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Ammonium L-tartrate | CAS:3164-29-2
Ammonium L-tartrate
  • Name:Ammonium L-tartrate
  • CAS:3164-29-2
  • Synonyms:2,3-Dihydroxybutanedioic acid diammonium salt; L-Tartaric acid diammonium salt
  • Molecular Formula:C4H12N2O6
  • Molecular Weight:184.15
  • EINESC:221-618-9

Description

Properties

Specific optical rotation 32.4 º (c=1.84, H2O)
Water Solubility 63 g/L (15 ºC)
Density 1.6

Safety

SDS/MSDS S24/25

SDS

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Peer-Reviewed Papers
2-Butyl-2-tert-butyl-5,5-diethylpyrrolidine-1-oxyls: Synthesis and Properties.Irina F Zhurko et al.Molecules (Basel, Switzerland), 25(4) (2020-02-23) Highly selective asymmetric acetate aldol reactions of an N-acetyl thiazolidinethione reagent.Yingchao Zhang et al.Organic letters, 6(1), 23-25 (2004-01-03) Enzyme-assisted preparation of D-tert.-leucine.K Laumen et al.Bioscience, biotechnology, and biochemistry, 65(9), 1977-1980 (2001-10-26) Effect of organic cosolvent on kinetic resolution of tert-leucine by penicillin G acylase from Kluyvera citrophila.Shu-Lai Liu et al.Bioprocess and biosystems engineering, 28(5), 285-289 (2005-10-26) Stabilizing and destabilizing effects of placing beta-branched amino acids in protein alpha-helices.V W Cornish et al.Biochemistry, 33(40), 12022-12031 (1994-10-11) The tert-butyl group in chemistry and biology.Philippe Bisel et al.Organic & biomolecular chemistry, 6(15), 2655-2665 (2008-07-18) Preferred conformations of peptides containing tert-leucine, a sterically demanding, lipophilic alpha-amino acid with a quaternary side-chain Cbeta atom.Fernando Formaggio et al.Chemistry (Weinheim an der Bergstrasse, Germany), 11(8), 2395-2404 (2005-01-26) Scaleable catalytic asymmetric Strecker syntheses of unnatural alpha-amino acids.Stephan J Zuend et al.Nature, 461(7266), 968-970 (2009-10-16) An efficient and selective enzymatic oxidation system for the synthesis of enantiomerically pure D-tert-leucine.Werner Hummel et al.Organic letters, 5(20), 3649-3650 (2003-09-26) Asymmetric construction of spirocyclohexanonerhodanines catalyzed by simple diamine derived from chiral tert-leucine.Wenbin Wu et al.Chemical communications (Cambridge, England), 48(73), 9180-9182 (2012-08-07)
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