glycine N-Octyl Ester Hydrochloride. Delivering this product places us a little further inside the progress shaping modern biochemistry, drug delivery, and advanced research tools.
Glycine N-Octyl Ester Hydrochloride appeals to researchers and developers who search for clean, predictable esterification routes while working with amino acid derivatives. This compound combines the simplicity of glycine's base structure with the added value of a straight-chain octyl group, forming an ester suited for more hydrophobic settings. Unlike unmodified glycine, our ester hydrochloride yields a molecule with greater solubility in certain organic phases, along with improved membrane interaction. To the chemist on the bench, this means easier incorporation into lipid micelles, nanoformulation carriers, or analytical platforms where water solubility needs to be dialed down.
In our hands, the preparation of this ester is not merely a matter of following established literature. The process takes skill, strict quality control, and a solid appreciation for batch-to-batch consistency. We have refined each stage: from esterification to acidification, every variable—temperature, solvent system, catalyst use—plays a part in guarantee of the final purity. Our model batches routinely exceed 98% purity by HPLC, paired with low residual solvent content. This tight control suits both small-scale researchers mapping out peptide mimetics, and industrial groups investigating new excipients or delivery agents.
Chemically, lengthening the alkyl chain in amino acid ester derivatives has proven significance. The octyl group, compared to standard methyl or ethyl esters, extends lipophilicity in a predictable, linear fashion. Glycine N-Octyl Ester Hydrochloride does not behave like simple methyl glycine ester hydrochloride—its octyl tail imparts meaningful changes in interaction with hydrophobic media.
In practical terms, this means the compound supports formulations where amphiphilicity matters. Our clients in pharmaceutical research use it to simulate conditions for prodrug strategies, where transport across lipid barriers is a focal point. It also finds use in mixed surfactant systems, where balancing the hydrophilic-lipophilic properties gives rise to stable emulsions and vesicles. A molecule that carries a glycine head with an eight-carbon tail will insert into membranes but not as aggressively as a purely hydrophobic chain. This subtlety can affect drug release profiles, absorption behavior, and ultimately the predictability of results in both in vitro and animal testing.
Compared to other N-alkylated glycine esters, the octyl chain offers a sweet spot. Shorter chains (methyl, ethyl, propyl) produce too little membrane affinity, while longer chains such as dodecyl can introduce issues with aggregation or solubility loss in organic solvents. Our experience suggests the octyl version treads the line between necessary solubility and appropriate hydrophobic interaction, producing a balance that opens up new avenues for controlled transport and targeted biochemical interactions.
In the production process, the origin and handling of raw materials often dictate both the quality and reproducibility of the final ester. Over time, we have observed that even trace impurities in starting glycine or n-octanol can spiral into unwanted byproducts or difficulty in purification. For us, sourcing those components remains as important as the subsequent steps. Reactions are conducted under nitrogen, temperatures are monitored by both automated and manual means, and all batches undergo multiple purification cycles to rid traces of starting acid or alcohol.
Color and odor changes provide signals—too often ignored by new entrants—about the state of reactions. The evolution of a faint yellow tinge, for example, can point to over-heating or side-chain degradation. By careful monitoring and adjustment, we keep our product clear and stable, ensuring long shelf life for those buying in bulk.
We also take pride in the safety profile supported by analysis post-synthesis. Each manufacturing cycle ends with a comprehensive check for chloride content and amine impurities—common pitfalls that impact both shelf stability and application compatibility. This attention pays dividends for our customers: lower risk of side reactions during downstream synthesis, reduced batch rejection for pharmaceutical users, and improved reliability for researchers who need reproducible baselines in their experiments.
Glycine N-Octyl Ester Hydrochloride does not remain confined to the world of academic inquiry; it finds real value in several fields. In peptide and peptidomimetic development, its ester function acts as a temporary protecting group, removed under controlled hydrolysis at a later stage. The octyl tail shields the carboxyl group, allowing for sequential peptide assembly where traditional methyl groups fail to provide the needed hydrophobic interactions.
Drug delivery research also leans on this molecule, leveraging the enhanced lipid solubility to ferry actives across membranes. Our clients who test new prodrug candidates favor a construct that mimics or anticipates the challenges of absorption and transport inside biological systems. With this molecule, studies can approximate the balance between aqueous and organic solubility, yielding a more accurate forecast for actual performance inside the body.
Outside biochemistry, some teams exploit its surfactant-like properties. In emulsion polymerization, for example, the octyl ester supports the dispersion of otherwise water-insoluble agents. The hydrochloride counterion lends stability during high-shear mixing, leading to reproducible and stable emulsions—qualities valued in automotive coatings and high-performance lubricants. At pilot and commercial scales, we have observed the ease of integration and the improvement in both shelf stability and application uniformity.
