| Identification | Back Directory | [Name]
DIHYDRO CUMINYL ALCOHOL | [CAS]
536-59-4 | [Synonyms]
perilla
Perillol
perill alcohol
PERILLA ALCOHOL
1-perillalcohol
Perillic alcohol
PERILLYL ALCOHOL
1,8-p-Menthadien-7-ol
L-(-)-Perilly Alcohol
p-Mentha-1,8-dien-7-ol
DIHYDRO CUMINYL ALCOHOL
PARA-MENTHA-1,8-DIEN-7-OL
L(-)-Perillyl alcohol,85%
PERILLYL ALCOHOL, (-)-(RG)
(S)-(-)-PERILLYL ALCOHOL 90+%
4-isopropenylcyclohex-1-en-1-ylmethanol
4-Isopropenyl-cyclohex-1-ene-1-methanol
(4-Isopropenyl-1-cyclohexen-1-yl)methanol
(4-prop-1-en-2-yl-1-cyclohexenyl)methanol
4-(1-Methylvinyl)-1-cyclohexene-1-methanol
4-(1-methylethenyl)-1-cyclohexene-1-methano
4-(1-methylethenyl)-1-Cyclohexene-1-methanol
4-(1-methylethenyl)-cyclohex-1-ene-1-methano
4-(Prop-1-en-2-yl)-cyclohex-1-enyl)-methanol
1-HYDROXYMETHYL-4-(1-METHYLVINYL)-CYCLOHEXENE
(4-(prop-1-en-2-yl)cyclohex-1-en-1-yl)Methanol
Perilla alcohol
Dihydrocuminyl alcohol
1-Cyclohexene-1-methanol, 4-(1-methylethenyl)-
Cyclohex-1-ene-1-methanol, 4-(1-methylethenyl)- | [EINECS(EC#)]
208-639-9 | [Molecular Formula]
C10H16O | [MDL Number]
MFCD00001567 | [MOL File]
536-59-4.mol | [Molecular Weight]
152.23 |
| Chemical Properties | Back Directory | [Appearance]
clear colorless to light yellow liquid | [Melting point ]
271-272 °C | [Boiling point ]
119-121 °C11 mm Hg(lit.)
| [density ]
0.96 g/mL at 25 °C(lit.)
| [FEMA ]
2664 | [refractive index ]
n20/D 1.501(lit.)
| [Fp ]
>230 °F
| [storage temp. ]
Inert atmosphere,2-8°C | [pka]
14.85±0.10(Predicted) | [Odor]
at 100.00 %. green cumin spicy aromatic woody cardamom floral waxy violet | [Odor Type]
green | [JECFA Number]
974 | [LogP]
3.170 | [CAS DataBase Reference]
536-59-4 | [EPA Substance Registry System]
1-Cyclohexene-1-methanol, 4-(1-methylethenyl)- (536-59-4) |
| Hazard Information | Back Directory | [Chemical Properties]
clear colorless to light yellow liquid | [Usage]
antineoplastic, apoptosis inducer; skin irritant, LD50(rat) 2100 mg/kg po | [Description]
p-Mentha-1,8-dien-7-ol has a characteristic odor similar to linalool
and terpineol. The L-form is obtained starting from (3-pinene or by
reducing perillic aldehyde with zinc dust and acetic acid, followed
by saponification of the acetate. | [Occurrence]
The d- and l-forms occur naturally in gingergrass essential oil; the l-form is found in lavandin and bergamot,
while the d-form is found in caraway; also reported found in the essential oils of Juniperus sabina L. and East Indian geranium. Also
reported found in citrus peel oils, berries, peppermint oil, Scotch peppermint oil, hop oil, cardamom, laurel, lemon balm, lamb’s let tuce, mastic gum oil and bullock’s head (Annona reticulata). | [Uses]
(4-(Prop-1-en-2-yl)cyclohex-1-en-1-yl)methanol is used in preparation of perilla alcohol leaf alcohol carbonate as perfume. | [Uses]
antineoplastic, apoptosis inducer; skin irritant, LD50(rat) 2100 mg/kg po | [Definition]
ChEBI: A limonene monoterpenoid consists of a cyclohexene ring substituted by a hydroxymethyl and a prop-1-en-2-yl group at positions 1 and 4 respectively. It is a constituent of a variety of essential oils including lavender. | [Preparation]
The l-form is obtained starting from β-pinene or by reducing perillic aldehyde with zinc dust and acetic acid, followed
by saponification of the acetate. | [Aroma threshold values]
Detection: 7 ppm |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
37/38-41 | [Safety Statements ]
26-39 | [WGK Germany ]
3
| [RTECS ]
OS8395000
| [HS Code ]
29061990 | [Safety Profile]
Moderately toxic by ingestion. A severe skin irritant. Combustible liquid. When heated to decomposition it emits acrid smoke and irritating fumes. | [Toxicity]
LD50 orl-rat: 2100 mg/kg FCTXAV 19,253,81 |
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