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Thermo Scientific Chemicals
(±)-Isoborneol, 95%
CAS: 124-76-5 | C10H18O | 154.253 g/mol
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Catalog number B20632.36
also known as B20632-36
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Quantity:
500 g
Chemical Identifiers
CAS124-76-5
IUPAC Name(1R,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
Molecular FormulaC10H18O
InChI KeyDTGKSKDOIYIVQL-XKSSXDPKSA-N
SMILESCC1(C)[C@H]2CC[C@@]1(C)[C@H](O)C2
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White
FormCrystals or powder or crystalline powder or lumps
Identification (FTIR)Conforms
Assay (GC)≥94.0%
Used as a synthetic flavor, as a moth repellent, cold sore topical medication, muscle liniment, and steam-inhaled cough suppressant. It is also used in Used in perfumes.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Used as a synthetic flavor, as a moth repellent, cold sore topical medication, muscle liniment, and steam-inhaled cough suppressant. It is also used in Used in perfumes.
Solubility
Insoluble in water. Soluble in dipropylene glycol, ethyl alcohol (1gm. in 2ml. 70% alcohol).
Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
Used as a synthetic flavor, as a moth repellent, cold sore topical medication, muscle liniment, and steam-inhaled cough suppressant. It is also used in Used in perfumes.
Solubility
Insoluble in water. Soluble in dipropylene glycol, ethyl alcohol (1gm. in 2ml. 70% alcohol).
Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
RUO – Research Use Only
General References:
- Maria Armaka, et al. Antiviral properties of isoborneol, a potent inhibitor of herpes simplex virus type 1.Antiviral Res.1999,43(2), 79-92.
- Wolfgang Oppolzer, et al. High asymmetric induction in diels-alder additions of cyclopentadiene to acrylates derived from isoborneol.Tetrahedron Lett.1982,23(46), 4781-4784.