Name | Succinic acid-2,3-13C2 |
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Synonyms |
Butanedioic acid-2,3-13C2
<2,3-13C2>Bernsteinsaeure 1,4-butanedioic acid-2,3-13C2 MFCD00145336 butanedioic-2,3-13C2 acid <2,3-13C2>succinic acid Succinic Acid (2,3-13C2, 99%) |
Description | Succinic acid-13C2 is the 13C labeled Succinic acid[1]. Succinic acid is a potent and orally active anxiolytic agent. Succinic acid is an intermediate product of the tricarboxylic acid cycle. Succinic acid can be used as a precursor of many industrially important chemicals in food, chemical and pharmaceutical industries[2][3]. |
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Related Catalog | |
In Vitro | Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1]. |
References |
[4]. Si Wei Chen, Anxiolytic-like effect of succinic acid in mice. Life Sci. 2003 Nov 773(25):3257-64. |
Density | 1.408g/cm3 |
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Boiling Point | 235ºC |
Melting Point | 187-190ºC(lit.) |
Molecular Formula | C4H6O4 |
Molecular Weight | 120.07300 |
Exact Mass | 120.03300 |
PSA | 74.60000 |
Index of Refraction | 1.477 |
Symbol |
GHS05, GHS07 |
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Signal Word | Danger |
Hazard Statements | H315-H318-H335 |
Precautionary Statements | P261-P280-P305 + P351 + P338 |
Hazard Codes | Xi |
Risk Phrases | 36/37/38-41 |
Safety Phrases | 26-36 |
RIDADR | NONH for all modes of transport |
~64% 61128-08-3 |
Literature: Cane; Liang; Hasler Journal of the American Chemical Society, 1982 , vol. 104, # 25 p. 7274 - 7281 |
~% 61128-08-3 |
Literature: Kushner; Weinhouse Journal of the American Chemical Society, 1949 , vol. 71, p. 3558 |
~% 61128-08-3 |
Literature: Ashworth, Doreen M.; Robinson, John A.; Turner, David L. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1988 , p. 1719 - 1728 |
~% 61128-08-3 |
Literature: Franke, Wilfried; Schwarz, Helmut; Thies, Helga; Chandrasekhar, Jayaraman; Raque' Schleyer, Paul von; et al. Chemische Berichte, 1981 , vol. 114, # 8 p. 2808 - 2824 |
Precursor 4 | |
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DownStream 0 |