(+/-)-Camphor TCI C0011

Chemical Identity

CAS No.: 76-22-2
PubChem: CID 2537·SID 87565222
Formula: C10H16O
Molecular weight: 152.24 g/mol
Purity: >95.0%(GC)
Reference databases: ChEBI·ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
SMILES: CC1(C2CCC1(C(=O)C2)C)C
InChIKey: DSSYKIVIOFKYAU-UHFFFAOYSA-N
MDL: MDL00074738

Rp 477.750,00

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Berat 25g 500g

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TCI C0011 (+/-)-Camphor, CAS 76-22-2, is the racemic form of the well-known bicyclic terpenoid ketone. It is intended for applications where optical purity is not required, serving as an economical non-heterocyclic building block for general synthetic work. The reactive carbonyl group readily undergoes reduction, oximation, and condensation reactions, while its ready sublimation makes it a classic teaching material. AMI Scientific provides this TCI product in 25 g and 500 g pack sizes for research and teaching laboratories alike.

TCI brochures (PDF)

Terpenes 2025-09-22 · p. 5
Phytochemicals 2025-12-17 · p. 6
Reagents for Biological Research 2025-03-11 · p. 53

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Chan et al. (2009). Status epilepticus after topical application of a solution containing camphor. Emergency Medicine Journal doi:10.1136/emj.2008.063198
YE et al. (1991). ChemInform Abstract: Selective Anodic Oxidation of Camphor.. ChemInform doi:10.1002/chin.199142265
STINSON (1998). Chiral camphor carries acetate in asymmetric condensation. Chemical & Engineering News Archive doi:10.1021/cen-v076n005.p029

References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.