cyclamen homoaldehyde
silvial (Givaudan)
 
Notes:
None found
  • BOC Sciences
    • BOC Sciences
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      Product(s):
      6658-48-6 Benzenepropanal, a-methyl-4-(2-methylpropyl)-
       
  • Lluch Essence
    • Lluch Essence S.L.
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  • Moellhausen
  • Pell Wall Perfumes
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      Silvial
      Arctander thought the material had potential for wider use: “The title aldehyde, commercially available for some years, has some of the advantages of Cyclamen aldehyde, and some of those of Lilial (Bucinal), its tertiary-Butyl-isomer. It is undoubtedly more versatile than Cyclamen aldehyde, and the perfumer can enjoy using much higher concentrations of this aldehyde, without producing overly green-vegetable notes, etc”
       
       
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      Product(s):
      09-43500 P-ISOBUTYL-ALPHA-METHYLHYDROCINNAMALDEHYDE
       
  • Vigon International
    • Vigon International
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      Manufacturer and supplier of high quality flavor and fragrance ingredients.
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      Product(s):
      502042 Silvial
       
Synonyms   Articles   Notes   Search
Fragrance Demo Formulas
CAS Number: 6658-48-6Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 229-695-0
FDA UNII: Search
Nikkaji Web: J298.050I
XlogP3-AA: 3.80 (est)
Molecular Weight: 204.31260000
Formula: C14 H20 O
NMR Predictor: Predict (works with chrome, Edge or firefox)
Category: fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
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Physical Properties:
Appearance: colorless clear liquid (est)
Assay: 96.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 285.00 to  286.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.003000 mmHg @ 25.00 °C. (est)
Flash Point: 273.00 °F. TCC ( 133.89 °C. )
logP (o/w): 4.034 (est)
Soluble in:
 alcohol
 water, 7.299 mg/L @ 25 °C (est)
Stability:
 alcoholic fine fragrances - good
 antiperspirants - good
 concentrated fabric softeners - good
 hypochlorite bleach - poor
 liquid detergent - good
 perborate powder detergent - good
 soaps - good
 toiletry applications - good
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: floral
 
Odor Strength: medium
 
Substantivity: 336 hour(s) at 100.00 %
 
 floral  muguet  lily  green  tropical  oily  greasy  marine  balsamic  
Odor Description:
at 100.00 %. 
floral muguet lily green tropical oily greasy marine balsamic
Luebke, William tgsc, (2016)
 
Odor and/or flavor descriptions from others (if found).
 
Givaudan
Silvial®
Odor Description: Powerful, Floral, Muguet, Fresh
Silvial is a powerful, vibrant muguet ingredient with a slight citrus undertone and a fresh, aldehydic touch that is used in perfumery in the same way as related muguet products.
 
Takasago
Suzaral ® ≥96%
Odor Description: Floral, Green, Aldehydic, Marine
A popular component of flower compositions, particularly lily of the valley and linden types providing a pleasant blossom odor.
 
Pell Wall Perfumes
Silvial
Odor Description: Floral-muguet, fresh-marine, aldehydic, green, balsamic
Arctander thought the material had potential for wider use: “The title aldehyde, commercially available for some years, has some of the advantages of Cyclamen aldehyde, and some of those of Lilial (Bucinal), its tertiary-Butyl-isomer. It is undoubtedly more versatile than Cyclamen aldehyde, and the perfumer can enjoy using much higher concentrations of this aldehyde, without producing overly green-vegetable notes, etc”
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
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Suppliers:
BOC Sciences
For experimental / research use only.
Benzenepropanal, a-methyl-4-(2-methylpropyl)-
Creatingperfume.com
Silvial® (Givaudan)
Odor: Powerful, Floral, Muguet, Fresh
Givaudan
Silvial®
Odor: Powerful, Floral, Muguet, Fresh
Use: Silvial is a powerful, vibrant muguet ingredient with a slight citrus undertone and a fresh, aldehydic touch that is used in perfumery in the same way as related muguet products.
Lluch Essence
SILVIAL
Moellhausen
SILVIAL
Pell Wall Perfumes
Silvial
Odor: Floral-muguet, fresh-marine, aldehydic, green, balsamic
Use: Arctander thought the material had potential for wider use: “The title aldehyde, commercially available for some years, has some of the advantages of Cyclamen aldehyde, and some of those of Lilial (Bucinal), its tertiary-Butyl-isomer. It is undoubtedly more versatile than Cyclamen aldehyde, and the perfumer can enjoy using much higher concentrations of this aldehyde, without producing overly green-vegetable notes, etc”
Penta International
P-ISOBUTYL-ALPHA-METHYLHYDROCINNAMALDEHYDE
Perfumery Laboratory
SILVIAL Givaudan
Odor: Flower (lily), fresh sea, aldehyde, with a tinge of green
The Perfumers Apprentice
Silvial (G)
Odor: vibrant muguet ingredient with a slightly citrus aspect and a fresh, aldehydic touch
Vigon International
Silvial
Odor: Powerful, Floral, Muguet, Fresh
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Safety Information:
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
Skin corrosion/irritation (Category 3), H316
Skin sensitisation (Category 1), H317
Reproductive toxicity (Category 2), H361
Acute aquatic toxicity (Category 2), H401
Chronic aquatic toxicity (Category 2), H411
GHS Label elements, including precautionary statements
 
