NERYLACETONE
- Product Name
- NERYLACETONE
- CAS No.
- 3879-26-3
- Chemical Name
- NERYLACETONE
- Synonyms
- 5,9-Undecadien-2-one, 6,10-dimethyl-, (Z)-;CIS-GERANYLACETONE;NERYLACETONE;(Z)-6,10-Dimethyl-5,9-undecadien-2-one;CIS-6,10-DIMETHYLUNDECA-5,9-DIEN-2-ONE;(Z)-6,10-Dimethylundeca-5,9-dien-2-one;(7Z)-6,10-dimethylundeca-5,9-dien-2-one;(5Z)-6,10-Dimethyl-5,9-undecadien-2-one;(5Z)-6,10-dimethylundeca-5,9-dien-2-one;(5Z)-6,10-Dimethyl-5,9-undecadiene-2-one
- CBNumber
- CB7434729
- Molecular Formula
- C13H22O
- Formula Weight
- 194.31
- MOL File
- 3879-26-3.mol
NERYLACETONE Property
- Boiling point:
- 250-255 °C
- Density
- 0.868 g/mL at 20 °C(lit.)
- refractive index
- n20/D 1.467
- storage temp.
- 2-8°C
- Odor
- at 100.00 %. fatty metallic
- Odor Type
- fatty
- LogP
- 4.129 (est)
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H411Toxic to aquatic life with long lasting effects
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P321Specific treatment (see … on this label).
P332+P313IF SKIN irritation occurs: Get medical advice/attention.
P362Take off contaminated clothing and wash before reuse.
N-Bromosuccinimide Price
- Product number
- FFG0000782
- Product name
- NERYLACETONE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $505.54
- Updated
- 2021/12/16
NERYLACETONE Chemical Properties,Usage,Production
Uses
Nerylacetone is an intermediate in the synthesis of cis-Nerolidol (N390125), one of the main component in the essential oils from fresh aerial parts of Thymus ciliatus (Lamiaceae). Also, it is a terpene that displays high potency on the contractility of cardiac muscle in guinea pig left atrium. A potential and effective treatment for malaria.
Synthesis Reference(s)
Journal of the American Chemical Society, 97, p. 6870, 1975 DOI: 10.1021/ja00856a049
The Journal of Organic Chemistry, 38, p. 4082, 1973 DOI: 10.1021/jo00987a035