Eucalyptus oil

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Catalog Number : CS-BQ-00017
CAS Number : 8000-48-4
Status :
Category : Pesticide Standards
Industry : Flavours and Fragrances
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Canonical SMILES : CC1(C2CCC(O1)(CC2)C)C
Isomeric SMILES : CC1(C2CCC(O1)(CC2)C)C
InChI : InChI=1S/C10H18O/c1-9(2)8-4-6-10(3,11-9)7-5-8/h8H,4-7H2,1-3H3
InchIKey : WEEGYLXZBRQIMU-UHFFFAOYSA-N
IUPAC Name : 1,3,3-trimethyl-2-oxabicyclo[2.2.2]octane
Exact Mass : 154.135765193
Color : Colorless liquid or oil
Odor : Camphor-like odor
Melting Point : 34.7 °F (NTP, 1992)
Boiling Point : 349 to 351 °F at 760 mm Hg (NTP, 1992)
Solubility : Insoluble (<1 mg/ml at 68° F) (NTP, 1992)
Density : 0.921 to 0.923 (NTP, 1992)
Chemical Classes : Biological Agents -> Plant Oils and Extracts
Use Classification : EPA Safer Chemical Functional Use Classes -> Fragrances
Industry Uses : Odor agents
Consumer Uses : Air care products
Hazard Class : Flam. Liq. 3 (83.6%)
Description : 1,8-cineole is a cineole. It has a role as a flavouring agent.
Disposal Methods : SRP: Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in air, soil or water; effects on animal, aquatic and plant life; and conformance with environmental and public health regulations. If it is possible or reasonable use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination.
EC Number : 207-431-5
Vapor Pressure : 1.90 mmHg
Toxicity Summary : Oral, rat LD50: 2480 mg/kg
Antidoteand Emergency Treatment : Immediate first aid: Ensure that adequate decontamination has been carried out. If patient is not breathing, start artificial respiration, preferably with a demand-valve resuscitator, bag-valve-mask device, or pocket mask, as trained. Perform CPR as necessary. Immediately flush contaminated eyes with gently flowing water. Do not induce vomiting. If vomiting occurs, lean patient forward or place on left side (head-down position, if possible) to maintain an open airway and prevent aspiration. Keep patient quiet and maintain normal body temperature. Obtain medical attention. /Camphor and Related Compounds/
Human Toxicity Excerpts : /ALTERNATIVE and IN VITRO TESTS/ The purpose of this test was to evaluate the skin irritation potential of eucalyptol using the EPISKIN (TM) reconstructed human epidermis model after a treatment period of 15 minutes followed by a post-exposure incubation period of 42 hours. The principle of the assay was based on the measurement of cytotoxicity in reconstructed human epidermal cultures following topical exposure to eucalyptol by means of the colorimetric MTT reduction assay. Cell viability is measured by enzymatic reduction of the yellow MTT tetrazolium salt (3 -[4,5-dimethylthiazol-2-yl]-2,5-diphenyl-tetrazolium bromide) to a blue formazan salt (within the mitochondria of viable cells) in the eucalyptol treated tissues relative to the negative controls. The concentration of the inflammatory mediator IL-1a in the culture medium retained following the 42-hour post-exposure incubation period is also determined for eucalyptol which are found to be borderline non-irritant based upon the MTT reduction endpoint. This complimentary end-point will be used to either confirm a non-irritant result or will be used to override the non-irritant result. This method was designed to be compatible with the following: OECD Guidelines for the Testing of Chemicals No. 439 In VitroSkin Irritation (adopted 22 July 2010) Method B.46 of Commission Regulation (EC) No. 440/2008/EC Triplicate tissues were treated with eucalyptol for an exposure period of 15 minutes. At the end of the exposure period each tissue was rinsed before incubating for 42 hours. At the end of the post-exposure incubation period each tissue was taken for MTT-loading. The maintenance medium from beneath each tissue was transferred to pre-labelled micro tubes and stored in a freezer for possible inflammatory mediator determination. After MTT loading a total biopsy of each epidermis was made and placed into micro tubes containing acidified isopropanol for extraction of formazan crystals out of the MTT-loaded tissues. At the end of the formazan extraction period each tube was mixed thoroughly and duplicate 200 ul samples were transferred to the appropriate wells of a pre-labelled 96 -well plate. The optical density was measured at 540 nm. Data are presented in the form of percentage viability (MTT reduction in the test item treated tissues relative to negative control tissues). The relative mean viability of the test item treated tissues was 88.9% after the 15-Minute exposure period. The quality criteria required for acceptance of results in the test were satisfied. Eucalyptol was considered to be Non-Irritant (NI).

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