jasmin pyranol
jasmelia (IFF)
Notes:
Jasmin absolute replacer.
  • Azelis
    • Azelis UK Life Sciences
      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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      Product(s):
      JESSEMAL
       
  • Indukern F&F
  • Liaison Carbone
    • Liaison Carbone
      Unusual Raw Materials
      Expanding the pallet of avid amateur-perfumers.
      This website is the result of my own attempts at getting hold of aroma chemicals that were hard to come by. At least in the amounts required by hobbyists. My goal is to offer an ever-changing portfolio of fairly unusual raw materials in order to continuously expand the pallet of avid amateur-perfumers.
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      JASMELIA
       
  • Taytonn
    • TAYTONN PTE LTD
      Supplying Asia Pacific
      We fully understand the demands of the F&F industry and we endeavour to supply quality products, with ready availability and a personalised service.
      Since 2001 TAYTONN has been distributing key ingredients to the Fragrance and Flavor industry in Asia. We work closely with customers, principals and vendors. Together we forecast demand and match it with supply of aroma chemicals, essential oils and natural isolates & extracts. Sourced from around the world, our F&F ingredient inventory in Singapore is ready to ship to any location in Asia and beyond. Time and again, we help our principals introduce new discoveries to the F&F market - stimulating creativity and bringing value added proposition to our customers.
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      Jasmelia
       
  • The John D. Walsh Company
    • The John D. Walsh Company, Inc
      Suppliers Since 1942
      Supplying the fragrance and flavor industry with high quality products.
      The John D. Walsh Company, Inc. has evolved from its beginnings as an agent/broker into a distributor of essential oils, aroma chemicals, concretes and absolutes. We currently represent the following companies, as their North American distributor: Destilerias Munoz Galvez, S.A. International Flavors & Fragrances PFW Aroma Chemicals B.V. Innospec Widnes Limited Hydrodiffusion de Guatemala, S. A. DSM Nutritional Products The John D. Walsh Company, Inc. is proud to be a founding member of IFEAT, an active member of IFRA, North America, and a corporate sponsor of the WFFC.
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      History
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      Jessemal®
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Synonyms   Articles   Notes   Search
(3-butyl-5-methyloxan-4-yl) acetate (Click)
CAS Number: 38285-49-3
ECHA EINECS - REACH Pre-Reg: 253-863-2
Nikkaji Web: J53.895G
XlogP3-AA: 2.80 (est)
Molecular Weight: 214.30494000
Formula: C12 H22 O3
NMR Predictor: Predict (works with chrome 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
IBM Patents: Obtain
Pubchem Patents: Search
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Physical Properties:
Appearance: colorless clear liquid (est)
Assay: 90.00 to 100.00 % sum of isomers
Food Chemicals Codex Listed: No
Specific Gravity: 0.96500 to 0.97300 @  25.00 °C.
Pounds per Gallon - (est).: 8.030 to  8.096
Specific Gravity: 0.96600 to 0.97400 @  20.00 °C.
Pounds per Gallon - est.: 8.047 to 8.114
Refractive Index: 1.44700 to 1.45200 @  20.00 °C.
Boiling Point: 271.00 to  272.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.006000 mm/Hg @ 25.00 °C. (est)
Flash Point: 212.00 °F. TCC ( 100.00 °C. )
logP (o/w): 3.010 (est)
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Organoleptic Properties:
Odor Type: floral
Odor Strength: medium
 floral  jasmin  parsley  spicy  
Odor Description:
at 100.00 %. 
floral jasmin jasmone parsley jasmin absolute
Substantivity: 356 Hour(s)
  
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
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Suppliers:
Azelis
JESSEMAL
Services
Creatingperfume.com
Jessemal (IFF)
Ernesto Ventós
JESSEMAL IFF
Odor: LACTONE, JASMIN, MUSHROOM
IFF
Jasmelia
Odor: Strong Jasmone odor with a hint of parsley which gives a jasmin absolute connotation
Indukern F&F
JESSEMAL
Odor: JASMIN, FLORAL
CROP CALENDAR
Liaison Carbone
JASMELIA
Moellhausen
JESSEMAL
Artificial
Taytonn
Jasmelia
Odor: Floral, Green, Parsley
The John D. Walsh Company
Jessemal®
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Safety Information:
European information :
Most important hazard(s):
Xi - Irritant
R 36/38 - Irritating to skin and eyes.
S 02 - Keep out of the reach of children.
S 24/25 - Avoid contact with skin and eyes.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 36 - Wear suitable protective clothing.
 
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:
oral-rat LD50  > 5000 mg/kg
Food and Cosmetics Toxicology. Vol. 14, Pg. 601, 1976.

Dermal Toxicity:
skin-rabbit LD50 > 5000 mg/kg
Food and Cosmetics Toxicology. Vol. 14, Pg. 601, 1976.

Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: fragrance agents
Recommendation for jasmin pyranol usage levels up to:
  10.0000 % in the fragrance concentrate.
 
