| Identification | More | [Name]
DL-Isoborneol | [CAS]
124-76-5 | [Synonyms]
BORNEOL(ISO)
DL-ISOBORNEOL
DL-ISOBORNYL ALCOHOL
DL-ISOCAMPHAL
EXO-1,7,7-TRIMETHYLBICYCLO(2.2.1)-2-HEPTANOL
EXO-2-CAMPHANOL
FEMA 2158
(+/-)-ISOBORNEOL
ISOBORNEOL
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol
1,7,7-Trimethyl-bicyclo[2.2.1]heptan-2-ol (isoborneol)
1,7,7-trimethyl-exo-Bicyclo[2.2.1]heptan-2-ol
2-exo-Borneol
2-exo-Bornylalcohol
7,7-trimethyl-exo-bicyclo(2.2.1)heptan-2-o
7,7-trimethyl-exo-bicyclo[2.2.1]heptan-2-o
Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, exo-
Bicyclo[2.2.1]heptan-2-ol,1,7,7-trimethyl-,(1R,2R,4R)-rel-
Bicyclo[2.2.1]heptan-2-ol,1,7,7-trimethyl-,1R,2R,4R-rel-
Bicyclo[2.2.1]heptan-2-ol,1,7,7-trimethyl-,exo- | [EINECS(EC#)]
204-712-4 | [Molecular Formula]
C10H18O | [MDL Number]
MFCD00074821 | [Molecular Weight]
154.25 | [MOL File]
124-76-5.mol |
| Chemical Properties | Back Directory | [Definition]
A geometrical isomer of borneol. | [Appearance]
white to almost white crystalline powder | [Melting point ]
212-214 °C (subl.)(lit.)
| [Boiling point ]
214°C | [density ]
0.8389 (rough estimate) | [vapor pressure ]
0.057-4.706Pa at 25℃ | [FEMA ]
2158 | [refractive index ]
1.4710 (estimate) | [Fp ]
200 °F
| [storage temp. ]
2-8°C | [solubility ]
almost transparency in Methanol | [form ]
Powder | [pka]
15.36±0.60(Predicted) | [color ]
Yellow | [Odor]
at 10.00 % in dipropylene glycol. balsam camphor herbal woody | [Odor Type]
balsamic | [Water Solubility ]
insoluble | [JECFA Number]
1386 | [Merck ]
14,5128 | [BRN ]
4126091 | [LogP]
2.32-2.92 at 20-25℃ | [CAS DataBase Reference]
124-76-5(CAS DataBase Reference) | [NIST Chemistry Reference]
DL-Isoborneol(124-76-5) | [EPA Substance Registry System]
124-76-5(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
F,Xi | [Risk Statements ]
R11:Highly Flammable.
R38:Irritating to the skin. | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [RIDADR ]
UN 1312 4.1/PG 3
| [WGK Germany ]
2
| [RTECS ]
NP7300000
| [TSCA ]
Yes | [HazardClass ]
4.1 | [HS Code ]
29061900 | [Hazardous Substances Data]
124-76-5(Hazardous Substances Data) | [Toxicity]
mouse,LD50,intravenous,56mg/kg (56mg/kg),U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#03209, |
| Hazard Information | Back Directory | [Description]
Isoborneol has a piney, camphoraceous odor. May be prepared by
the hydrolysis of isobomyl acetate, or by catalytic reduction of
camphor (both d- and ι-isomers); the optically inactive compound
can be prepared by treating camphene with a 1:1 mixture of sulfuric acid and glacial acetic acid and then hydrolyzing the
isobomyl acetat. | [Chemical Properties]
Isoborneol has a piney, camphoraceous odor. | [Chemical Properties]
white to almost white crystalline powder | [Occurrence]
Reported found in the oil of Abies sibirica and a few other essences and in the essential oil from roots of
Chamaeciparis formosensis. Also reported found in apple, papaya, blackberry, cinnamomum, ginger, thymus, cheeses, cognac,
Ocimum basilicum, rosemary, temoe lawak (Curcuma xanthorriza Roxb.) turmeric, sage, clary sage, ashanti pepper, German chamomile oil, eucalyptus oil and mastic gum leaf oil | [Uses]
Isoborneol is a monoterpene and a component of several plant essential oils, showed dual viricidal activity against herpes simplex virus 1 (HSV-1). | [Preparation]
By the hydrolysis of isobornyl acetate, or by catalytic reduction of camphor (both d- and l-isomers); the optically inactive
compound can by prepared by treating camphene with a 1:1 mixture of sulfuric acid and glacial acetic acid and then hydrolyzing the
isobornyl acetate | [Aroma threshold values]
Detection: 2.5 to 16 ppb | [General Description]
Isoborneol is a monoterpene and a known antioxidant, which is a component of several plant essential oils. | [Flammability and Explosibility]
Flammable | [Purification Methods]
Crystallise isoborneol from EtOH or pet ether (b 60-80o). It sublimes in a vacuum. The 4-nitrobenzoyl derivative has m 153o. [Yager & Morgan J Am Chem Soc 57 2081 1935, Beilstein 6 II 80, 6 III 299, 6 IV 281.] |
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