Geranylacetate , 10mMinDMSO , 105-87-3
Synonym(s):
trans-3,7-Dimethyl-2,6-octadien-1-yl acetate;trans-3,7-Dimethyl-2,6-octadienyl acetate
CAS NO.:105-87-3
Empirical Formula: C12H20O2
Molecular Weight: 196.29
MDL number: MFCD00015037
EINECS: 203-341-5
Pack Size | Price | Stock | Quantity |
1ml | RMB159.20 | In Stock |
|
others | Enquire |
PRODUCT Properties
Melting point: | 25°C |
Boiling point: | 236-242 °C(lit.) |
Density | 0.916 g/mL at 25 °C |
vapor density | 6.8 (vs air) |
vapor pressure | 0.07 mm Hg ( 20 °C) |
refractive index | n |
FEMA | 2509 | GERANYL ACETATE |
Flash point: | 220 °F |
storage temp. | 2-8°C |
solubility | Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly) |
form | Liquid |
color | Colourless |
Specific Gravity | 0.916 |
Odor | at 100.00 %. floral rose lavender green waxy |
Odor Type | floral |
Water Solubility | <0.1 g/100 mL at 20 ºC |
JECFA Number | 58 |
LogP | 4.04 at 20℃ |
Description and Uses
Geranyl acetate is a monoterpene that has been found in C. sativa with diverse biological activities. It reduces compound action potential (CAP) peak amplitude in isolated frog sciatic nerves (IC50 = 0.51 mM). Geranyl acetate inhibits the radial growth of M. gypsum, T. vercossum, and C. tropicalis on solid media. It is sporicidal against B. subtilis when used at a concentration of 1% in an agar diffusion assay. Geranyl acetate inhibits growth of COLO 205 cells (IC50 = 30 μM) via induction of DNA damage, cell cycle arrest at the G2/M phase, and mitochondrial apoptosis.
Perfumery, flavoring
Safety
Symbol(GHS) | GHS07 |
Signal word | Warning |
Hazard statements | H315-H317-H412 |
Precautionary statements | P261-P264-P272-P273-P280-P302+P352 |
Hazard Codes | Xi |
Risk Statements | 36/37/38 |
Safety Statements | 26-36-24/25 |
RIDADR | UN1230 - class 3 - PG 2 - Methanol, solution |
WGK Germany | 3 |
RTECS | RG5920000 |
F | 10-23 |
Hazard Note | Irritant |
TSCA | Yes |
HS Code | 29153900 |
Toxicity | The acute oral UD 50 value in rats was reported as 6.33 g/kg (Jenner, Hagan, Taylor, Cook & Fitzhugh, 1964). |