Cas no 69630-25-7 (L-Glutamine, ethylester)
L-Glutamine, ethylester Chemical and Physical Properties
Names and Identifiers
-
- L-Glutamine, ethylester
- Ethyl L-glutaminate
- L-GLUTAMINE ETHYL ESTER HCL
- L-Glutamine,ethylester
- glutamine-ethyl-ester
- ethyl (2S)-2,5-diamino-5-oxopentanoate
- (S)-Ethyl2,5-diamino-5-oxopentanoate
- AKOS015932777
- EN300-7816156
- (S)-Ethyl 2,5-diamino-5-oxopentanoate
- AKOS006276751
- ETHYL (2S)-2-AMINO-4-CARBAMOYLBUTANOATE
- 69630-25-7
- SCHEMBL1538915
- SQMPFRFYKISAHD-YFKPBYRVSA-N
-
- Inchi: 1S/C7H14N2O3/c1-2-12-7(11)5(8)3-4-6(9)10/h5H,2-4,8H2,1H3,(H2,9,10)/t5-/m0/s1
- InChI Key: SQMPFRFYKISAHD-YFKPBYRVSA-N
- SMILES: O(CC)C([C@H](CCC(N)=O)N)=O
Computed Properties
- Exact Mass: 174.10044231g/mol
- Monoisotopic Mass: 174.10044231g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 12
- Rotatable Bond Count: 6
- Complexity: 170
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 1
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: -1.2
- Topological Polar Surface Area: 95.4?2
L-Glutamine, ethylester Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-7816156-0.05g |
ethyl (2S)-2-amino-4-carbamoylbutanoate |
69630-25-7 | 95.0% | 0.05g |
$407.0 | 2025-02-22 | |
| Enamine | EN300-7816156-0.1g |
ethyl (2S)-2-amino-4-carbamoylbutanoate |
69630-25-7 | 95.0% | 0.1g |
$427.0 | 2025-02-22 | |
| Enamine | EN300-7816156-0.25g |
ethyl (2S)-2-amino-4-carbamoylbutanoate |
69630-25-7 | 95.0% | 0.25g |
$447.0 | 2025-02-22 | |
| Enamine | EN300-7816156-0.5g |
ethyl (2S)-2-amino-4-carbamoylbutanoate |
69630-25-7 | 95.0% | 0.5g |
$465.0 | 2025-02-22 | |
| Enamine | EN300-7816156-1.0g |
ethyl (2S)-2-amino-4-carbamoylbutanoate |
69630-25-7 | 95.0% | 1.0g |
$485.0 | 2025-02-22 | |
| Enamine | EN300-7816156-2.5g |
ethyl (2S)-2-amino-4-carbamoylbutanoate |
69630-25-7 | 95.0% | 2.5g |
$949.0 | 2025-02-22 | |
| Enamine | EN300-7816156-5.0g |
ethyl (2S)-2-amino-4-carbamoylbutanoate |
69630-25-7 | 95.0% | 5.0g |
$1406.0 | 2025-02-22 | |
| Enamine | EN300-7816156-10.0g |
ethyl (2S)-2-amino-4-carbamoylbutanoate |
69630-25-7 | 95.0% | 10.0g |
$2085.0 | 2025-02-22 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1875775-1g |
(S)-Ethyl 2,5-diamino-5-oxopentanoate |
69630-25-7 | 98% | 1g |
¥6355.00 | 2024-05-03 |
L-Glutamine, ethylester Related Literature
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Juan J. Sánchez,Miguel López-Haro,Juan C. Hernández-Garrido,Ginesa Blanco,Miguel A. Cauqui,José M. Rodríguez-Izquierdo,José A. Pérez-Omil,José J. Calvino,María P. Yeste J. Mater. Chem. A, 2019,7, 8993-9003
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Xixi Li,Nanwei Zhu,Ruohan Li,Qinpu Zhang Anal. Methods, 2020,12, 3376-3381
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P. K. Wawrzyniak,M. T. P. Beerepoot,H. J. M. de Groot,F. Buda Phys. Chem. Chem. Phys., 2011,13, 10270-10279
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Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?o Chem. Commun., 2015,51, 3993-3996
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Eunhak Lim,Jiyoung Heo,Seong Keun Kim Nanoscale, 2019,11, 11369-11378
Additional information on L-Glutamine, ethylester
Comprehensive Guide to L-Glutamine ethyl ester (CAS No. 69630-25-7): Properties, Applications, and Market Insights
L-Glutamine ethyl ester (CAS No. 69630-25-7) is a derivative of the amino acid L-glutamine, widely recognized for its role in protein synthesis and cellular metabolism. This compound, formed by the esterification of L-glutamine with ethanol, offers enhanced stability and bioavailability compared to its parent molecule. Researchers and industries favor L-Glutamine ethyl ester for its solubility in organic solvents, making it a versatile ingredient in pharmaceuticals, nutraceuticals, and research applications.
