beta,2,2,3-tetramethyl-delta-methylene-3-cyclopentene-1-butanol
firsantol (Firmenich)
 
Notes:
None found
  • Azelis UK
    • Azelis UK Ltd.
      Chemical Distribution
      Azelis is a leading global distributor of speciality chemicals.
      Azelis is a leading global speciality chemicals distributor. We provide a diverse range of products and innovative services to more than 20,000 customers. Our in-depth local knowledge is supported by an international structure and value-added services including high levels of technical support and tailored solutions.
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      Email: Gaynor Cowan
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      Product(s):
      942596 FIRSANTOL™
       
  • Firmenich
    • Firmenich Inc.
      We Create
      We create perfumes and flavors for the World's most desirable brands.
      Firmenich is the largest privately-owned company in the perfume and flavor business. Swiss and family owned, we have created many of the world’s favorite perfumes for over 100 years and produced a number of the most well known flavors we enjoy each day.
      US Email: Fred Keifer
      US Voice: +1 609 452 1000
      US Fax: +1 609 452 6077
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      Product(s):
      942596 FIRSANTOL® for fragrance
      FIRSANTOL™ can be used in any type of fragrances to give a powerful sandalwood touch. Tenacity is improved with a very natural sandalwood aspect.
       
       
  • Ernesto Ventós
  • Vigon International
    • Vigon International
      Passion for Simplicity
      Manufacturer and supplier of high quality flavor and fragrance ingredients.
      The growth and success of Vigon is due in large part to a unique corporate concept that Vigon has developed and established within the industry: Creative Partnerships. This partnership concept has been and continues to be the foundation and guiding principle for all of Vigon's activities.
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      Products List: View
      Product(s):
      504845 Firsantol
       
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Fragrance Demo Formulas
CAS Number: 104864-90-6Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web: J2.470.888H
XlogP3-AA: 3.70 (est)
Molecular Weight: 208.34448000
Formula: C14 H24 O
NMR Predictor: Predict (works with chrome, Edge or firefox)
Category: fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Perfumer and Flavorist: Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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Physical Properties:
Appearance: colorless clear liquid (est)
Assay: 93.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 295.28 °C. @ 760.00 mm Hg (est)
Flash Point: 227.00 °F. TCC ( 108.10 °C. ) (est)
logP (o/w): 4.430
Soluble in:
 alcohol
 water, 5.204 mg/L @ 25 °C (est)
Stability:
 APC: 0.1 - 1%
 candle: 0.1 - 5%
 detergent: 0.1 - 5%
 fine fragrances: 0.1 - 5%
 shampoo: 0.1 - 1%
 shower gel: 0.1 - 1%
 soap: 0.1 - 1%
 softener: 0.1 - 5%
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Organoleptic Properties:
 
Odor Type: woody
 
Odor Strength: high ,
recommend smelling in a 10.00 % solution or less
 
Substantivity: 336 hour(s) at 100.00 %
 
 natural  sandalwood  
Odor Description:
at 10.00 % in dipropylene glycol. 
natural sandalwood
 
Odor and/or flavor descriptions from others (if found).
 
Firmenich
FIRSANTOL® for fragrance
Odor Description: Very powerful and natural sandalwood note
FIRSANTOL™ can be used in any type of fragrances to give a powerful sandalwood touch. Tenacity is improved with a very natural sandalwood aspect.
 
 
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Cosmetic Information:
None found
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Suppliers:
Azelis UK
FIRSANTOL™
Ernesto Ventós
FIRSANTOL FIRMENICH
Odor: WOODY, SANDALWOOD
Firmenich
FIRSANTOL®
for fragrance
Odor: Very powerful and natural sandalwood note
Use: FIRSANTOL™ can be used in any type of fragrances to give a powerful sandalwood touch. Tenacity is improved with a very natural sandalwood aspect.
Perfumery Laboratory
FIRSANTOL® Firmenich
Odor: Creamy, woody fragrance of white sandalwood
Vigon International
Firsantol
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Safety Information:
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
 
