|
HS Code |
186786 |
| Product Name | Bz-Glu-OH |
| Iupac Name | N-benzoyl-L-glutamic acid |
| Cas Number | 2548-44-3 |
| Molecular Formula | C12H13NO5 |
| Molecular Weight | 251.24 |
| Appearance | White to off-white crystalline powder |
| Solubility | Slightly soluble in water, soluble in methanol and ethanol |
| Melting Point | 146-149°C |
| Storage Conditions | Store at 2-8°C, protected from light |
| Purity | Typically ≥98% |
| Smiles | C1=CC=C(C=C1)C(=O)N[C@@H](CCC(=O)O)C(=O)O |
| Usage | Peptide synthesis intermediate |
As an accredited Bz-Glu-OH factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Bz-Glu-OH is supplied in a 5 g amber glass bottle with a screw cap, labeled with product details and safety information. |
| Shipping | **Bz-Glu-OH** is shipped in tightly sealed containers under dry and cool conditions to prevent moisture uptake and degradation. It is labeled according to chemical safety regulations and typically transported as a non-hazardous organic compound. Appropriate documentation and safety data sheets accompany the shipment to ensure regulatory compliance and safe handling. |
| Storage | **Bz-Glu-OH** (Benzoyl-L-glutamic acid) should be stored in a cool, dry place, protected from light and moisture. Keep the container tightly closed, at 2–8°C (refrigerator) for optimal stability. Avoid sources of heat and incompatible materials such as strong oxidizers. Ensure good ventilation in storage areas and label the container clearly to prevent accidental misuse or contamination. |
Applications of Bz-Glu-OH in Industrial ManufacturingBenzyl glutamate (Bz-Glu-OH) demonstrates specialized value across several high-precision industrial fields. As a dedicated manufacturer, we support multiple application tracks where this protected amino acid intermediate meets stringent process and quality protocols. Below you will find segmented use cases along with corresponding compliance, ratio guidelines, process steps, and types of end products delivered by our direct customers. 1. Peptide Synthesis for Pharmaceutical APIsBz-Glu-OH provides a protected glutamic acid residue, facilitating sequential peptide elongation in solid-phase and solution-phase synthesis. Major peptide drug makers rely on our material to prevent side reactions during coupling. It acts as a temporary protecting group for the α-amino and γ-carboxyl functional groups in multi-step API manufacturing. Downstream operations employ controlled deprotection and coupling conditions, typically in cGMP environments. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Synthesis of Modified BiopolymersProducers of specialty polyamides and polyesters use Bz-Glu-OH as a protected monomer to control the location of functional groups in the resulting polymer chains. In segmented copolymerization, it helps engineer tailored properties such as biodegradability and hydrophilicity. Our material’s high purity ensures no by-product interference in catalyst-initiated polymerizations and enables selective post-polymerization deprotection for advanced material performance. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Advanced Research Reagents for Proteomics and Drug DiscoveryResearch institutions and custom synthesis labs require Bz-Glu-OH for incorporation into oligopeptide libraries and probe molecules designed for target validation, receptor studies, and structure-activity research. Its orthogonal protecting group strategy allows for precise building block selection under automated synthesizer and manual bench-scale chemistry, supporting both high-throughput screening and targeted assay development. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Chiral Building Block in Agrochemical SynthesisAgrochemical companies utilize Bz-Glu-OH as a chiral synthon to construct enantioselective intermediates in the production of herbicidal and pesticidal actives. Controlled protection of the glutamic acid group minimizes racemization and side reactions in asymmetric synthesis pathways. The material’s traceable manufacturing origin and batch-to-batch reproducibility meet strict documentation and impurity limits in regulated agrochemical pipelines. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Specialty Enzyme Substrate SynthesisManufacturers of biochemical diagnostic kits and activity assays incorporate Bz-Glu-OH for the custom preparation of enzyme-specific substrates. The benzyl protection aids selective coupling to chromogenic or fluorogenic reporter groups, ensuring defined substrate structure and purity. Our controlled processes prevent cross-contamination and provide clear analytical traceability, supporting critical QC requirements in regulated diagnostics supply chains. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive Bz-Glu-OH prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Our journey with N-Benzoyl-L-glutamic acid, known as Bz-Glu-OH, started out of necessity. In early days of custom peptide synthesis, we kept running into issues with inconsistent yields and unwanted side products. We aimed for greater control over protecting groups, so we invested in improving our manufacturing process for amino acid derivatives like Bz-Glu-OH. Careful attention to each reaction stage makes a difference in the purity and handling of every batch we produce.
