L-Aspartic acid di-tert-butyl ester hydrochloride
Need Assistance?
  • US & Canada:
    +
  • UK: +

L-Aspartic acid di-tert-butyl ester hydrochloride

* Please kindly note that our products are not to be used for therapeutic purposes and cannot be sold to patients.

Category
β−Amino Acids
Catalog number
BAT-004225
CAS number
1791-13-5
Molecular Formula
C12H23NO4·HCl
Molecular Weight
281.78
L-Aspartic acid di-tert-butyl ester hydrochloride
Size Price Stock Quantity
500 g $599 In stock
1 kg $999 In stock
IUPAC Name
ditert-butyl (2S)-2-aminobutanedioate;hydrochloride
Synonyms
L-Asp(OtBu)-OtBu HCl; L-Aspartic acid di-tert-butyl ester hydrochloride; H-Asp(OtBu)-OtBu HCl; aspartic acid di-t-butyl ester hydrochloride; (S)-Di-tert-butyl 2-aminosuccinate hydrochloride; H-Asp(OtBu)-OtBu HCl
Appearance
White powder
Purity
≥ 99% (HPLC)
Melting Point
130-150 °C
Boiling Point
339.8 °C at 760 mmHg
Storage
Store at 2-8 °C
InChI
InChI=1S/C12H23NO4.ClH/c1-11(2,3)16-9(14)7-8(13)10(15)17-12(4,5)6;/h8H,7,13H2,1-6H3;1H/t8-;/m0./s1
InChI Key
GVLZIMQSYQDAHB-QRPNPIFTSA-N
Canonical SMILES
CC(C)(C)OC(=O)CC(C(=O)OC(C)(C)C)N.Cl

L-Aspartic acid di-tert-butyl ester hydrochloride, a chemical compound widely utilized in biochemical and pharmaceutical research, boasts diverse applications. Here are four key applications:

Peptide Synthesis: An indispensable player in the realm of peptide synthesis, L-Aspartic acid di-tert-butyl ester hydrochloride serves as a key intermediate in crafting peptides and proteins. Its protective groups function as guardians, warding off undesired reactions during peptide bond formation, thereby elevating the efficiency of the synthesis process. This meticulous approach culminates in the production of peptides of exceptional purity, catering to both research and therapeutic pursuits.

Drug Development: Positioned at the forefront of pharmaceutical exploration, this compound holds significant value in shaping the landscape of drug development. Acting as a fundamental building block, it aids researchers in synthesizing amino acid derivatives infused with promising pharmacological activities. Scientists leverage its capabilities to unearth novel therapeutic agents, fine-tuning compounds for optimal efficacy and safety.

Metabolic Studies: Delving into the intricate realm of metabolic research, L-Aspartic acid di-tert-butyl ester hydrochloride emerges as a pivotal tool for dissecting amino acid metabolism pathways. Infusing it into experimental frameworks, scientists navigate metabolic processes, scrutinizing the impact of diverse substances on aspartate metabolism. This deep dive allows for a comprehensive understanding of metabolic disorders and for the formulation of targeted metabolic intervention.

Organic Synthesis: Within the realm of organic chemistry, L-Aspartic acid di-tert-butyl ester hydrochloride assumes a pivotal role as a versatile reagent for a myriad of synthetic transformations.

Online Inquiry
Verification code
Inquiry Basket