Aromavault

Identifiers

Manufacturer

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CAS number

17627-44-0

CAS (all sources)

17627-44-0

CAS (Perfumiarz)

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CAS (PerfumersWorld)

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CAS (FraterWork)

17627-44-0

CAS (EU Hekserij)

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CAS (TSCA Hekserij)

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INCI name (FraterWork)

BISABOLENE

IUPAC name (FraterWork)

1-methyl-4-(6-methylhepta-2,5-dien-2-yl)cyclohexene

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)

Balsamic

Odour profile (FraterWork)

Alpha-Bisabolene presents a sophisticated warm balsamic character with distinctive spicy and woody facets, enhanced by sweet undertones and subtle citrus-floral nuances reminiscent of myrrh and opoponax resins.

Longevity (FraterWork)

Lasts > 48 hours on a smelling strip.

Appearance (FraterWork)

Colourless liquid

Descriptions

Comment (FraterWork)

Bisabolene opens with an immediate recognition factor—this is the warm, resinous sweetness you detect at the heart of genuine myrrh and opoponax absolutes. The material presents a remarkably complex profile that explains its pivotal role in recreating some of perfumery's most precious naturals. Beyond its primary balsamic-spicy character lies a sophisticated interplay of woody warmth, subtle citrus facets, and even delicate floral whispers that allow it to bridge multiple fragrance families with extraordinary grace. This material's true genius lies in its ability to recreate the authentic signatures of prohibitively expensive natural materials. Deploy bisabolene at 0.5-3% when reconstructing myrrh or opoponax accords—it provides the crucial molecular backbone these resins are built upon. More remarkably, it makes an important contribution to the recreation of oud, offering perfumers a lower cost pathway to this increasingly rare material. Its presence in natural bergamot and lemon oils explains why it adds such authentic depth to citrus reconstitutions, transforming flat synthetic citrus into living, breathing recreations. Use it as a fixative for neroli at 0.1-0.5% to anchor those fleeting orange blossom notes without masking their delicacy. aromachem Best Seller no_reg

Notes

Bisabolene opens with an immediate recognition factor—this is the warm, resinous sweetness you detect at the heart of genuine myrrh and opoponax absolutes. The material presents a remarkably complex profile that explains its pivotal role in recreating some of perfumery's most precious naturals. Beyond its primary balsamic-spicy character lies a sophisticated interplay of woody warmth, subtle citrus facets, and even delicate floral whispers that allow it to bridge multiple fragrance families with extraordinary grace. This material's true genius lies in its ability to recreate the authentic signatures of prohibitively expensive natural materials. Deploy bisabolene at 0.5-3% when reconstructing myrrh or opoponax accords—it provides the crucial molecular backbone these resins are built upon. More remarkably, it makes an important contribution to the recreation of oud, offering perfumers a lower cost pathway to this increasingly rare material. Its presence in natural bergamot and lemon oils explains why it adds such authentic depth to citrus reconstitutions, transforming flat synthetic citrus into living, breathing recreations. Use it as a fixative for neroli at 0.1-0.5% to anchor those fleeting orange blossom notes without masking their delicacy. aromachem Best Seller no_reg

Usage

Uses (FraterWork)

Oriental and opoponax compositions, woody accords, citrus reconstitutions, oud recreations, and as fixative for delicate florals.

IFRA 51 (FraterWork)

No restriction for category 4 Odour Family: Balsamic Appearance: Colourless liquid Longevity: Lasts > 48 hours on a smelling strip. Odour Profile: Alpha-Bisabolene presents a sophisticated warm balsamic character with distinctive spicy and woody facets, enhanced by sweet undertones and subtle citrus-floral nuances reminiscent of myrrh and opoponax resins. Uses: Oriental and opoponax compositions, woody accords, citrus reconstitutions, oud recreations, and as fixative for delicate florals. INCI Name: BISABOLENE IUPAC Name: 1-methyl-4-(6-methylhepta-2,5-dien-2-yl)cyclohexene

Links

FraterWorkhttps://fraterworks.com/products/bisabolene

Bisabolene

Comments