Bz-Glu-OH plays a key role in solid-phase peptide synthesis and fragment coupling strategies. This compound carries a benzoyl group at the alpha-amino position of L-glutamic acid, leaving the side chain and carboxylic functions accessible. Over the years, researchers and manufacturers alike have relied on this structure for reducing side reactions during difficult couplings. We manufacture Bz-Glu-OH in batches of varying scales, always aiming for a purity exceeding 98%, confirmed by HPLC and NMR results. We have found that the downstream reproducibility depends heavily on this chemical integrity.
Specification sheets often don’t do justice to how the small details impact the synthesis outcome. We have learned that slight shifts in moisture content can affect stability or reactivity in solid-phase protocols. Controlling residual solvents, especially traces of chlorinated solvents or ether, pays dividends later. Our typical Bz-Glu-OH product appears as a white to off-white crystalline powder that dissolves smoothly in common organic solvents like DMF and DCM, which our team verifies batch-to-batch. Shelf-life studies show stability for several years in carefully sealed containers under cool, dry conditions—something we monitor by tracking batch samples in long-term storage.
We have plenty of experience scaling up for bulk lots, mostly for pharmaceutical and R&D labs, but occasional requests from universities keep us striving for flexible batch sizes. The melting range stands at about 171–174°C—a narrow range that acts as a good indicator of product cleanliness. Optical rotation can vary slightly by batch, so we check each to make sure we're still in line with published values for L-isomers. We have had customers design batch-to-batch chiral purity testing for us, which ultimately helped us refine our crystallization protocol long-term.
Glutamic acid derivatives present more challenges in process control than many people realize. During early development we struggled with byproduct removal, especially benzoylating agents that can linger if reaction conditions aren’t tightly held. Impurities from incomplete reaction led to problems in downstream coupling. Our solution involved stepwise washing, temperature-controlled quench, and a filtration approach refined over hundreds of runs. Our QA team found that UV and IR scan records were most predictive of trace impurity levels, rather than relying solely on HPLC reports.
Another concern comes from the physical properties—hygroscopicity becomes a problem in humid climates. We implemented dry-room packaging for every bulk drum to avoid clumping or hydrolysis before use. On several occasions, we worked with collaborators performing mass spectrometry to identify rare byproducts—less than 0.1% of peak area. These deep dives helped us trace the sources, like batch-specific secondary benzoylation, which we resolved by revisiting our agitation and cooling profile.
Bz-Glu-OH shows up on the bench whenever selective N-protection is needed. Research groups picking it for segment condensation value its ability to suppress racemization. Based on our experience, coupling steps using carbodiimide or phosphonium reagents run more smoothly with correctly protected glutamic acid derivatives. Many customers comment on the difference in purity between our Bz-Glu-OH and glutamic acid protected by simpler carbamates or phthalimide.
Benzoyl-protected glutamic acid shines in settings that require orthogonal deprotection—something crucial in assembling multi-step peptide chains. The benzoyl group stays robust when exposed to acidic TFA cleavage, so researchers can remove temporary side chain protections in parallel synthesis workflows without stripping the N-benzoyl group. After TFA, the benzoyl group comes off under milder conditions such as ammonolysis or catalytic hydrogenation, allowing the sequential construction of branched or complex targets. The reliability of this selectivity has made it a mainstay in our own synthesis lines for reference standards.
People sometimes ask why use benzoyl protection rather than Fmoc or Boc in peptide chemistry. In our experience, Bz-Glu-OH provides stability under acidic conditions that Fmoc cannot match. Boc groups tend to introduce more handling steps or come off under stronger acids, which adds risk for delicate peptide chains. The difference becomes clear with challenging sequences, or for solid-phase methods that require deprotection in the presence of side-chain-protected residues. In mass production or pharma settings, less side-product formation means less time in purification and better reproducibility between batches.
