Cas no 328-42-7 (Oxaloacetic Acid)
Oxaloacetic Acid Chemical and Physical Properties
Names and Identifiers
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- 2-Oxosuccinic acid
- Oxosuccinic acid
- Oxalacetic acid 2-Oxosuccinic
- Oxaloacetic acid
- Oxalacetic acid
- Oxobutanedioic acid
- 2-OXOSUCCINIC
- 2-Oxosuccinic acid,Ketosuccinic acid,Oxalacetic acid
- ketosuccinic acid
- OAA
- oxalacetic
- OXALEACETIC ACID
- OXLACETIC ACID
- keto-oxaloacetate
- BDBM23230
- HY-W010382
- Butanedioic acid, oxo-
- SCHEMBL8464
- Oxaloacetic acid, Hybri-Max(TM), powder, suitable for hybridoma
- s6112
- DTXSID8021646
- Butanedioic acid, oxo- (9CI)
- AS-17361
- 4cts
- alpha-Ketosuccinate
- 328-42-7
- 2-Ketosuccinate
- H12016
- Oxalacetic acid (8CI)
- alpha-Ketosuccinic acid
- Oxaloethanoic acid
- Ketosuccinate
- Z271128590
- Tox21_201215
- NS00015158
- CHEBI:30744
- C00036
- NSC-77688
- a-Ketosuccinate
- GTPL5236
- NCGC00258767-01
- Oxaloacetic acid, powder, BioReagent, suitable for cell culture, suitable for insect cell culture, >=97% (HPLC)
- 2-Oxobutanedioic acid
- AKOS000121850
- BCP16299
- OXOSUCCINIC ACID [INCI]
- 3-carboxy-3-oxopropanoic acid
- CHEMBL1794791
- FT-0631962
- OXALACETIC ACID TRANS-(Z)-ENOL FORM [MI]
- Oxaloethanoate
- Anhydrous enol-oxaloacetate
- Oxaloacetic acid, >=97% (HPLC)
- EINECS 206-329-8
- OXALACETIC ACID [MI]
- F15D7D2F-5E37-4B87-A8D2-824D5097A4DE
- Oxalacetic acetic
- a-Ketosuccinic acid
- NSC 77688
- A875503
- UNII-2F399MM81J
- Butanedioic acid, 2-oxo-
- 2-oxobutanedioate
- EN300-28603
- Bioepg
- 2-Oxosuccinate
- CAS-328-42-7
- NCGC00248960-01
- 7619-04-7
- J-650320
- 2F399MM81J
- J-650383
- LMFA01170120
- 2-Ketosuccinic acid
- DTXCID901646
- NSC77688
- O0072
- CS-W011098
- O-5000
- OXALACETIC ACID [WHO-DD]
- oxaloacetate
- Q408658
- 2-oxo-butanedioic acid
- MFCD00002592
- oxosuccinate
- oxaloacetate dianion
- oxobutanedioic acid, ion(2-)
- oxalacetate
- oxobutanedioate
- keto-succinic acid
- DB-228237
- OxalaceticAcid
- BRD-K61279411-001-02-0
- SY010263
- STL168038
- DB-048279
- 206-329-8
- 2 Ketosuccinic Acid
- 2ketosuccinic acid
- Butanedioic acid, 2oxo
- OXALACETIC ACID TRANS-(Z)-ENOL FORM
- FO12113
- Acid, Oxalacetic
- 2Oxobutanedioic acid
- Acid, Oxaloacetic
- Butanedioic acid, oxo
- 2 oxo Butanedioic Acid
- Oxaloacetic Acid
-
- MDL: MFCD00002592
- Inchi: 1S/C4H4O5/c5-2(4(8)9)1-3(6)7/h1H2,(H,6,7)(H,8,9)
- InChI Key: KHPXUQMNIQBQEV-UHFFFAOYSA-N
- SMILES: OC(CC(C(=O)O)=O)=O
- BRN: 1705475
Computed Properties
- Exact Mass: 132.00600
- Monoisotopic Mass: 132.00587322g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 9
- Rotatable Bond Count: 3
- Complexity: 158
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 91.7?2
- Surface Charge: 0
- Tautomer Count: 3
- XLogP3: -0.6
Experimental Properties
- Color/Form: Unstable liquid, its methyl ester is colorless crystal.