Pictogramhealth-hazard.jpgexclamation-mark.jpgenvironment.jpg
 
Signal word Warning
Hazard statement(s)
H316 - Causes mild skin irritation
H317 - May cause an allergic skin reaction
H361 - Suspected of damaging fertility or the unborn child
H401 - Toxic to aquatic life
H411 - Toxic to aquatic life with long lasting effects
Precautionary statement(s)
P201 - Obtain special instructions before use.
P202 - Do not handle until all safety precautions have been read and understood.
P261 - Avoid breathing dust/fume/gas/mist/vapours/spray.
P264 - Wash skin thouroughly after handling.
P272 - Contaminated work clothing should not be allowed out of the workplace.
P273 - Avoid release to the environment.
P280 - Wear protective gloves/protective clothing/eye protection/face protection.
P302 + P352 - IF ON SKIN: wash with plenty of soap and water.
P308 + P313 - IF exposed or concerned: Get medical advice/attention.
P333 + P313 - IF SKIN irritation or rash occurs: Get medical advice/attention.
P362 - Take off contaminated clothing and wash before reuse.
P391 - Collect spillage. Hazardous to the aquatic environment
P405 - Store locked up.
P501 - Dispose of contents/ container to an approved waste disposal plant.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
IFRA Critical Effect: Dermal sensitization and systemic toxicity
IFRA: View Standard
View IFRA Standards Library for complete information.
Please review Amendment 49 IFRA documentation for complete information.
IFRA RESTRICTION LIMITS IN THE FINISHED PRODUCT (%):
Category 1: Products applied to the lips
0.08 %
Category 2: Products applied to the axillae
0.053 %
Category 3: Products applied to the face/body using fingertips
0.80 %
Category 4: Products related to fine fragrance
0.99 %
 Category 5: Products applied to the face and body using the hands (palms), primarily leave-on
Category 5A: Body lotion products applied to the body using the hands (palms), primarily leave-on
0.25 %
Category 5B: Face moisturizer products applied to the face using the hands (palms), primarily leave-on
0.25 %
Category 5C: Hand cream products applied to the hands using the hands (palms), primarily leave-on
0.25 %
Category 5D: Baby Creams, baby Oils and baby talc
0.083 %
Category 6: Products with oral and lip exposure
0.080 %
 Category 7: Products applied to the hair with some hand contact
Category 7A: Rinse-off products applied to the hair with some hand contact
0.72 %
Category 7B: Leave-on products applied to the hair with some hand contact
0.72 %
Category 8: Products with significant anogenital exposure
0.083 %
Category 9: Products with body and hand exposure, primarily rinse off
1.90 %
 Category 10: Household care products with mostly hand contact
Category 10A: Household care excluding aerosol products (excluding aerosol/spray products)
1.90 %
Category 10B: Household aerosol/spray products
5.40 %
 Category 11: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate
Category 11A: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate without UV exposure
0.083 %
Category 11B: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate with potential UV exposure
0.083 %
Category 12: Products not intended for direct skin contact, minimal or insignificant transfer to skin
No Restriction
 Notes:
IFRA FLAVOR REQUIREMENTS:

Due to the possible ingestion of small amounts of fragrance ingredients from their use in products in Categories 1 and 6, materials must not only comply with IFRA Standards but must also be recognized as safe as a flavoring ingredient as defined by the IOFI Code of Practice (www.iofi.org). For more details see chapter 1 of the Guidance for the use of IFRA Standards.