Practical experience with Glycine N-Octyl Ester Hydrochloride reveals the stability one can get with proper handling. This material tolerates moderate swings in temperature so long as it remains sealed from atmospheric moisture. Absorbed water can shift the hydrochloride equilibrium and, in severe conditions, might drive hydrolysis or clumping. Thus, we package all output in low-moisture containers, filled under argon flow to maintain low residual oxygen and water vapor.
In our storage studies, batches stored at room temperature in amber glass or polyethylene containers remain usable for periods exceeding 18 months. No crystallization, sticky residue, or decomposition was found so long as external humidity does not reach the sample. Solutions like these, developed through routine and extensive stability studies, save clients from unexpected delays caused by product degradation or rework.
Real traceability matters—not only to auditors but to lab technicians. From the first kilo to the multi-ton scale, our logs document supplier batches, test results, and process deviations. Each shipment includes a full analytical suite: 1H NMR, 13C NMR, HPLC, and Karl Fischer titration for moisture. Many years of supplying large pharma, small biotech, and university labs place us in a position to understand what isn’t negotiable. Consistency keeps research on track, prevents failed syntheses and scale-ups, and underpins regulatory submissions where the burden of proof sits squarely with the producer.
Batch records show that even slight changes in the catalyst ratio or reactor pressure can shift the impurity profile. Our laboratories follow a regimen of reviewing both new and archived results when process improvements are considered, ensuring that modifications never compromise the standard researchers and end-users expect.
Some competitors focus on throughput or price, scaling up traditional methyl and ethyl glycine esters for commodity use. We have seen how those molecules can work in some routine syntheses. Glycine N-Octyl Ester Hydrochloride, by contrast, suits applications where chain length and moderate amphiphilicity play a direct role in outcome: for example, in sustained release formulations, specialized phase transfer catalysis, or as membrane mimics in biophysical studies. This ester, once a laboratory curiosity, has become a go-to building block for those needing nuanced control over solubility and molecular recognition.
Laboratory teams pushing boundaries in peptide chemistry see just how poorly simple methyl or ethyl esters fit into new drug delivery architectures. The octyl variant avoids the excessive stickiness of hexadecyl and the insolubility pitfalls of shorter chains, leading to more predictable behavior both during synthesis and later formulation steps. It neither precipitates out too quickly nor leaches dangerously into hydrophobic matrices. Each of these small shifts generates tangible benefits in both efficiency and final application performance.
We have collected input from both industrial and research users over many years. One theme surfaces repeatedly: Reproducibility in downstream reactions depends on subtle factors—impurity levels, ionic content, and raw material traceability. Early adopters sometimes assumed any alkyl glycine ester would deliver similar results. Our technical team worked side by side with partners, uncovering that uncontrolled batches or inconsistent processing led to incomplete reactions, lower yields, or phase-separation headaches in emulsions.
One pharmaceutical research group experienced shifting absorption rates in animal studies when switching between different ester grades from less reputable sources. Only after moving to our controlled, lot-traceable Glycine N-Octyl Ester Hydrochloride did absorption profiles align with their in silico predictions. These real-world experiences reinforce the importance of manufacturing discipline at every level.
Sustainability matters to us and to our long-term clients. Strict control of solvents and energy use during synthesis trims both cost and impact. By reclaiming process solvents and optimizing purification steps, we lower the disposal burden and keep waste streams narrow. No unchecked organics leave our plant: every batch of mother liquors is processed for recovery or neutralization. This responsible approach shortens the route from lab to production scale for customers seeking both regulatory compliance and low-environmental impact sourcing.
Given the applications in pharmaceutical intermediates and specialty surfactants, trace contaminants and documented residuals are non-negotiable. Our analytical team prepares regulatory support files—everything from impurity profiles to solvent residue declarations—on every production run. These efforts, instituted long before they were suggested by inspectors or regulatory authorities, now help clients speed up their own filings and keep surprises out of scale-up projects.
Over time, Glycine N-Octyl Ester Hydrochloride has moved from an interesting molecule into a true enabler for method development and finished product innovation. Each new customer brings unique approaches and requests. Our R&D team enjoys these challenges, whether finding tailored solutions for a novel nanoemulsion or troubleshooting analytical issues in peptide chain extension. We welcome these conversations, recognizing they push industry forward and help us remain at the forefront of specialty ester manufacturing.
From our perspective as long-term manufacturers, Glycine N-Octyl Ester Hydrochloride stands out by delivering the reliability, physical properties, and traceability modern researchers and process engineers demand. Every improvement we make comes from lessons learned in the field, in the plant, and with the partners who rely on us for both the expected and the unforeseen. Those who look past standard commodities and toward products shaped by consistency, expertise, and real-world feedback find value in every batch that leaves our facility.