- Density: 1.3067 (rough estimate)
- Melting Point: 161 oC
- Boiling Point: 163.94°C (rough estimate)
- Flash Point: 88°C
- Refractive Index: 1.4000 (estimate)
- Solubility: H2O: 100?mg/mL
- Water Partition Coefficient: dissolution
- Stability/Shelf Life: Stable. Incompatible with strong oxidizing agents. Keep refrigerated.
- PSA: 91.67000
- LogP: -0.88520
- Solubility: Not available
- Merck: 6909
- pka: 2.22(at 25℃)
- Sensitiveness: Sensitive to heat
Oxaloacetic Acid Security Information
-
Symbol:
- Prompt:dangerous
- Signal Word:Danger
- Hazard Statement: H314
- Warning Statement: P280,P305+P351+P338,P310
- Hazardous Material transportation number:UN 3261 8/PG 2
- WGK Germany:3
- Hazard Category Code: 34
- Safety Instruction: S26-S36/37/39-S45
-
Hazardous Material Identification:
- HazardClass:8
- PackingGroup:II
- TSCA:Yes
- Storage Condition:0-10°C
- Packing Group:II
- Hazard Level:8
- Safety Term:8
- Packing Group:II
- Risk Phrases:R34
Oxaloacetic Acid Customs Data
- HS CODE:2918300090
- Customs Data:
China Customs Code:
2918300090Overview:
2918300090 Other aldehydes or ketones without other oxy carboxylic acids(Including anhydrides\Acyl halide\Peroxides, peroxyacids and derivatives of this tax number). VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:6.5% general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Summary:
2918300090 other carboxylic acids with aldehyde or ketone function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives.Supervision conditions:None.VAT:17.0%.Tax rebate rate:9.0%.MFN tariff:6.5%.General tariff:30.0%
Oxaloacetic Acid Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | O815182-5g |
Oxalacetic acid |
328-42-7 | 98% | 5g |
446.00 | 2021-05-17 | |
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | O0072-25G |
Oxalacetic Acid |
328-42-7 | >97.0%(T) | 25g |
¥1190.00 | 2024-04-15 | |
| TRC | O845030-1g |
Oxaloacetic Acid |
328-42-7 | 1g |
$ 58.00 | 2023-09-06 | ||
| TRC | O845030-5g |
Oxaloacetic Acid |
328-42-7 | 5g |
$ 81.00 | 2023-09-06 | ||
| TRC | O845030-10g |
Oxaloacetic Acid |
328-42-7 | 10g |
$ 115.00 | 2023-09-06 | ||
| TRC | O845030-50g |
Oxaloacetic Acid |
328-42-7 | 50g |
$460.00 | 2023-05-17 | ||
| SHANG HAI TAO SHU Biotechnology Co., Ltd. | T4862-100 mg |
Oxaloacetic acid |
328-42-7 | 99.25% | 100MG |
¥485.00 | 2022-04-26 | |
| SHANG HAI TAO SHU Biotechnology Co., Ltd. | T4862-1 mL * 10 mM (in DMSO) |
Oxaloacetic acid |
328-42-7 | 99.25% | 1 mL * 10 mM (in DMSO) |
¥530.00 | 2022-04-26 | |
| ChemScence | CS-W011098-100mg |
Oxaloacetic acid |
328-42-7 | ≥98.0% | 100mg |
$50.0 | 2021-09-02 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | O74861-1g |
2-Oxosuccinic acid |
328-42-7 | 97% | 1g |
¥118.0 | 2024-07-19 |
Oxaloacetic Acid Suppliers
Oxaloacetic Acid Related Literature
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Ya-Ping Xue,Cheng-Hao Cao,Yu-Guo Zheng Chem. Soc. Rev. 2018 47 1516
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Paola D'Arrigo,Chiara Allegretti,Andrea Fiorati,Luciano Piubelli,Elena Rosini,Davide Tessaro,Mattia Valentino,Loredano Pollegioni Catal. Sci. Technol. 2015 5 1106
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Yutaka Amao,Shusaku Ikeyama,Takayuki Katagiri,Kohei Fujita Faraday Discuss. 2017 198 73
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Václav Pokorny,Petr Tou?,Vojtěch ?tejfa,Květoslav R??i?ka,Jan Rohlí?ek,Ji?í Czernek,Ji?í Brus,Ctirad ?ervinka Phys. Chem. Chem. Phys. 2022 24 25904
