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Helional Floramelon 1205-17-0
CAS: 1205-17-0
Molecular Formula: C11H12O3
Name | Floramelon |
Synonyms | Heliogan Helional Floramelon Helional[IFF] Aquanal[Quest] Heliobouquet[Takasago] 2-Methyl-3-(3,4-Methylenedioxyphenyl)Propanal alpha-methyl-1,3-benzodioxole-5-propionaldehyde α-Methyl-3,4-methylene-dioxyhydrocinnamic aldehyde |
CAS | 1205-17-0 |
EINECS | 214-881-6 |
InChI | InChI=1/C11H12O3/c1-8(6-12)4-9-2-3-10-11(5-9)14-7-13-10/h2-3,5-6,8H,4,7H2,1H3/t8-/m1/s1 |
InChIKey | BOPPSUHPZARXTH-UHFFFAOYSA-N |
Molecular Formula | C11H12O3 |
Molar Mass | 192.21 |
Density | 1.162g/mLat 25°C(lit.) |
Boling Point | 282°C(lit.) |
Flash Point | >230°F |
JECFA Number | 2212 |
Water Solubility | 934mg/L at 20℃ |
Vapor Presure | 0.092Pa at 23℃ |
Appearance | clear liquid |
Color | Light orange to Yellow to Green |
Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
Refractive Index | n20/D 1.5335(lit.) |
Use | Used in cosmetics and detergents |
FEMA | 4599 | 3-(3,4-METHYLENEDIOXYPHENYL)-2-METHYLPROPANAL |
LogP | 2.4 at 25℃ |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
Introduction | New jasmine aldehyde (English: Helional) is an aromatic organic compound, which can be regarded as a homolog of piperonal, with the structure of phenylaldehydes, Insoluble in water, soluble in alcohol, with a floral aroma, often used in commercial perfumes and odorants. |
essence and spice | piperyl propionaldehyde is a kind of fresh watermelon fragrance and light lily of the valley and jasmine-like fennel fragrance. it is widely used to prepare a variety of floral, forest and sea breeze flavors such as jasmine and rabbit ear flowers, with lasting fragrance. |
application | new jasmine aldehyde is a kind of spice widely used in the world. it has gentle floral fragrance like rabbit ear grass. in the formula of cosmetics and soap essence, the dosage is within 20%, the usage is large and the price is high. |
preparation | 100g of jasmine aldehyde, 100g of methanol, 40g of propionaldehyde, 3g of potassium hydroxide, reaction temperature 40 ℃, reaction time 1.5h, yield 71.4%. In the second step, the hydrogenation of piperonyl propionaldehyde was used to synthesize new jasmine aldehyde. The optimal reaction conditions were determined by single factor method as follows: 100g of piperonyl propionaldehyde, 100g of methanol, 5g of 5% palladium-carbon catalyst, 300KPa of absolute pressure in hydrogenation kettle, 40 ℃ of reaction temperature, 3h of reaction time and 93.1% yield. The two-step total yield is 66.5%. The structural products of the two-step reaction were characterized. Then try to synthesize new jasmine aldehyde by one-pot method, that is, the two-step reaction of synthesis and hydrogenation is completed in a hydrogenation kettle. The optimum reaction conditions were explored by orthogonal method as follows: 100g of jasmonaldehyde, 100g of methanol, 40g of propionaldehyde, 5g of 5% palladium-carbon catalyst, 3g of potassium hydroxide, 300KPa of absolute pressure in hydrogenation kettle, 40 ℃ of reaction temperature, 3h of reaction time and 64.8% yield. |
use | used in cosmetics and detergents |
Mol Download Chemical properties
CAS:
1205-17-0
MF:
C11H12O3
MW:
192.21
EINECS:
214-881-6
MDL No.:
MFCD00067053
Boiling point:
282 °C(lit.)
Density
1.162 g/mL at 25 °C(lit.)
vapor pressure
0.092Pa at 23℃
refractive index
n20/D 1.5335(lit.)
FEMA
4599 | 3-(3,4-METHYLENEDIOXYPHENYL)-2-METHYLPROPANAL
Flash point:
>230 °F
storage temp.
under inert gas (nitrogen or Argon) at 2-8°C
solubility
soluble in Chloroform, Ethyl Acetate
form
clear liquid
color
Light orange to Yellow to Green
Odor
at 100.00 %. watery fresh green ozone cyclamen hay
Odor Type
floral
Water Solubility
934mg/L at 20℃
JECFA Number
2212
InChIKey
BOPPSUHPZARXTH-UHFFFAOYSA-N
LogP
2.4 at 25℃
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