Name | N-acetyl-DL-aspartic acid |
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Synonyms |
2-Acetamidosuccinic acid
N-Acetyl aspartic acid MFCD00066022 Aspartic acid, N-acetyl- N-Acetyl-DL-aspartic acid 2-acetamidobutanedioic acid N-Acetyl-DL-aspartic EINECS 219-827-5 AC-DL-ASPARTIC ACID acetylaspartic acid N-Acetylaspartic acid N-ACETYL-DL-ASPARAGINE N-acetyl-aspartate AC-DL-ASN-OH ACETYL-DL-ASPARAGINE AC-DL-ASP-OH |
Description | 2-Acetamidosuccinic acid is an aspartic acid derivative[1]. |
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Related Catalog | |
In Vitro | Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. |
References |
Density | 1.4±0.1 g/cm3 |
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Boiling Point | 425.3±35.0 °C at 760 mmHg |
Molecular Formula | C6H9NO5 |
Molecular Weight | 175.139 |
Flash Point | 211.0±25.9 °C |
Exact Mass | 175.048065 |
PSA | 103.70000 |
LogP | -1.05 |
Vapour Pressure | 0.0±2.2 mmHg at 25°C |
Index of Refraction | 1.506 |
Storage condition | 2-8°C |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2924199090 |
~% 2545-40-6 |
Literature: Biochemical Journal, , vol. 27, p. 338,343 Journal of the Chemical Society, , p. 453,456 Biochemical Journal, , vol. 37, p. 82 |
~% 2545-40-6 |
Literature: Biochemical Journal, , vol. 27, p. 338,343 |
~% 2545-40-6 |
Literature: Journal of Biochemistry (Tokyo, Japan), , vol. 45, p. 745,746 Australian Journal of Scientific Research, Series A: Physical Sciences, , vol. 5, p. 728,732 |
Precursor 4 | |
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DownStream 6 | |
HS Code | 2924199090 |
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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% |