An acetate form of borneol
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(±)-Bornyl Acetate

Item No. 29617

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
(1R,2S,4R)-rel-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-ol, 2-acetate
CAS Number
76-49-3
Molecular Formula
C12H20O2
Formula Weight
196.3
Purity
≥95%
Formulation (Request formulation change)
An oil
Solubility(Learn about Variance in Solubility)
DMF: 25mg/mLDMF:PBS (pH 7.2) (1:3): 0.25mg/mLDMSO: 2mg/mLEthanol: 15mg/mL
SMILES
C[C@@]1(C2(C)C)CC[C@H]2C[C@H]1OC(C)=O
InChi Code
InChI=1S/C12H20O2/c1-8(13)14-10-7-9-5-6-12(10,4)11(9,2)3/h9-10H,5-7H2,1-4H3/t9-,10+,12+/m0/s1
InChi Key
KGEKLUUHTZCSIP-HOSYDEDBSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    10 g

    $103

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    25 g

    $240

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    50 g

    $454

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    Product Description

    (±)-Bornyl acetate is a racemic mixture of the acetate form of the monoterpene alcohol borneol (Item Nos. 23467 | 23468) that has been found in P. silvestris.1,2 (±)-Bornyl acetate induces an electroantennogram (EAG) response in isolated P. americana (American cockroach) antennae from both male and female cockroaches that is similar to the response induced by sex pheromones.3 It also induces hydrogen peroxide production and apoptosis in M. polymorpha plant cells.4

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Bardyshev, I.I., and Pertsovskii, A.L. Chemical composition of oxygen-containing gum turpentine fractions from Pinus silvestris. Dokl. Akad. Nauk BSSR 13(7), 617-620 (1969).

    2. Oritani, T., and Yamashita, K. Microbial resolution of (±)-borneolst. Agr. BioI. Chem. 38(10), 1961-1964 (1974).

    3. Washio, H., and Nishino, C. Electroantennogram responses to the sex pheromone and other odours in the American cockroach. J. Insect Physiol. 22(5), 735-741 (1976).

    4. Izumi, S., Nishio, Y., Takashima, O., et al. Monoterpenoids, potent inducers of apoptosis in the cells of Marchantia polymorpha. Chem. Lett. 26(8), 837-838 (1997).