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D-Alanine H-D-Abu-OH D-2-Aminopropionic acid
In addition to our core competence in the standard unit operations of organic chemical synthesis, we offer specialised reaction technology, including innovative organometallic synthesis, catalytic transfer hydrogenation and the various operations required for synthesis of chiral compounds.
D-Alanine
CAS RN: 338-69-2
H-D-Ala-OH
(2R)-2-aminopropanoic acid
(R)-Alanine
Solubility in water | Colorless & clear (c=5) |
Specific rotation [α]D20 | -13.7°~-15.0°(c= 4, 6M-HCl) |
Loss on drying | Not more than 0.3% |
Residue on ignition (as sulfate) | Not more than 0.1% |
Chloride (Cl) | Not more than 0.02% |
Sulfate (SO4) | Not more than 0.03% |
Heavy metals (as Pb) | Not more than 10ppm |
Iron (Fe) | Not more than 10ppm |
Ammonium (NH4) | Not more than 0.02% |
Arsenic (As2O3) | Not more than 1ppm |
Other amino acids | Not detected by T.L.C.(The spotted amount, 10μg) |
Assay | 98.5%~101.0% |
L-Isomer | Not more than 0.5% |
Scope of services: compound custom synthesis, chemical custom synthesis, peptide custom synthesis, protein synthesis, pharmaceutical intermediate custom synthesis, generic synthesis, chemical custom synthesis CRO, etc.With strong technical accumulation and innovative research and development capabilities, he is good at various types of chemical reactions such as hydrogenation, nitration, Suzuki coupling, cyanation, diazotization, bromination, wittig reaction, Grignard reaction, redox reaction and ultra-low temperature reaction.The company's production base is equipped with enamel reactors from 50L to 5000L, stainless steel ultra-low temperature reactors and conventional separation and drying equipment.By following our guiding principles of Samples, Quotes, Literature, and Innovation, we are able to make continual process improvements for customers.In addition to our core competence in the standard unit operations of organic chemical synthesis, we offer specialised reaction technology, including innovative organometallic synthesis, catalytic transfer hydrogenation and the various operations required for synthesis of chiral compounds.
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