(+)-3-Bromocamphor-8-sulfonic Acid Ammonium Salt TCI B1125

Chemical Identity

CAS No.: 14575-84-9
PubChem: CID 44630124·SID 87564068
Formula: C10H18BrNO4S
Molecular weight: 328.23 g/mol
Purity: >98.0%(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: azanium [(1S,3S,4R,7R)-3-bromo-1,7-dimethyl-2-oxo-7-bicyclo[2.2.1]heptanyl]methanesulfonate
SMILES: C[C@]12CC[C@H]([C@@]1(C)CS(=O)(=O)[O-])[C@@H](C2=O)Br.[NH4+]
InChIKey: GFBVBBRNPGPROZ-ZVGXWIELSA-N

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(+)-3-Bromocamphor-8-sulfonic Acid Ammonium Salt is a chiral compound widely used in asymmetric synthesis to construct molecules with optical activity. This material plays a crucial role in laboratory settings where precise control over stereochemistry is essential. It is commonly employed in chemical reactions that require the selective formation of specific stereoisomers, making it a vital component in the development of complex organic structures. Its chiral nature allows it to act as a chiral auxiliary or catalyst, enabling the synthesis of compounds with defined stereochemistry.

The compound’s unique properties, including its chiral structure and reactivity, make it a preferred choice for researchers working in asymmetric synthesis. Its ability to influence reaction pathways and control the stereochemical outcome of chemical transformations sets it apart from other reagents. This makes it particularly useful in applications where the spatial arrangement of atoms is critical, such as in pharmaceutical and industrial chemistry. Its reliability and consistent performance in controlled environments further enhance its appeal in laboratory research.

In Indonesian laboratories, this compound is frequently used by chemists, pharmacologists, and advanced students conducting research on asymmetric synthesis. It is especially relevant in the development of new compounds with applications in medicine, pharmaceuticals, and chemical industries. Its role in enabling precise molecular construction supports innovation and discovery in various scientific fields.

TCI brochures (PDF)

Terpenes 2025-09-22 · p. 5
Chiral Building Blocks 2025-04-14 · p. 15

Related TCI products

Asymmetric synthesis of optically active compounds due to its chiral structure and ability to control stereochemical outcomes.
Development of pharmaceuticals requiring specific stereoisomers for therapeutic efficacy and selectivity.
Organic chemistry research focused on creating complex molecular frameworks with defined stereochemistry.
Industrial chemical synthesis where precise stereocontrol is necessary for product quality and functionality.
Academic research in chiral building blocks for teaching and experimental studies in asymmetric catalysis.

Brand	TCI
CAS number	14575-84-9
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in standard laboratory quantities as per supplier specifications
Physical form	Solid powder (as per typical chemical compound form)
Storage	Store in a cool, dry place away from moisture and direct sunlight

This compound should be stored in a cool, dry environment to maintain its chemical integrity and prevent degradation. It is recommended to use airtight containers to protect it from moisture and humidity, which can affect its stability. Due to its chiral nature, it is important to handle it with care to avoid contamination or unintended stereochemical changes. Proper labeling and storage conditions ensure that it remains effective for its intended applications. Always follow standard laboratory safety protocols when handling and storing chiral compounds to maintain a safe and controlled environment.

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