Hydroxycitronellal
Product Description
Product Detail
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Product Name: |
hydroxycitronellal |
|
CAS: |
107-75-5 |
|
MF: |
C10H20O2 |
|
MW: |
172.26 |
|
EINECS: |
203-518-7 |
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Mol File: |
107-75-5.mol |
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|
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Melting point |
22-23 °C |
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Boiling point |
257 °C(lit.) |
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density |
0.923 g/mL at 25 °C(lit.) |
|
FEMA |
2583 | HYDROXYCITRONELLAL |
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refractive index |
n20/D 1.448(lit.) |
|
Fp |
>230 °F |
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storage temp. |
room temp |
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pka |
15.31±0.29(Predicted) |
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form |
Liquid |
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Specific Gravity |
0.93 |
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color |
Clear colorless |
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JECFA Number |
611 |
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InChIKey |
WPFVBOQKRVRMJB-UHFFFAOYSA-N |
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CAS DataBase Reference |
107-75-5(CAS DataBase Reference) |
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NIST Chemistry Reference |
Hydroxycitronellal(107-75-5) |
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EPA Substance Registry System |
Octanal, 7-hydroxy-3,7-dimethyl- (107-75-5) |
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Hazard Codes |
Xi |
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Risk Statements |
38-41-43 |
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Safety Statements |
26-39-36/37 |
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RIDADR |
UN1230 - class 3 - PG 2 - Methanol, solution |
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WGK Germany |
1 |
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RTECS |
RG7850000 |
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HS Code |
29124990 |
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Description |
Hydroxycitronellal has an intense, sweet, floral, lily-type odor. It may be prepared by hydration of natural citronellal obtained from Java citronella or from Eucalyptus citriodora; P-pinene is converted to myrcene, which on hydration may yield either linalool or a mixture of geranoil and nerol; the latter mixture can be hydrogenated to citronellol and subsequently converted to citronellal and hydroxycitronellal; also by hydrogenation of 3,7-dimethyl- 7-hydroxy-2-octen-2-al over palladium carbon in ethyl acetate solution. |
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Chemical Properties |
Hydroxycitronellal has a sweet, floral, lily-type odor |
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Chemical Properties |
clear colourless liquid |
|
Chemical Properties |
This is a colorless,
slightly viscous liquid with a floral odor reminiscent of linden blossom and
lily of the valley. Commercially available “hydroxycitronellal” is either
optically active or racemic, depending on the starting material used.
Hydroxydihydrocitronellal prepared from (+)-citronellal, for example, has a
specific relation α20 D +9 to +10°. |
|
Definition |
ChEBI: The tertiary alcohol arising from addition of water across the C2C double bond of citronellal. |
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Taste threshold values |
Taste characteristics at 50 ppm: sweet, waxy, green, floral and melon notes. |
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Trade name |
Laurinal® (Takasago). |
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Contact allergens |
Hydroxycitronellal is a classical fragrance allergen, found in many products. It is contained in “fragrance mix.” It has to be listed by name in the cosmetics of the EU. |
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Safety Profile |
A skin irritant. Combustible liquid. When heated to decomposition it emits acrid smoke and irritating fumes. See also ALDEHYDES. |
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Chemical Synthesis |
By hydration of natural citronellal obtained from Java citronella or from Eucalyptus citriodora; β-pinene is converted to myrcene, which on hydration may yield either linalool or mixture of geranoil and nerol; the latter mixture can be hydrogenated to citronellol and subsequently converted to citronellal and hydroxycitronellal; also by hydrogenation of 3,7-dimethyl-7-hydroxy-2- octen-2-al over palladium carbon in ethyl acetate solution. |
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Raw materials |
Sodium bisulfite-->Sodium acetate trihydrate-->SULFATE STANDARD-->Citral-->SULFUROUS ACID-->Citronellal-->Eucalyptus Citriodara Oil-->Citronella oil-->sulfurous acid |
|
Preparation Products |
8,8-Dimethoxy-2,6-dimethyloctan-2-ol-->HYDROXY CITRONELLAL DIETHYL ACETAL |