Allyl Anthranilate

CAS: 7493-63-2

HeartFloral
Identifiers
Manufacturer
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CAS number
7493-63-2
CAS (all sources)
7493-63-2
CAS (Perfumiarz)
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CAS (PerfumersWorld)
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CAS (FraterWork)
7493-63-2
CAS (EU Hekserij)
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CAS (TSCA Hekserij)
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INCI name (FraterWork)
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IUPAC name (FraterWork)
prop-2-enyl 2-aminobenzoate
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)
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Scent profile
Note type (FraterWork)
Heart Note
Odour family (FraterWork)
Floral
Odour profile (FraterWork)
Allyl Anthranilate has a sharp, penetrating green-leaf aroma with floral-grape undertones, a bitter almond-like allyl bite, and a surprisingly creamy heliotropin drydown.
Longevity (FraterWork)
Lasts > 40 hours on a smelling strip.
Appearance (FraterWork)
Clear Liquid
Descriptions
Comment (FraterWork)
This is not your sweet fruit methyl anthranilate — it is the scary big brother! Allyl Anthranilate greets you with sharp, penetrating green-leaf intensity — far removed from the soft grape of its cousin Methyl Anthranilate. A bitter, almost almond-like bite cuts through immediately, metallic and arresting. Beneath that aggression hides unexpected floral warmth and heliotropin-like creaminess. This is a modifier, not a standalone note. Trace additions bring realistic grape-skin astringency to fruity accords that would otherwise read as candy. It sharpens galbanum and violet leaf with metallic green bite, adding modern edge to compositions that feel too soft or botanical. Dilute Allyl Anthranilate before evaluating — the neat material is overwhelmingly chemical. The creamy grape drydown only reveals itself at working concentrations. Blend with methyl anthranilate, heliotropin, and indole for narcissus accords, or with galbanum for sharp green-floral metalwork. Like Methyl Anthranilate, Allyl Anthranilate is a primary amine and will form Schiff bases with aldehydes, resulting in increased substantivity and characteristic deepening of color. Out of interest, Allyl-Aurantiol (Hydroxycitronellal and Allyl Anthranilate) is more radiant than classic Aurantiol (Hydroxycitronellal and Methyl Anthranilate). aromachem Best Seller NEW
Notes
This is not your sweet fruit methyl anthranilate — it is the scary big brother! Allyl Anthranilate greets you with sharp, penetrating green-leaf intensity — far removed from the soft grape of its cousin Methyl Anthranilate. A bitter, almost almond-like bite cuts through immediately, metallic and arresting. Beneath that aggression hides unexpected floral warmth and heliotropin-like creaminess. This is a modifier, not a standalone note. Trace additions bring realistic grape-skin astringency to fruity accords that would otherwise read as candy. It sharpens galbanum and violet leaf with metallic green bite, adding modern edge to compositions that feel too soft or botanical. Dilute Allyl Anthranilate before evaluating — the neat material is overwhelmingly chemical. The creamy grape drydown only reveals itself at working concentrations. Blend with methyl anthranilate, heliotropin, and indole for narcissus accords, or with galbanum for sharp green-floral metalwork. Like Methyl Anthranilate, Allyl Anthranilate is a primary amine and will form Schiff bases with aldehydes, resulting in increased substantivity and characteristic deepening of color. Out of interest, Allyl-Aurantiol (Hydroxycitronellal and Allyl Anthranilate) is more radiant than classic Aurantiol (Hydroxycitronellal and Methyl Anthranilate). aromachem Best Seller NEW
Usage
Uses (FraterWork)
Penetrating green-floral modifier adding grape astringency to narcissus, green, and fruity accords. IUPAC Name: prop-2-enyl 2-aminobenzoate
IFRA 51 (FraterWork)
No restriction for category 4 Odour Family: Floral Appearance: Clear Liquid Longevity: Lasts > 40 hours on a smelling strip. Odour Profile: Allyl Anthranilate has a sharp, penetrating green-leaf aroma with floral-grape undertones, a bitter almond-like allyl bite, and a surprisingly creamy heliotropin drydown. Uses: Penetrating green-floral modifier adding grape astringency to narcissus, green, and fruity accords. IUPAC Name: prop-2-enyl 2-aminobenzoate

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