Isocyclocitral
CAS: 1335-66-6
TopGreen
Identifiers
Manufacturer
IFF
CAS number
1335-66-6
CAS (all sources)
1335-66-6
CAS (Perfumiarz)
1335-66-6
CAS (PerfumersWorld)
1335-66-6
CAS (FraterWork)
1335-66-6
CAS (EU Hekserij)
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CAS (TSCA Hekserij)
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INCI name (FraterWork)
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IUPAC name (FraterWork)
2,4,6-Trimethylcyclohex-3-ene-1-carbaldehyde
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)
3,5,6-Trimethyl-3-cyclohexen-1-carboxaldehyde :2,4,6-Trimethyl-4-cyclohexen-1-carboxaldehyde : symmertric iso Cyclocitral :meta iso Cyclocitral : iso Cyclocitral : SA761
Synonyms (FraterWork)
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Scent profile
Note (Perfumiarz)
Top note
Note type (FraterWork)
Heart Note
Odour family (FraterWork)
Green
Odour profile (FraterWork)
Isocyclocitral delivers an intensely powerful green foliage
character with wet earth nuances, sharp aldehydic lift, and the photorealistic
scent of a flower shop's humid atmosphere.
Longevity (FraterWork)
Lasts 16 hours on a smelling strip.
Odor life hours (PerfumersWorld)
3
Relative odor impact (PerfumersWorld)
250
Appearance (FraterWork)
Colourless liquid
Descriptions
Description
Isocyclocitral is sharp leafy-herbal citrusy eau-de-colognes fresh-topnotes.
Odor description (Perfumiarz)
earthy nuances
Isocyclocitral's fragrance pierces the air with a piercing and almost
suffocating greenness, reminiscent of crushed stems, fresh and damp leaves, as
well as the famous scent of a florist's shop.
Description (PerfumersWorld)
Isocyclocitral is sharp leafy-herbal citrusy eau-de-colognes fresh-topnotes.
Comment (FraterWork)
Isocyclocitral opens with a piercing, almost suffocating green-aldehydic blast
that transforms in dilution to reveal photorealistic wet earth and crushed
stems. This powerful modifier captures the complete flower shop experience -
sappy green foliage, damp soil, and that distinctive cool humidity. Its unique
marine-grassy duality revolutionised fresh fragrances in the 1980s.
You'll find Isocyclocitral indispensable for cutting through oakmoss sweetness
while lifting its top notes. Use sparingly at 0.1-3% where its impact is
profound - Bedoukian noted "unusual effects obtained by small quantities cannot
be achieved with other known synthetics." Its exceptional synergy with ionones
adds dewy freshness to powdery violets.
The material excels in creating specific effects: tomato leaf accords, hyacinth
compositions, and modernised pine notes for functional products. Combine with
Triplal for intensely diffusive aquatic-green effects. React with methyl
anthranilate to form woody-orange blossom Schiff bases for unique captive notes.
DIFFERENCE FROM CITRAL
Though citral and isocyclocitral contain identical atoms, their structural
arrangement creates entirely different olfactory profiles. Citral presents pure,
linear lemon character - the dominant note in lemongrass oil and citrus
compositions. Isocyclocitral delivers no citrus character whatsoever, instead
creating complex atmospheric greenness reminiscent of a florist's workspace:
crushed stems, humid air, wet earth, and that distinctive metallic coolness.
Where citral provides single-note brightness for hesperidic accords,
isocyclocitral builds multi-layered environmental effects. This structural
difference makes citral ideal for straightforward citrus freshness, while
isocyclocitral excels at creating naturalistic green atmospheres with remarkable
depth and complexity. The materials serve completely different creative purposes
despite their shared formula.
aromachem Best Seller green
Notes
Isocyclocitral opens with a piercing, almost suffocating green-aldehydic blast
that transforms in dilution to reveal photorealistic wet earth and crushed
stems. This powerful modifier captures the complete flower shop experience -
sappy green foliage, damp soil, and that distinctive cool humidity. Its unique
marine-grassy duality revolutionised fresh fragrances in the 1980s.
You'll find Isocyclocitral indispensable for cutting through oakmoss sweetness
while lifting its top notes. Use sparingly at 0.1-3% where its impact is
profound - Bedoukian noted "unusual effects obtained by small quantities cannot
be achieved with other known synthetics." Its exceptional synergy with ionones
adds dewy freshness to powdery violets.
The material excels in creating specific effects: tomato leaf accords, hyacinth
compositions, and modernised pine notes for functional products. Combine with
Triplal for intensely diffusive aquatic-green effects. React with methyl
anthranilate to form woody-orange blossom Schiff bases for unique captive notes.
DIFFERENCE FROM CITRAL
Though citral and isocyclocitral contain identical atoms, their structural
arrangement creates entirely different olfactory profiles. Citral presents pure,
linear lemon character - the dominant note in lemongrass oil and citrus
compositions. Isocyclocitral delivers no citrus character whatsoever, instead
creating complex atmospheric greenness reminiscent of a florist's workspace:
crushed stems, humid air, wet earth, and that distinctive metallic coolness.
Where citral provides single-note brightness for hesperidic accords,
isocyclocitral builds multi-layered environmental effects. This structural
difference makes citral ideal for straightforward citrus freshness, while
isocyclocitral excels at creating naturalistic green atmospheres with remarkable
depth and complexity. The materials serve completely different creative purposes
despite their shared formula.
aromachem Best Seller green
Usage
Average use (FraterWork)
0.25% in a perfume compound
Uses (FraterWork)
Fougère freshness, chypre modernisation, floral stem effects requiring
naturalistic green power.
IUPAC Name: 2,4,6-Trimethylcyclohex-3-ene-1-carbaldehyde
IFRA 51 (FraterWork)
3% in finished product (Cat. 4)
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