Cis-3-Hexenyl Tiglate
CAS: 67883-79-8
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Identifiers
Manufacturer
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CAS number
67883-79-8
CAS (all sources)
67883-79-8
CAS (Perfumiarz)
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CAS (PerfumersWorld)
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CAS (FraterWork)
67883-79-8
CAS (EU Hekserij)
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CAS (TSCA Hekserij)
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INCI name (FraterWork)
CIS-3-HEXENYL TIGLATE
IUPAC name (FraterWork)
(Z)-hex-3-en-1-yl (E)-2-methylbut-2-enoate
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)
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Synonyms (FraterWork)
Leaf Acetate
Scent profile
Note type (FraterWork)
Top Note
Odour family (FraterWork)
Green
Odour profile (FraterWork)
Cis-3-hexenyl acetate presents an intensely sharp, green, and
diffusive aroma reminiscent of freshly cut grass, complemented by distinctive
fruity facets suggesting unripe banana peel, crisp green apple, and pear.
Longevity (FraterWork)
Lasts < 4 hours on a smelling strip.
Appearance (FraterWork)
Colourless liquid
Descriptions
Comment (FraterWork)
Cis-3-Hexenyl Tiglate opens with distinctive warm green character that
immediately sets it apart from typical leaf alcohol esters. This unique material
captures fresh-cut mushroom earthiness - not mouldy but clean and vegetal -
combined with unexpected banana-melon fruitiness. The subtle gardenia-chamomile
floralcy adds sophisticated depth that transforms simple green accords into
complex botanical stories.
You'll find Cis-3-Hexenyl Tiglate invaluable for adding naturalistic warmth to
green compositions that feel too sharp or synthetic. Use at 0.5-5% where its
earthy-herbaceous character provides the missing link between bright green top
notes and heavier base materials. Found naturally in honeysuckle flowers and
comprising 1.34% of gardenia headspace, it's essential for authentic white
floral reconstructions requiring green warmth.
The material excels in fougère compositions where its mushroom-earth facets
enhance lavender's herbal character while adding modern complexity. Combine with
lavender for enhanced naturalness, gardenia bases for authentic headspace
effects, or violet leaf for sophisticated green depth. Its unusual banana-melon
fruitiness bridges green and tropical territories brilliantly.
THE TIGLATE SIGNATURE
Tiglates possess a distinctive warm, slightly spicy-sweet character inherited
from tiglic acid that sets them apart from common acetates or propionates. While
simple esters like cis-3-hexenyl acetate deliver straightforward fresh-cut
grass, tiglates add unexpected warmth and complexity - think of the difference
between cold salad greens versus herbs warmed by the sun. This warmth manifests
as earthy-mushroom notes in hexenyl tiglate, rose-honey in phenethyl tiglate, or
minty coolness in isopropyl tiglate. The branched structure of tiglic acid
creates more persistent, complex esters that feel more natural and less
synthetic than their straight-chain counterparts.
aromachem Best Seller
Notes
Cis-3-Hexenyl Tiglate opens with distinctive warm green character that
immediately sets it apart from typical leaf alcohol esters. This unique material
captures fresh-cut mushroom earthiness - not mouldy but clean and vegetal -
combined with unexpected banana-melon fruitiness. The subtle gardenia-chamomile
floralcy adds sophisticated depth that transforms simple green accords into
complex botanical stories.
You'll find Cis-3-Hexenyl Tiglate invaluable for adding naturalistic warmth to
green compositions that feel too sharp or synthetic. Use at 0.5-5% where its
earthy-herbaceous character provides the missing link between bright green top
notes and heavier base materials. Found naturally in honeysuckle flowers and
comprising 1.34% of gardenia headspace, it's essential for authentic white
floral reconstructions requiring green warmth.
The material excels in fougère compositions where its mushroom-earth facets
enhance lavender's herbal character while adding modern complexity. Combine with
lavender for enhanced naturalness, gardenia bases for authentic headspace
effects, or violet leaf for sophisticated green depth. Its unusual banana-melon
fruitiness bridges green and tropical territories brilliantly.
THE TIGLATE SIGNATURE
Tiglates possess a distinctive warm, slightly spicy-sweet character inherited
from tiglic acid that sets them apart from common acetates or propionates. While
simple esters like cis-3-hexenyl acetate deliver straightforward fresh-cut
grass, tiglates add unexpected warmth and complexity - think of the difference
between cold salad greens versus herbs warmed by the sun. This warmth manifests
as earthy-mushroom notes in hexenyl tiglate, rose-honey in phenethyl tiglate, or
minty coolness in isopropyl tiglate. The branched structure of tiglic acid
creates more persistent, complex esters that feel more natural and less
synthetic than their straight-chain counterparts.
aromachem Best Seller
Usage
Average use (FraterWork)
0.16% in a perfume compound
Uses (FraterWork)
Cis-3-Hexenyl Tiglate presents warm green-earthy character with
distinctive herbaceous-mushroom nuances, fruity banana-melon facets, and subtle
gardenia-chamomile floralcy.
IFRA 51 (FraterWork)
No restriction for category 4
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