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TCI

CAS 551-16-6

6-Aminopenicillanic Acid TCI A0800

6-Aminopenicillanic Acid TCI A0800

Chemical Identity

CAS No.
551-16-6
PubChem
CID 11082·SID 87562327
Formula
C8H12N2O3S
Molecular weight
216.26 g/mol
Purity
>98.0%(HPLC)
Reference databases
ChEBI·ChemSpider·ECHA·Wikipedia
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(2S,5R,6R)-6-amino-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
SMILES
CC1([C@@H](N2[C@H](S1)[C@@H](C2=O)N)C(=O)O)C
InChIKey
NGHVIOIJCVXTGV-ALEPSDHESA-N
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6-Aminopenicillanic Acid (6-APA) is a key chemical compound widely used in laboratory settings for the synthesis of beta-lactam antibiotics, including penicillin and cephalosporins. As a chiral building block, it plays a crucial role in asymmetric synthesis, enabling the creation of molecules with specific spatial configurations. This property makes it essential for developing pharmaceutical compounds with precise stereochemistry, which is vital for their biological activity and efficacy. Its significance extends to organic chemistry and pharmacology research, where it is employed to explore new drug development pathways.

The chemical stability of 6-APA under controlled conditions, combined with its ability to undergo highly specific chemical reactions, makes it a preferred choice for researchers. Its complex molecular structure allows for a wide range of synthetic transformations, supporting the design of bioactive compounds. Additionally, its sensitivity to high temperatures and air exposure requires careful handling, which further underscores its importance in controlled laboratory environments. These characteristics make it a versatile and reliable reagent for advanced chemical synthesis.

In Indonesian laboratories, 6-APA is commonly used in research focused on antibiotic development and pharmacological compound synthesis. It is a fundamental component in studies aimed at creating more effective and safer medications. Its role in supporting scientific innovation in the pharmaceutical sector highlights its significance in both academic and industrial research settings.

TCI brochures (PDF)

  • Asymmetric synthesis applications benefit from 6-APA's chiral structure, enabling precise stereochemical control in drug development.
  • Pharmaceutical research relies on 6-APA for the synthesis of beta-lactam antibiotics, contributing to the creation of new therapeutic agents.
  • Organic chemistry experiments utilize 6-APA due to its reactivity and ability to participate in complex molecular transformations.
  • Pharmacological studies use 6-APA to investigate the effects of stereochemistry on drug efficacy and biological activity.
  • Antibiotic development programs incorporate 6-APA as a core building block in the synthesis of penicillin and cephalosporin derivatives.

Brand TCI
CAS number 551-16-6
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes —
Physical form —
Storage Store in a cool, dry place away from light and moisture

6-Aminopenicillanic Acid should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air, which can degrade the compound. Due to its sensitivity to high temperatures, it should be kept at controlled room temperature. In laboratory settings, it is important to handle the compound with care, using appropriate personal protective equipment to ensure safety. Proper labeling and storage conditions are essential to prevent contamination and ensure the integrity of the material for research purposes.

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