Recommendation for beta,2,2,3-tetramethyl-delta-methylene-3-cyclopentene-1-butanol flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 104864-90-6
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 16063533
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 2
 2-methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)pent-4-en-1-ol
Chemidplus: 0104864906
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References:
Leffingwell: Chirality or Article
 2-methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)pent-4-en-1-ol
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 16063533
Pubchem (sid): 135316263
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
HMDB (The Human Metabolome Database): Search
ChemSpider: View
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Potential Blenders and core components note
 
For Odor
amber
 acetoxymethyl isolongifoleneFR
 muscomerFR
balsamic
 amyris wood oilFL/FR
 amyris wood oil replacerFR
 brachyleana hutchinsii wood oilFR
 copaiba balsam oilFL/FR
 copaiba balsam oil replacerFR
creamy
 veratraldehydeFL/FR
floral
 geranium nitrileFR
fruity
 methyl (Z)-5-octenoateFL/FR
musk
 amyris specialtyFR
soapy
 soapy sandalwood moss fragranceFR
spicy
 zingeroneFL/FR
woody
 agarwood oilFR
 agarwood oil CO2 extractFR
 amyris acetateFR
 amyris bark oilFL/FR
 cedarwood oil replacerFR
 cedarwood oil terpenesFL/FR
 cedarwood oil whiteFR
alpha-cedrene epoxideFR
2-decalinyl formateFR
alpha-ethyl-2,2,6-trimethyl cyclohexane propanolFR
 indisan (IFF)FR
 melozol acetateFR
 methyl sandalFR
 sandal butenolFR
 sandal cyclohexanolFR
 sandal cyclopentaneFR
 sandal cyclopropaneFL/FR
 sandal glycol acetalFR
(R)-sandal hexanolFR
 sandal hexanolFR
 sandal octanolFR
 sandal pentanolFR
 sandal pentenolFL/FR
 sandal pentenoneFR
 sandalromeFR
 sandalwood essenceFL/FR
 sandalwood fragranceFR
 sandalwood oilFL/FR
 sandalwood oil CO2 extractFL/FR
 sandalwood oil replacerFR
 sandalwood oil west australiaFL/FR
 sandalwood oil west australia (santalum spicatum)FR
 sandalwood resinoidFL/FR
 sandalwood specialtyFR
 sandelFR
 sandelaFR
 santal penten-2-olFR
 santallFR
 santalolFL/FR
 santalum album extractFR
 santalum album wood extractFR
 santalum paniculatum wood oilFR
 santalyl acetateFL/FR
(+)-alpha-santalyl acetateFL/FR
 santalyl phenyl acetateFL/FR
 santol pentenolFR
 timber propanolFR
 vetiver oil acetylatedFR
 vetiverolFL/FR
 vetiveryl acetateFL/FR
 vetiveryl formateFR
 woody epoxideFR
 
For Flavor
 
No flavor group found for these
 amyris bark oilFL/FR
 sandal pentenolFL/FR
 sandalwood oil west australiaFL/FR
 santalolFL/FR
(+)-alpha-santalyl acetateFL/FR
 santalyl phenyl acetateFL/FR
 vetiveryl acetateFL/FR
amber
 sandal cyclopropaneFL/FR
balsamic
 copaiba balsam oilFL/FR
creamy
 veratraldehydeFL/FR
dairy
 methyl (Z)-5-octenoateFL/FR
spicy
 zingeroneFL/FR
woody
 amyris wood oilFL/FR
 cedarwood oil terpenesFL/FR
 sandalwood essenceFL/FR
 sandalwood oilFL/FR
 sandalwood oil CO2 extractFL/FR
 sandalwood resinoidFL/FR
 santalyl acetateFL/FR
 vetiverolFL/FR
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
3-cyclopentene-1-butanol, b,2,2,3-tetramethyl-d-methylene-
3-cyclopentene-1-butanol, beta,2,2,3-tetramethyl-delta-methylene-
 firsantol (Firmenich)
2-methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)pent-4-en-1-ol
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