Lilial

CAS: 80-54-6

Heart
Identifiers
Manufacturer
other
CAS number
80-54-6
CAS (all sources)
80-54-6
CAS (Perfumiarz)
80-54-6
CAS (PerfumersWorld)
80-54-6
CAS (FraterWork)
80-54-6
CAS (EU Hekserij)
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CAS (TSCA Hekserij)
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INCI name (FraterWork)
BUTYLPHENYL METHYLPROPIONAL
IUPAC name (FraterWork)
3-(4-tert-butylphenyl)-2-methylpropanal
INCI (Hekserij)
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EC number (Hekserij)
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FEMA (Hekserij)
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UN number
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Synonyms (PerfumersWorld)
p-tert.Butyl-alpha-methyldihydrocinnamic aldehyde :xalpha-Methyl-p-tert.butyldihydrocinnamaldehyde :alpha-Methyl-4-(1,1,-dimethylethyl)benzenepropanal : Florilys extra :Lilestralis : Lilial : Lilion : Lily aldehyde : Lysmeral : novafleur :Rhonaldehyde : Bucinal
Synonyms (FraterWork)
Lilestralia, Lysmeral, Lily Aldehyde
Scent profile
Note (Perfumiarz)
Middle Note
Note type (FraterWork)
Base Note
Odour profile (FraterWork)
Lilial delivers an intensely radiant lily-of-the-valley floral character with distinctive watery-green freshness, aldehydic cleanliness, and soft powdery-sweet undertones that define the classic muguet scent.
Longevity (FraterWork)
Lasts 236 hours on a smelling strip.
Odor life hours (PerfumersWorld)
72
Relative odor impact (PerfumersWorld)
80
Appearance (FraterWork)
Colourless liquid
Descriptions
Description
Lilial is fresh light green floral lily muguet lindenblossom aldehyde lilacmodern.
Odor description (Perfumiarz)
aspects A classic, fresh-floral molecule. Easier to use than Cyclamen Aldehyde. Longer-lasting than Hydroxycitronellal and more prominent in the heart note than Lyral. Occupies a similar olfactory territory to the aforementioned compounds.
Odour (PerfumersWorld)
fresh light green floral lily notes muguet lindenblossom
Description (PerfumersWorld)
Lilial is fresh light green floral lily muguet lindenblossom aldehyde lilacmodern.
Comment (FraterWork)
Lilial opens with crystalline lily-of-the-valley freshness, its aldehydic sparkle creating immediate lift and radiance. The watery-green transparency reads as morning dew on white petals. This legendary molecule (discovered in the 1960s by IFF) captures muguet's elusive character with extraordinary fidelity and power. Lilial transforms heavy florals into airy bouquets through its unique Schiff base formations. Combine it with hydroxycitronellal [https://fraterworks.com/products/hydroxycitronellal] for classic muguet or add traces to rose for aldehydic brilliance. Its metallic-clean edge cuts through oriental bases, adding transparency without sacrificing richness. The material's 236-hour substantivity means your compositions maintain fresh character throughout wear. Use it at 0.5-3% in fine fragrance for optimal impact without overwhelming delicacy. Its affinity for phenylethyl alcohol [https://fraterworks.com/products/phenyl-ethyl-alcohol], citronellol [https://fraterworks.com/products/citronellol-98], and hedione [https://fraterworks.com/products/hedione] creates synergies that amplify overall radiance. The variant we sell is a particularly fine “Extra” quality in the Fraterworks® Signature range. NOTE: Over time lilial may oxidise which appears in the form of white crystals or clumps (lysmerylic acid). Remaining liquid can still be used by the oxidised material should be discarded. Lilial may contain a touch of Tocopherol for protection, but storing this material at temperatures below 15°C (59°F) is still advisable. Regulatory: this is banned by the EU but is still permitted by IFRA to 1.4% of your finished product. aromachem Best Seller EU_BAN
Notes
Lilial opens with crystalline lily-of-the-valley freshness, its aldehydic sparkle creating immediate lift and radiance. The watery-green transparency reads as morning dew on white petals. This legendary molecule (discovered in the 1960s by IFF) captures muguet's elusive character with extraordinary fidelity and power. Lilial transforms heavy florals into airy bouquets through its unique Schiff base formations. Combine it with hydroxycitronellal [https://fraterworks.com/products/hydroxycitronellal] for classic muguet or add traces to rose for aldehydic brilliance. Its metallic-clean edge cuts through oriental bases, adding transparency without sacrificing richness. The material's 236-hour substantivity means your compositions maintain fresh character throughout wear. Use it at 0.5-3% in fine fragrance for optimal impact without overwhelming delicacy. Its affinity for phenylethyl alcohol [https://fraterworks.com/products/phenyl-ethyl-alcohol], citronellol [https://fraterworks.com/products/citronellol-98], and hedione [https://fraterworks.com/products/hedione] creates synergies that amplify overall radiance. The variant we sell is a particularly fine “Extra” quality in the Fraterworks® Signature range. NOTE: Over time lilial may oxidise which appears in the form of white crystals or clumps (lysmerylic acid). Remaining liquid can still be used by the oxidised material should be discarded. Lilial may contain a touch of Tocopherol for protection, but storing this material at temperatures below 15°C (59°F) is still advisable. Regulatory: this is banned by the EU but is still permitted by IFRA to 1.4% of your finished product. aromachem Best Seller EU_BAN
Usage
Perfume uses (PerfumersWorld)
Muguet Aldehyde Lilac Lindenblossom ModernNo FEMA Number * Relative Odor Impact 80 * Odor Life on a smelling strip 72 hrs
Average use (FraterWork)
3% in a perfume compound Appearance: Colourless liquid Longevity: Lasts 236 hours on a smelling strip. Odour Profile: Lilial delivers an intensely radiant lily-of-the-valley floral character with distinctive watery-green freshness, aldehydic cleanliness, and soft powdery-sweet undertones that define the classic muguet scent. Uses: Former cornerstone ingredient for lily-of-the-valley, white floral accords, and clean aldehydic compositions across all fragrance categories. INCI Name: BUTYLPHENYL METHYLPROPIONAL IUPAC Name: 3-(4-tert-butylphenyl)-2-methylpropanal
Uses (FraterWork)
Former cornerstone ingredient for lily-of-the-valley, white floral accords, and clean aldehydic compositions across all fragrance categories.
IFRA 51 (FraterWork)
1.4% in finished product (Cat. 4)

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