Cas no 5794-13-8 (L(+)-Asparagine monohydrate)
L(+)-Asparagine monohydrate Chemical and Physical Properties
Names and Identifiers
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- (S)-2,4-Diamino-4-oxobutanoic acid hydrate
- L-2-Aminosuccinamic acid monohydrate
- H-Asn-OH.H_2O
- L-Asparagine monohydrate
- H-Asn-OH.H2O
- H-Asn-OH*H2O
- L-2-Aminosuccinamic acid
- L(+)ASPARAGINE
- L-Asparagine
- ASPARAGINI
- ACID SEMIAMIDE
- ASPARAGINIC ACID SEMIAMIDE MONOHYDRATE
- ASPARAGINE MONOHYDRATE
- ASPARAGINE H2O
- H-ASN-OH H2O
- H-L-ASN-OH H2O
- L-ALPHA-AMINOSUCCINAMIC ACID, MONOHYDRATE
- L-ASN H2O
- L-(+)ASPARAGINE HYDRATE
- L-ASPARAGINE HYDRATE
- L-ASPARAGIN MONOHYDRATE
- L-ASPARAGINE H2O
- L-ASPARTIC ACID 4-AMIDE MONOHYDRATE
- l-2-aminosuccinamic acid hydrate
- L-2-AMINOBUTANEDIOIC ACID MONOHYDRATE
- (S)-(+)-ASPARAGINE MONOHYDRATE
- (S)-2-AMINOSUCCINIC ACID 4-AMIDE MONOHYDRATE
- l-asparginemonohydrate
- (S)-(+)-2-Aminosuccinamic acid
- L-(+)-Asparagine monohydrate
- CultureSure L-Asparagine Monohydrate, Animal-derived-free
- H-Asn-OH · H?O
- H-Asn-OH·H?O
- L(+)-Asparagine monohydrate
- L-Asparagine.H2O
- Aminoplasmal
- Asparagen
- h-asn-oh.h
- H-Asn-OH·H2O
- L-Asp.H2O
- L-Asparagin,Monohydrat
- L-Asparagine anhydr.
- L-ASPARAGINE H20
- monohydr.
- H-Asn-OH Monohydrate
- L-Asparagine, monohydrate
- L-Aspartic acid 4-amide
- Asparagine [NF]
- asparagine
- (S)-2-Aminosuccinic acid 4-amide
- L(+)-Asparaginemonohydrate
- Asparagine (NF)
- 2PD79VF521
- C4H8N2O3.H2O
- Nutrifundin
- Thomaeamin
- Normofundin
- L(+)-Asparagine
- CultureSure? L-Asparagine Monohydrate, Animal-derived-free
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- MDL: MFCD00151038
- Inchi: 1S/C4H8N2O3.H2O/c5-2(4(8)9)1-3(6)7;/h2H,1,5H2,(H2,6,7)(H,8,9);1H2/t2-;/m0./s1
- InChI Key: RBMGJIZCEWRQES-DKWTVANSSA-N
- SMILES: O([H])C([C@]([H])(C([H])([H])C(N([H])[H])=O)N([H])[H])=O.O([H])[H]
- BRN: 5767869
Computed Properties
- Exact Mass: 150.06400
- Monoisotopic Mass: 150.064
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 4
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 10
- Rotatable Bond Count: 3
- Complexity: 134
- Covalently-Bonded Unit Count: 2
- Defined Atom Stereocenter Count: 1
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: 0
- Tautomer Count: 2
- Topological Polar Surface Area: 107
Experimental Properties
- Color/Form: Not determined
- Density: 1.543
- Melting Point: 233-235?°C (lit.)
- Boiling Point: 438°C at 760 mmHg
- Flash Point: 218.7°C
- Refractive Index: 31 ° (C=10, HCl)
- PH: 4.0-5.5 (20g/l, H2O, 20℃)
- Solubility: H2O: 20?mg/mL
- Water Partition Coefficient: 30 g/L (20 oC)
- PSA: 115.64000
- LogP: -0.39000
- Solubility: Not determined
- Merck: 837
- Specific Rotation: 35 o (c=10, 6N HCl)
- Sensitiveness: Sensitive to light
L(+)-Asparagine monohydrate Security Information
- Signal Word:Warning
- Hazard Statement: H315; H319; H335
- Warning Statement: P261; P264; P271; P280; P302+P352; P304+P340; P305+P351+P338; P312; P321; P332+P313; P337+P313; P362; P403+P233; P405; P501
- Hazardous Material transportation number:NONH for all modes of transport
- WGK Germany:1
- Hazard Category Code: 20/21/22-36/37/38
- Safety Instruction: S24/25
-
Hazardous Material Identification:
- Safety Term:S24/25
- Risk Phrases:R20/21/22
- TSCA:Y
- Storage Condition:Store at room temperature
L(+)-Asparagine monohydrate Customs Data
- HS CODE:2924199090
- Customs Data:
China Customs Code:
2924199090Overview:
2924199090. Other acyclic amides(Including acyclic carbamates)(Including its derivatives and salts). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%
Declaration elements:
Product Name, component content, use to, packing
Summary:
2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
L(+)-Asparagine monohydrate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| HE FEI BO MEI SHENG WU KE JI YOU XIAN ZE REN GONG SI | TA2275-100g |
L(+)-Asparagine monohydrate |
5794-13-8 | ≥99% | 100g |
¥70元 | 2023-09-15 | |
| HE FEI BO MEI SHENG WU KE JI YOU XIAN ZE REN GONG SI | TA2275-25g |
L(+)-Asparagine monohydrate |
5794-13-8 | ≥99% | 25g |
¥30元 | 2023-09-15 | |
| HE FEI BO MEI SHENG WU KE JI YOU XIAN ZE REN GONG SI | TA2275-500g |
L(+)-Asparagine monohydrate |
5794-13-8 | ≥99% | 500g |
¥240元 | 2023-09-15 | |
| BAI LING WEI Technology Co., Ltd. | 280618-25G |
L-Asparagine monohydrate, 98% |
5794-13-8 | 98% | 25G |
¥ 92 | 2022-04-26 | |
| BAI LING WEI Technology Co., Ltd. | 280618-100G |
L-Asparagine monohydrate, 98% |
5794-13-8 | 98% | 100G |
¥ 139 | 2022-04-26 | |
| BAI LING WEI Technology Co., Ltd. | 280618-500G |
L-Asparagine monohydrate, 98% |
5794-13-8 | 98% | 500G |
¥ 388 | 2022-04-26 | |
| DC Chemicals | DCT-031-20 mg |
L(+)-Asparagine monohydrate |
5794-13-8 | >98%, Standard References Grade | 20mg |
$280.0 | 2022-02-28 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | A108223-100g |
L(+)-Asparagine monohydrate |
5794-13-8 | 99% | 100g |
¥58.90 | 2023-09-04 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | A108223-10g |
L(+)-Asparagine monohydrate |
5794-13-8 | 99% | 10g |
¥29.90 | 2023-09-04 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | A108223-2.5kg |
L(+)-Asparagine monohydrate |
