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Chemical formula: C 3 H 7 N O 2 Molar mass: 89.1 g·mol −1 Systematic name: (S)-2-aminopropanoic acid Abbreviations: A, Ala Synonyms: 2-aminopropanoic acid {α/2}-aminopropionic acid AIDS{-}071780 HSDB 1801 NSC 206315
Alanine is an aliphatic amino acid, because the side-chain connected to the α-carbon atom is a methyl group (-CH 3). Alanine is the simplest α-amino acid after glycine. The methyl side-chain of alanine is non-reactive and is therefore hardly ever directly involved in protein function. [12]
An obvious synthesis route to α-alaninediacetic acid is from racemic α-DL-alanine, which provides racemic α-ADA by double cyanomethylation with methanal and hydrogen cyanide, hydrolysis of the intermediately formed diacetonitrile to the trisodium salt and subsequent acidification with mineral acids in a 97.4% overall yield. [4]
The molar mass is defined as the mass of a given substance divided by the amount of the substance, and is expressed in grams per mol (g/mol). That makes the molar mass an average of many particles or molecules (potentially containing different isotopes), and the molecular mass the mass of one specific particle or molecule. The molar mass is ...
molar mass [note 1] amphetamine base [note 2] amphetamine base in equal doses doses with equal base content [note 3] (g/mol) (percent) (30 mg dose) total base total dextro- levo- dextro- levo- dextroamphetamine sulfate [2] [3] (C 9 H 13 N) 2 •H 2 SO 4
Aminopropionic acid (C3H7NO2, molar mass 89.093 g/mol) may refer to: 2-Aminopropionic acid, or alanine; 3-Aminopropionic acid, or β-alanine
This improper name persists, especially in elementary textbooks. In biology, the unit "%" is sometimes (incorrectly) used to denote mass concentration, also called mass/volume percentage. A solution with 1 g of solute dissolved in a final volume of 100 mL of solution would be labeled as "1%" or "1% m/v" (mass/volume). This is incorrect because ...
β-Alanine (beta-alanine) is a naturally occurring beta amino acid, which is an amino acid in which the amino group is attached to the β-carbon (i.e. the carbon two carbon atoms away from the carboxylate group) instead of the more usual α-carbon for alanine (α-alanine). The IUPAC name for β-alanine is 3-aminopropanoic acid.