We see fewer diketopiperazine or oligomerization side reactions thanks to the reduced nucleophilicity of the benzoyl-protected amine. Years ago, our pilot plant compared batches made with Bz-Glu-OH and batches with standard Fmoc-Glu-OH. The HPLC data routinely showed that benzoyl batches required less preparative chromatography, saving on solvent and glassware cleaning cycles. Several clients now insist on Bz-Glu-OH for long-chain or hydrophobic peptides, where other protecting groups have failed.
There have been cases of lab teams underestimating the dusting potential of fine glutamic acid derivatives. Our staff wears particle-filtering masks and gloves during packing. Every pallet of Bz-Glu-OH comes in double-layer liners to avoid accidental exposure. We learned this early, after a batch lost some potency from extended open-air handling. The compound itself has low toxicity; routine chemical hygiene controls prove sufficient in regular use. Storage away from light and moisture goes a long way toward preserving product quality.
Disposal, especially for expired compounds or mother liquors, follows local chemical waste protocols. Our internal training emphasizes rinsing containers before recycling, which we track as part of our ISO-certified procedures. Plant staff continuously monitors storage area temperature and humidity, which prevents stock loss from caking or moisture contamination.
Many process improvements in our manufacturing started with feedback from clients encountering new challenges in their research. A university customer once flagged a problematic side-product, and together we adjusted our crystallization process to further boost purity. Another customer needed a batch at kilogram scale, but with tighter controls on residual benzoyl chloride. We implemented new batch monitoring for them. Every time new protocols or reagent needs arise, our technical team works alongside clients on custom specifications while maintaining batch-to-batch consistency.
Large pharmaceutical partners often develop proprietary synthetic routes that depend on reliable Bz-Glu-OH supply. We partner with these teams to share process improvements, review new analytical data, and prepare site audits that help everyone meet regulatory and quality targets. Experience tells us that keeping an open channel for technical exchange sustains both process gains and mutual trust. Solid supplier-customer collaboration drives new product development and ultimately raises the standard for peptide building blocks across the industry.
Regulatory demands have evolved, especially with changes in REACH and other global chemical management schemes. We updated our production systems to meet greater scrutiny over impurity profiles. Recently, increased pressure for green chemistry led us to evaluate solvents and waste streams. We have phased out chlorinated solvents wherever possible in the Bz-Glu-OH process, developing alternative washing protocols that achieve the same clean endpoint. These changes lower environmental impact without compromising product quality.
Our documentation now covers traceability for every batch of raw material and finished product. Annual reviews, as well as customer-initiated audits, help us identify further risk reduction opportunities. Each improvement in operational safety, solvent reduction, or staff training ultimately translates to higher batch reliability and wider acceptance in regulated markets. Adaptability and shared transparency keep everyone on safe and solid footing.
Interest in Bz-Glu-OH usage tracks with growth in biologics, peptide-based drugs, and high-throughput screening. Large-scale proteomics companies routinely request bulk material, citing a need for lower side-products in final peptide sequences. Contract development organizations have begun to request specialty grades tailored to automated batch processes. Many educational institutes continue to order smaller amounts for method development and curriculum studies.
We monitor research literature closely to spot shifts in protecting group preferences and solid-phase technologies. As non-natural amino acid incorporation grows, and multi-arm peptide scaffolds become more popular, we see new requests for analogs and customized protections. Staying ahead of these trends means ongoing investment in analytical methods and batch flexibility.
Chemical manufacturing doesn’t often get a spotlight, but our confidence in Bz-Glu-OH comes from countless real-world applications and problem-solving. Industry demands more reliability, higher purity, and secure supply. Each improvement to our Bz-Glu-OH process grows out of feedback from bench scientists, as well as the real constraints of plant operations. We believe customers benefit by working directly with the manufacturer—we keep our process open to technical scrutiny and keep pushing to refine what matters for peptide and pharmaceutical chemistry.
For us, the work never stops at one successful batch. As research demands grow and downstream requirements shift, we expect our processes and QC standards to evolve too. We have made Bz-Glu-OH a foundation of our amino acid derivatives product line, and we continue refining our methods so that the compound delivers consistent results in hands-on research, process chemistry, and commercial-scale synthesis. Our combined experience, from benchtop problem-solving to plant-scale optimization, keeps us focused on quality and innovation for every shipment.