Photo credits: ScenTree SAS
| Company | Ingredient Name | Learn more | Naturality | Certifications | MOQ | Purity |
|---|---|---|---|---|---|---|
|
GAMMA DODECALACTONE
GDO-1
|
Discover | - | 10 grs | 98.00 - 100.00 | |
|
(R) GAMMA DODECALACTONE
M_0066060
|
Discover | Naturel | - | - | |
|
(S) GAMMA DODECALACTONE
M_0055437
|
Discover | Naturel | - | - | |
|
Gamma Dodecalactone | Discover | Synthetic Aroma Chemicals | - | - | |
|
Gamma Dodecalactone natural | Discover | Natural Aroma Chemicals | - | - |
General Presentation
-
CAS N° :
2305-05-7 -
EINECS number :
218-971-6 -
FEMA number :
2400 -
FLAVIS number :
10,019
-
JECFA number :
235 -
Volatility :
Base -
Price Range :
€€€
Physico-chemical properties
-
Appearance :
Colorless liquid -
Density :
0,935 -
Refractive Index @20°C :
1,451 - 1,456 -
Optical rotation :
Donnée indisponible. -
Vapor pressure :
Donnée indisponible. -
Flash Point :
110°C (230°F)
-
Molecular formula :
C12H22O2 -
Molecular Weight :
198,31 g/mol -
Log P :
3,55 -
Fusion Point :
Donnée indisponible. -
Boiling Point :
311°C (591,8°F) -
Detection Threshold :
Donnée indisponible.
Chemistry & Uses
Uses in perfumery :
Used to bring warm, creamy facets. Very good with fruity notes. Also used to "smooth" a accord.
Year of discovery :
Data not available.
Natural availability :
Data not available.
Isomerism :
Gamma-Dodecalactone has an asymetric carbon. Nevertheless, we always use its racemic mixture in perfumery. Delta-dodécalactone is an isomer of Decalactone-Gamma, which has one less carbon atom into its ring, but one more in its ramified carbon chain. The resulting odor changes from a metallic peach and coconut odor to a fruity peach odor
Synthesis precursor :
Gamma-Dodecalactone is not a precursor to the synthesis of another compound of olfactory interest.
Synthesis route :
Gamma-Dodecalactone is part of the gamma-lactone family: cyclic esters whose ring is made up of five atoms. This molecule is a cyclic lactone synthesized in the similar way as other lactones. The reaction between acrylic acid and butanol, in the presence of an alkaline sulphate or phosphate allows this molecule to be synthesized. Intramolecular esterification of 4-hydroxyheptanoic acid, catalyzed by a strong acid such as concentrated sulfuric acid, also makes it possible. Finally, biochemical synthesis routes are being studied by the producing companies.
Stability :
Lactones tend to polymerize through time, making them more viscous and leading to a phase shift in alcohol.
Other comments :
Data not available.
Labelling
Allergens :
This ingredient does not contain any allergen.
Signal word :
Warning
Hazard pictograms :
Precautionary statements :
| HAZARD | PRECAUTION |
|---|---|
| H315 Causes skin irritation.
H317 May cause an allergic skin reaction. H319 Causes serious eye irritation. H335 May cause respiratory irritation. H410 Very toxic to aquatic life with long lasting effects. |
P261 Avoid breathing dust/fume/gas/mist/vapours/spray. P264 Wash ... thoroughly after handling. P271 Use only outdoors or in a well-ventilated area. P280 Wear protective gloves/protective clothing/eye protection/face protection. P302 + P352 IF ON SKIN: Wash with plenty of water/… P304 + P340 IF INHALED: Remove person to fresh air and keep comfortable for breathing. P305 + P351 + P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P312 Call a POISON CENTER/doctor/… if you feel unwell. P321 Specific treatment (see ... on this label). P332 + P313 If skin irritation occurs: Get medical advice/attention. P337 + P313 If eye irritation persists: Get medical advice/attention. P362 Take off contaminated clothing. P403 + P233 Store in a well-ventilated place. Keep container tightly closed. P405 Store locked up. P501 Dispose of contents/container to… |
IFRA
IFRA 51th :
This ingredient is not restricted for the 51th amendment