 
Recommendation for cyclamen homoaldehyde flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 6658-48-6
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 110914
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 2
 2-methyl-3-[4-(2-methylpropyl)phenyl]propanal
Chemidplus: 0006658486
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References:
Leffingwell: Chirality or Article
 2-methyl-3-[4-(2-methylpropyl)phenyl]propanal
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 6658-48-6
Pubchem (cid): 110914
Pubchem (sid): 135067153
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
HMDB (The Human Metabolome Database): Search
ChemSpider: View
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Potential Blenders and core components note
 
For Odor
No odor group found for these
2-ethyl-N-methyl-N-(3-methyl phenyl) butyramideFR
aldehydic
 citronellyl oxyacetaldehydeFL/FR
 lily pentanalFR
 muguet undecadienalFR
animal
para-cresyl isobutyrateFL/FR
chemical
 propyl propionateFL/FR
citrus
 benzyl anthranilateFR
 citrus ocimenolFR
(Z)-4-decenalFL/FR
 marine decadienalFR
 myrmac aldehydeFR
 orange nitrileFR
 tetrahydromyrcenolFR
clean
sea cotton fragranceFR
earthy
 octyl phenyl acetateFL/FR
fatty
 allyl octanoateFL/FR
floral
alpha-amyl cinnamaldehyde dimethyl acetalFL/FR
 bois de rose oil brazilFL/FR
4-isobutyl cyclohexane propanalFR
 cassis specialtyFR
 citronellyl butyrateFL/FR
 citronellyl ethoxalateFR
 coranol (Firmenich)FR
 corps popinalFR
 cumin carbinolFR
 cuminyl acetaldehydeFL/FR
 cyclamen aldehyde / methyl anthranilate schiff's baseFR
 cyclohexyl propanolFR
2-decalinolFR
 dihydrolinaloolFL/FR
2,5-dimethyl-2-indan methanolFR
3,6-dimethyl-3-octanolFL/FR
4-ethyl cyclohexane propanalFR
 ethyl linaloolFR
 ethyl linalyl acetalFR
 ethyl linalyl acetateFR
 ethyl linalyl etherFL/FR
(E,E)-farnesolFL/FR
 floral butanalFR
 floral pyranolFR
 floral specialtyFR
 freesia acetateFR
 greenhouse fragranceFR
 hawthorn ethanolFR
(Z)-4-hepten-2-yl salicylateFR
 hydrangea fragranceFR
 hydroxycitronellalFL/FR
 hydroxycitronellal / methyl anthranilate schiff's baseFR
 hydroxycitronellal diethyl acetalFL/FR
 hydroxycitronellal dimethyl acetalFL/FR
 hydroxycitronellal distillation residue distillatesFR
 hydroxycitronellal nitrileFR
 hydroxycitronellal propylene glycol acetalFL/FR
 hydroxycitronellal residueFR
 hydroxycitronellolFL/FR
 jasimiaFR
 leerallFR
 leerall / methyl anthranilate schiff's baseFR
calla lily fragranceFR
 lily of the valley specialtyFR
 lily propanolFR
 lilyallFR
 lilyall / methyl anthranilate schiff's baseFR
 lilyall substituteFR
laevo-linaloolFL/FR
dextro-linaloolFL/FR
 linaloolFL/FR
 linalool oxideFL/FR
 linalyl anthranilateFL/FR
 linalyl benzoateFL/FR
 magnolia cyclohexanolFR
 magnolia decadienalFR
 methoxycitronellalFR
4-methyl cyclohexane propanalFR
2-methyl octanalFL/FR
1-methyl-3-(2-methyl propyl) cyclohexanolFR
3-methyl-6-ethyl-5-octen-1-olFR
 muguet butanalFR
 muguet butanolFR
 muguet carbaldehydeFR
 muguet carboxaldehydeFR
 muguet ethanolFR
 muguet nitrileFR
 muguet octadienolFR
 muguet propanolFR
 muguet shiseolFL/FR
 muguet specialtyFR
 octahydro-4,7-methano-1H-indene-5-acetaldehydeFR
 octahydro-4,7-methano-1H-indene-5-acetaldehyde + 6-methyl-octahydro-4,7-methano-indene-5-carbaldehydFR
 petitgrain oil fractionsFR
 phenethyl butyrateFL/FR
 phenyl glycol diacetateFR
4-propyl cyclohexane propanalFR
alpha-terpinyl anthranilateFL/FR
 tetrahydrolinaloolFL/FR
fresh
 decyl methyl etherFR
fruity
 apple ketalFL/FR
 butyl isobutyrateFL/FR
 citronellyl isobutyrateFL/FR
 cyclohexyl carboxylic acidFL/FR
 grape butyrateFL/FR
 propyl hexanoateFL/FR
green
(Z)-3-hepten-1-yl acetateFL/FR
 phenyl acetaldehyde diethyl acetalFL/FR
 phenyl hexyl acetateFR
herbal
 dimethyl benzyl carbinyl formateFL/FR
marine
green algae absoluteFL/FR
 ozone propanalFR
melon
(Z)-6-nonen-1-yl acetateFL/FR
 watermelon ketoneFR
sulfurous
 mango thiolFL/FR
(S)-1-methoxy-3-heptane thiolFL/FR
tropical
 ethyl (Z)-3-hexenoateFL/FR
2-tropical oxathianeFL/FR
woody
 hydroxycitronellal diisotridecyl acetalFR
 
