Lily aldehyde manufacturers and suppliers

Lily aldehyde suppliers

Properties

Melting point:: 106-109 °C

Boiling point:: 150°C 10mm

Density: 0.946 g/mL at 20 °C(lit.)

vapor pressure: 0.25Pa at 20℃

refractive index: n20/D 1.505

Flash point:: 100°C

storage temp.: 2-8°C

solubility: Chloroform (Sparingly), Ethyl Acetate (Slightly)

form: Liquid

color: Colorless to Light yellow

Odor: at 100.00 %. floral muguet watery green powdery cumin

Odor Type: floral

Water Solubility: 33mg/L at 20℃

BRN: 880140

Henry's Law Constant: 5.7×10^-1 mol/(m³Pa) at 25℃, Dupeux et al. (2022)

Major Application: cleaning products
cosmetics
food and beverages
personal care

Cosmetics Ingredients Functions: FRAGRANCE
PERFUMING

InChI: 1S/C14H20O/c1-11(10-15)9-12-5-7-13(8-6-12)14(2,3)4/h5-8,10-11H,9H2,1-4H3

InChIKey: SDQFDHOLCGWZPU-UHFFFAOYSA-N

SMILES: [H]C(=O)C(C)Cc1ccc(cc1)C(C)(C)C

LogP: 4.2 at 24℃

CAS DataBase Reference: 80-54-6(CAS DataBase Reference)

NIST Chemistry Reference: Lilial(80-54-6)

EPA Substance Registry System: Benzenepropanal, 4-(1,1-dimethylethyl)-.alpha.-methyl- (80-54-6)

Safety Information

Symbol(GHS): GHS07,GHS08

Signal word: Warning

Hazard statements: H302-H315-H317-H361-H412

Precautionary statements: P202-P273-P280-P301+P312-P302+P352-P308+P313

Hazard Codes: Xn,N

Risk Statements: 22-38-51/53-62-43

Safety Statements: 60-61-36/37

RIDADR: UN 3082 9/PG 3

WGK Germany: 2

RTECS: MW4895000

F: 10

TSCA: TSCA listed

HS Code: 29121900

Storage Class: 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects

Hazard Classifications: Acute Tox. 4 Oral
Aquatic Chronic 3
Repr. 1B
Skin Irrit. 2
Skin Sens. 1

REACH Registrations: Active

Use

Lily aldehyde is a homolog of cyclamenaldehyde. The racemic compound is a colorless to slightly yellow liquid with a mild-floral odor, reminiscent of cyclamen and lily of the valley. The aldehyde is prepared by the same routes as cyclamenaldehyde. Other routes start from ??-methylcinnamaldehyde. ??-Methylcinnamaldehyde (from benzaldehyde and propionaldehyde) is hydrogenated to ??-methyldihydrocinnamic alcohol.The alcohol is alkylated with tert-butyl chloride or isobutene to 4-tert-butyl-??-methyldihydrocinnamic alcohol, which is subsequently dehydrogenated to the desired aldehyde. 4-tert-Butyl-??-methyldihydrocinnamaldehyde is more stable than cyclamenaldehyde and is a popular component of flower compositions, particularly lily of the valley and linden types, because of its mild, pleasant, blossomfragrance. It is used in a wide range of perfume types, but especially in soap and detergent perfumes.

You can find Lily aldehyde suppliers, manufacturers, and distributors from countries such as China, United States and the India here. Browse to the tetrahydrofuran product information displayed by the supplier, as well as the supplier's contact and capability information.