The growing interest in amino acid derivatives like L-Glutamine ethyl ester is driven by their potential in sports nutrition and gut health. With the rise of fitness enthusiasts and health-conscious consumers, questions like "How does L-Glutamine ethyl ester support muscle recovery?" or "Is L-Glutamine ethyl ester better absorbed than L-glutamine?" are trending in search engines. Studies suggest that the ethyl ester form may improve absorption rates, making it a preferred choice for dietary supplements targeting immune support and intestinal barrier function.
In the pharmaceutical sector, L-Glutamine ethyl ester serves as a key intermediate in drug development. Its ability to cross cell membranes efficiently has sparked investigations into therapies for metabolic disorders and neurological conditions. Recent publications highlight its role in peptide synthesis, where it acts as a protective group for the carboxyl function of L-glutamine. This application aligns with the increasing demand for custom peptide synthesis in biotech research.
Market analysis reveals a steady growth trajectory for L-Glutamine ethyl ester, particularly in North America and Europe. The compound's alignment with clean-label trends and plant-based formulations has expanded its use in functional foods. Manufacturers are responding to queries such as "Where to buy high-purity L-Glutamine ethyl ester?" by emphasizing GMP-certified production and third-party testing protocols. Sustainability-focused buyers frequently search for eco-friendly amino acid derivatives, prompting suppliers to adopt green chemistry principles in synthesis.
From a technical perspective, L-Glutamine ethyl ester demonstrates remarkable stability under physiological conditions, with research focusing on its pH-dependent hydrolysis characteristics. These properties make it valuable for controlled-release formulations—a hot topic in precision nutrition circles. Laboratory protocols often feature this compound in cell culture media optimization, addressing common search terms like "L-Glutamine ethyl ester protocol for mammalian cells."
Quality specifications for CAS No. 69630-25-7 typically require ≥98% purity by HPLC, with strict limits on residual solvents. Analytical techniques such as NMR spectroscopy and mass spectrometry are employed to verify the ester's structural integrity—information frequently sought by quality control professionals. The compound's crystalline powder form and white to off-white appearance serve as visual indicators of purity, important for formulators troubleshooting solution clarity issues.
Emerging applications in cosmeceuticals have positioned L-Glutamine ethyl ester as a potential skin barrier enhancer. Dermatological studies explore its capacity to stimulate collagen production, coinciding with consumer searches for "anti-aging amino acid compounds." This intersection of biochemistry and personal care science demonstrates the compound's cross-industry relevance, particularly in multifunctional active ingredients for topical formulations.
Storage and handling recommendations for L-Glutamine ethyl ester emphasize protection from moisture and prolonged heat exposure—key considerations for stability maintenance. Technical documents often include solubility data in various solvents, responding to frequent queries about "L-Glutamine ethyl ester solubility in DMSO." These practical details support researchers in experimental design while optimizing the compound's performance in biological systems.
The scientific literature documents L-Glutamine ethyl ester's participation in transamination reactions and nitrogen metabolism pathways. These biochemical properties underpin its therapeutic potential, particularly in conditions involving cellular stress responses. Recent preclinical studies investigating gut-brain axis modulation have further elevated interest in this modified amino acid, with publication rates increasing by 22% year-over-year in relevant journals.
Regulatory status varies by region, with L-Glutamine ethyl ester generally recognized as compliant for research use under GLP guidelines. Manufacturers catering to global markets must navigate REACH compliance and FDA GRAS considerations—topics generating substantial search volume among compliance officers. Documentation packages typically include stability studies, impurity profiles, and toxicological assessments to meet diverse regulatory requirements.
Future research directions for CAS No. 69630-25-7 may explore its prodrug potential and targeted delivery systems, areas gaining traction in personalized medicine discussions. The compound's molecular flexibility allows for further derivatization, opening possibilities for structure-activity relationship studies. Such investigations respond to the scientific community's growing focus on amino acid-based therapeutics with enhanced pharmacokinetic profiles.
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