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Amylcinnamaldehyde

Base Information Edit
  • Chemical Name:Amylcinnamaldehyde
  • CAS No.:122-40-7
  • Molecular Formula:C14H18O
  • Molecular Weight:202.296
  • Hs Code.:2919.29
  • European Community (EC) Number:204-541-5,800-696-3,215-565-0
  • NSC Number:6649
  • UNII:86L63D4ZJ7
  • DSSTox Substance ID:DTXSID80859230
  • Wikipedia:Jasminaldehyde
  • Wikidata:Q27269750
  • Metabolomics Workbench ID:44812
  • ChEMBL ID:CHEMBL1989481
  • Mol file:122-40-7.mol
Amylcinnamaldehyde

Synonyms:2-pentylcinnamaldehyde;alpha-amylcinnamic aldehyde

Suppliers and Price of Amylcinnamaldehyde
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • α-AmylcinnamaldehydestabilizedwithBHT
  • 10ml
  • $ 65.00
  • TRC
  • α-AmylcinnamaldehydestabilizedwithBHT
  • 5ml
  • $ 50.00
  • TRC
  • α-AmylcinnamaldehydestabilizedwithBHT
  • 100ml
  • $ 95.00
  • TCI Chemical
  • alpha-Amylcinnamaldehyde >90.0%(GC)
  • 25mL
  • $ 20.00
  • TCI Chemical
  • alpha-Amylcinnamaldehyde >90.0%(GC)
  • 500mL
  • $ 86.00
  • Sigma-Aldrich
  • α-Amylcinnamaldehyde mixtureofcisandtrans,≥97%,natural,FG
  • 1 kg
  • $ 412.00
  • Sigma-Aldrich
  • α-Amylcinnamaldehyde mixture of
  • 1kg-k
  • $ 412.00
  • Sigma-Aldrich
  • α-Amylcinnamaldehyde mixtureofcisandtrans,≥97%,stabilized,FG
  • 10 kg
  • $ 264.00
  • Sigma-Aldrich
  • α-Amylcinnamaldehyde mixture of
  • 10kg-k
  • $ 264.00
  • Sigma-Aldrich
  • alpha-Amylcinnamaldehyde solution certified reference material, 2000?μg/mL in methanol, ampule of 1?mL
  • 1 mL
  • $ 94.50
Total 150 raw suppliers
Chemical Property of Amylcinnamaldehyde Edit
Chemical Property:
  • Appearance/Colour:clear to pale yellow liquid 
  • Vapor Pressure:0.00233mmHg at 25°C 
  • Melting Point:80°C 
  • Refractive Index:1.555 - 1.560 
  • Boiling Point:288.499 °C at 760 mmHg 
  • Flash Point:131.139 °C 
  • PSA:17.07000 
  • Density:0.963 g/cm3 
  • LogP:3.84920 
  • Storage Temp.:2-8°C 
  • Solubility.:Insoluble in water 
  • Water Solubility.:181.69mg/L at 25℃ 
  • XLogP3:4.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:6
  • Exact Mass:202.135765193
  • Heavy Atom Count:15
  • Complexity:199
Purity/Quality:

98% *data from raw suppliers

α-AmylcinnamaldehydestabilizedwithBHT *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi,N 
  • Statements: 36/37/38-51/53-43 
  • Safety Statements: 26-37/39-61-36/37 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCC(=CC1=CC=CC=C1)C=O
  • Isomeric SMILES:CCCCC/C(=C\C1=CC=CC=C1)/C=O
  • Description Amylcinnamic aldehyde is an oxidation product of amylcinnamic alcohol, one component of the "fragrance mix" and can be found as a sensitizer in cases of contact dermatitis in bakers.
  • Uses amyl cinnamal is used as a fragrance. Although it is naturally occurring in some plants, it is most often synthetically derived when used in cosmetic products. Amylcinnamaldehyde is a flavoring agent that is a yellow liquid with an odor similar to jasmine. It is insoluble in glycerin and propylene, soluble in fixed oils and mineral oil. It is obtained by chemical synthesis. It can be used alone or in combination with other flavoring substances or adjuvants. It is also termed amylcinnomaldehyde. Raw material in the production of perfumes; some perfumery uses (tuberose; peach; cherry; Estee; honeysuckle Chevrefeuille) Cross: amylcinnamic alcohol. AMYL CINNAMAL
Technology Process of Amylcinnamaldehyde

There total 10 articles about Amylcinnamaldehyde which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With benzoic acid; L-proline; In neat (no solvent); at 125 ℃; for 1h; Reagent/catalyst; Time; Inert atmosphere;
Guidance literature:
With potassium hydroxide; Aliquat 336; at 118 ℃; for 0.0166667h; Irradiation;
DOI:10.1080/00397919408011718
Guidance literature:
With sodium hydroxide; In water; at 30 ℃; for 72h;
DOI:10.1016/j.apcata.2013.06.015
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