For Flavor
 
No flavor group found for these
green algae absoluteFL/FR
alpha-amyl cinnamaldehyde dimethyl acetalFL/FR
 dimethyl benzyl carbinyl formateFL/FR
 ethyl (Z)-3-hexenoateFL/FR
 ethyl linalyl etherFL/FR
(E,E)-farnesolFL/FR
(Z)-3-hepten-1-yl acetateFL/FR
 hydroxycitronellal propylene glycol acetalFL/FR
dextro-linaloolFL/FR
2-methyl octanalFL/FR
 octyl phenyl acetateFL/FR
 phenyl acetaldehyde diethyl acetalFL/FR
alpha-terpinyl anthranilateFL/FR
aromatic
para-cresyl isobutyrateFL/FR
citrus
 citronellyl oxyacetaldehydeFL/FR
(Z)-4-decenalFL/FR
 linaloolFL/FR
laevo-linaloolFL/FR
fatty
 allyl octanoateFL/FR
floral
 bois de rose oil brazilFL/FR
 dihydrolinaloolFL/FR
 linalyl anthranilateFL/FR
 muguet shiseolFL/FR
 tetrahydrolinaloolFL/FR
fruity
 apple ketalFL/FR
 butyl isobutyrateFL/FR
 citronellyl butyrateFL/FR
 citronellyl isobutyrateFL/FR
 cyclohexyl carboxylic acidFL/FR
 linalyl benzoateFL/FR
(S)-1-methoxy-3-heptane thiolFL/FR
 phenethyl butyrateFL/FR
 propyl hexanoateFL/FR
green
 cuminyl acetaldehydeFL/FR
 grape butyrateFL/FR
 linalool oxideFL/FR
(Z)-6-nonen-1-yl acetateFL/FR
herbal
3,6-dimethyl-3-octanolFL/FR
melon
 hydroxycitronellal diethyl acetalFL/FR
powdery
 hydroxycitronellolFL/FR
sulfurous
 mango thiolFL/FR
tropical
 propyl propionateFL/FR
2-tropical oxathianeFL/FR
waxy
 hydroxycitronellalFL/FR
 hydroxycitronellal dimethyl acetalFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 aldehydicFR
 azaleaFR
 cyclamenFR
 fetesFR
 floralFR
 fresh and cleanFR
 lilyFR
 lily calla lilyFR
 lily ginger lilyFR
 lily of the valleyFR
 lily tiger lilyFR
 lily water lilyFR
 lotusFR
 mango flowerFR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 not found in nature
Synonyms   Articles   Notes   Search   Top
Synonyms:
 benzenepropanal, a-methyl-4-(2-methylpropyl)-
para-isobutyl-alpha-methyl hydrocinnamaldehyde
3-(4-isobutylphenyl)-2-methylpropanal
3-(p-cumenyl)-2-methyl propionaldehyde
3-(para-cumenyl)-2-methyl propionaldehyde
 cyclamen homoaldehyde
2-methyl-3-(4-(2-methyl propyl)phenyl) propanal
2-methyl-3-[4-(2-methylpropyl)phenyl]propanal
alpha-methyl-4-(2-methyl propyl) benzene propanal
a-methyl-4-(2-methylpropyl)benzenepropanal
alpha-methyl-4-(2-methylpropyl)benzenepropanal
a-methyl-4-(2-methylpropyl)benzenepropionaldehyde
 rhodial
 silvial (Givaudan)
 suzaral (Takasago)
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