5794-13-8 | 99% | 2.5kg |
¥667.90 | 2023-09-04 |
L(+)-Asparagine monohydrate Suppliers
L(+)-Asparagine monohydrate Related Literature
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Christopher B. Rodell,Christopher B. Highley,Minna H. Chen,Neville N. Dusaj,Chao Wang,Lin Han,Jason A. Burdick Soft Matter, 2016,12, 7839-7847
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M. Zeiger,N. J?ckel,P. Strubel,L. Borchardt,R. Reinhold,W. Nickel,J. Eckert,V. Presser,S. Kaskel J. Mater. Chem. A, 2015,3, 17983-17990
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Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
Additional information on L(+)-Asparagine monohydrate
Introduction to L(+)-Asparagine Monohydrate (CAS No. 5794-13-8)
L(+)-Asparagine monohydrate, with the chemical formula C?H?NO?·H?O, is a widely recognized compound in the field of pharmaceuticals, biotechnology, and food science. This zwitterionic amino acid, specifically the L-form, is the enantiomer that is naturally occurring and biologically active in humans and many other organisms. The presence of a monohydrate form indicates that each molecule of asparagine is associated with one water molecule, which can influence its solubility, stability, and reactivity. As a result of its significance in biological processes and industrial applications, L(+)-Asparagine monohydrate has garnered considerable attention in recent years.
The compound is primarily utilized as a building block in the synthesis of peptides and proteins due to its role as a non-essential amino acid. It is also employed in various research applications, including enzyme kinetics studies, metabolic pathways analysis, and as a supplement in cell culture media. The hydrate form enhances the compound's solubility in aqueous solutions, making it particularly useful for laboratory experiments and large-scale industrial processes.
In recent years, L(+)-Asparagine monohydrate has been the subject of numerous studies aimed at exploring its potential therapeutic applications. One of the most promising areas of research is its role in cancer therapy. Studies have shown that asparagine deprivation can selectively starve tumor cells, which rely heavily on this amino acid for growth and proliferation. This concept has led to the development of novel therapeutic strategies that target asparaginase enzymes, which catalyze the hydrolysis of asparagine into aspartic acid and ammonia.
Moreover, L(+)-Asparagine monohydrate has been investigated for its potential benefits in the field of regenerative medicine. Research indicates that it can support tissue repair and wound healing by providing essential nutrients to cells and promoting the synthesis of extracellular matrix components. This has opened up new avenues for developing advanced wound care products and tissue engineering scaffolds.
The food industry also benefits from L(+)-Asparagine monohydrate due to its role as a flavor enhancer and nutrient supplement. It is commonly added to infant formulas, sports supplements, and other specialized dietary products to improve nutritional value and taste profile. Its stability under various processing conditions makes it an ideal candidate for use in food formulations where consistency and purity are paramount.
Recent advancements in analytical chemistry have further highlighted the importance of L(+)-Asparagine monohydrate in quality control processes. High-performance liquid chromatography (HPLC) and mass spectrometry (MS) techniques have enabled researchers to accurately determine the purity and concentration of this compound in complex mixtures. These methods are crucial for ensuring that pharmaceutical products meet stringent regulatory standards before they reach the market.
The synthesis of L(+)-Asparagine monohydrate has also seen significant improvements over the years. Traditional methods often relied on enzymatic hydrolysis or chemical synthesis from precursor molecules like aspartic acid or mesaconic acid. However, newer approaches have focused on more sustainable and cost-effective production techniques. For instance, fermentation processes using genetically modified microorganisms have been developed to produce high-purity L(+)-Asparagine monohydrate on an industrial scale.
The impact of L(+)-Asparagine monohydrate extends beyond its direct applications into broader scientific fields such as bioinformatics and systems biology. By understanding how this amino acid interacts with other molecules within cellular environments, researchers can gain insights into complex biological pathways and disease mechanisms. This knowledge is invaluable for developing targeted therapies and personalized medicine approaches.
In conclusion, L(+)-Asparagine monohydrate (CAS No. 5794-13-8) is a multifaceted compound with diverse applications across multiple industries. Its role in pharmaceuticals, biotechnology, food science, and research underscores its importance as a key component in modern science and industry. As research continues to uncover new uses for this compound, its significance is likely to grow even further.
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