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Vincent Artero,Leif Hammarstr?m,Fengtao Fan,Dong Ryeol Whang,Jose Martinez,Anthony Harriman,Takumi Noguchi,Joshua Karlsson,Peter Summers,Shigeru Itoh,Richard Cogdell,Alexander Kibler,Johannes Ehrmaier,Hitoshi Tamiaki,Etsuko Fujita,Seigo Shima,Shunya Yoshino,Haruo Inoue,Michael Wasielewski,Thomas Corry,Devens Gust,Flavia Cassiola,Hitoshi Ishida,Katsuhiko Takagi,Sang Ook Kang,Can Li,Licheng Sun,Hyunwoong Park,Hideki Hashimoto,Yutaka Amao,Eun Jin Son,Nobuo Kamiya,Jian-Ren Shen,Kizashi Yamaguchi Faraday Discuss. 2017 198 147
Additional information on Oxaloacetic Acid
Oxaloacetic Acid: A Comprehensive Overview
Oxaloacetic acid, also known by its CAS number 328-42-7, is a naturally occurring organic compound that plays a significant role in various biochemical pathways. It is a dicarboxylic acid with the molecular formula C4H6O5 and is commonly found in plants, particularly in the leaves, where it serves as an intermediate in the tricarboxylic acid (TCA) cycle and the glyoxylate cycle. Oxaloacetic acid is also involved in gluconeogenesis, a metabolic pathway that generates glucose from non-carbohydrate precursors.
Recent studies have highlighted the importance of oxaloacetic acid in cellular metabolism and its potential therapeutic applications. For instance, research has shown that oxaloacetic acid can act as a precursor for the synthesis of other essential biomolecules, such as citrate and malate, which are critical for energy production in cells. Furthermore, oxaloacetic acid has been implicated in the regulation of oxidative stress and inflammation, making it a promising candidate for the development of novel anti-inflammatory and antioxidant therapies.
In terms of industrial applications, oxaloacetic acid is widely used as a precursor in the synthesis of various organic compounds, including amino acids and pharmaceuticals. Its ability to participate in multiple metabolic pathways makes it a valuable intermediate in biotechnology and chemical manufacturing. Recent advancements in metabolic engineering have enabled the efficient production of oxaloacetic acid through microbial fermentation, which has significantly reduced production costs and improved scalability.
The structural properties of oxaloacetic acid also contribute to its versatility in biochemical systems. Its two carboxylic acid groups allow it to participate in various enzymatic reactions, including decarboxylation and transamination. These reactions are essential for maintaining cellular homeostasis and ensuring proper energy metabolism. Recent research has focused on understanding the role of oxaloacetic acid in mitochondrial function and its potential implications for neurodegenerative diseases such as Alzheimer's disease.
Moreover, oxaloacetic acid has been shown to exhibit anti-diabetic properties by enhancing insulin sensitivity and improving glucose metabolism. Studies have demonstrated that supplementation with oxaloacetic acid can reduce blood glucose levels and improve lipid profiles in diabetic animal models. These findings suggest that oxaloacetic acid could be a potential therapeutic agent for managing metabolic disorders associated with insulin resistance.
In conclusion, oxaloacetic acid (CAS No. 328-42-7) is a multifunctional compound with significant roles in cellular metabolism, energy production, and disease prevention. Its versatility as a biochemical intermediate and its emerging therapeutic applications make it an area of active research interest. As our understanding of its molecular mechanisms continues to grow, oxaloacetic acid is poised to play an even more critical role in both basic science and applied medicine.
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