Recommendation for jasmin pyranol flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
EPA Substance Registry Services (TSCA): 38285-49-3
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 161960
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 2
 (3-butyl-5-methyloxan-4-yl) acetate
Chemidplus: 0038285493
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References:
Leffingwell: chirality
 (3-butyl-5-methyloxan-4-yl) acetate
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 38285-49-3
Pubchem (cid): 161960
Pubchem (sid): 135117822
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Other Information:
(IUPAC): Atomic Weights of the Elements 2009
(IUPAC): Atomic Weights of the Elements 2009 (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
Export Tariff Code: 2915.39.9050
ChemSpider: View
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Potential Blenders and core components note
green algae absoluteFL/FR
 allyl amyl glycolateFR
 amber carbinolFR
isoamyl benzoateFL/FR
alpha-amyl cinnamaldehydeFL/FR
isoamyl salicylateFL/FR
 amyris wood oilFL/FR
para-anisyl acetateFL/FR
para-anisyl alcoholFL/FR
 beeswax absoluteFL/FR
 benzyl acetateFL/FR
 benzyl alcoholFL/FR
 benzyl benzoateFL/FR
 benzyl cinnamateFL/FR
 benzyl propionateFL/FR
 benzyl salicylateFL/FR
 bergamot oil bergaptene reduced italyFL/FR
 bois de rose oil brazilFL/FR
isobutyl benzoateFL/FR
isobutyl cinnamateFL/FR
isobutyl salicylateFL/FR
 carum carvi fruit oilFL/FR
 daucus carota fruit oilFL/FR
 cinnamyl alcoholFL/FR
 citronellolFL/FR
 citronellyl acetateFL/FR
 clary sage oil franceFL/FR
 clove bud oilFL/FR
 clover nitrileFR
 coconut absoluteFL/FR
 coriander seed oilFL/FR
 costus valerolactoneFR
para-cresyl caprylateFL/FR
black currant bud absoluteFL/FR
 cyclamen aldehydeFL/FR
 cyclohexyl ethyl alcoholFL/FR
(E)-alpha-damasconeFL/FR
(E)-beta-damasconeFL/FR
gamma-decalactoneFL/FR
 decanal (aldehyde C-10)FL/FR
 decanolFL/FR
 dihydrojasmoneFL/FR
 dimethyl anthranilateFL/FR
 dimethyl benzyl carbinyl acetateFL/FR
 dimethyl benzyl carbinyl butyrateFL/FR
para-dimethyl hydroquinoneFL/FR
 diphenyl oxideFL/FR
 ethyl cinnamateFL/FR
 ethyl phenyl acetateFL/FR
 eugenolFL/FR
isoeugenyl acetateFL/FR
 fir balsam absoluteFR
 floral pyranolFR
 gardenia oxideFR
 geraniolFL/FR
 geranyl acetateFL/FR
(E)-geranyl acetoneFL/FR
 grapefruit pentanolFR
 green acetateFR
 heliotropinFL/FR
 heliotropyl acetoneFL/FR
 heliotropyl diethyl acetalFR
gamma-heptalactoneFL/FR
gamma-hexalactoneFL/FR
(Z)-3-hexen-1-yl acetateFL/FR
(Z)-3-hexen-1-yl benzoateFL/FR
(Z)-3-hexen-1-yl butyrateFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
(Z)-3-hexen-1-yl tiglateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 hexyl tiglateFL/FR
 ho leaf oilFR
 hyacinth etherFR
 hydroxycitronellalFL/FR
 indoleFL/FR
 jasmin absolute egypt (from concrete)FL/FR
 lavender absolute bulgariaFL/FR
 leerallFR
 linaloolFL/FR
laevo-linaloolFL/FR
 linalool oxideFL/FR
 linalyl acetateFL/FR
 methyl (E)-cinnamateFL/FR
 methyl anthranilateFL/FR
 methyl dihydrojasmonateFL/FR
 methyl isoeugenolFL/FR
 mimosa absolute franceFL/FR
 muguet carboxaldehydeFR
beta-naphthyl ethyl etherFL/FR
 nerolFL/FR
 nerolidolFL/FR
 neryl acetateFL/FR
gamma-nonalactone (aldehyde C-18 (so-called))FL/FR
 nonanal (aldehyde C-9)FL/FR
 nonanolFL/FR
 oakmoss absoluteFL/FR
 ocean propanalFL/FR
 orris pyridine 25% IPMFR
 patchouli ethanoneFR
 peony alcoholFR
 phenethyl alcoholFL/FR
 phenethyl phenyl acetateFL/FR
 phenyl acetaldehyde dimethyl acetalFL/FR
3-phenyl propionaldehydeFL/FR
3-phenyl propyl alcoholFL/FR
 raspberry ketoneFL/FR
 raspberry ketone acetateFL/FR
 raspberry ketone methyl etherFL/FR
 rhodinolFL/FR
 rose butanoateFL/FR
 santallFR
 strawberry furanoneFL/FR
 strawberry glycidate 1 (aldehyde C-16 (so-called))FL/FR
alpha-terpineolFL/FR
 tetrahydrolinaloolFL/FR
 tobacarol (IFF)FR
 tonka bean absoluteFR
gamma-undecalactone (aldehyde C-14 (so-called))FL/FR
10-undecenal (aldehyde C-11 undecylenic)FL/FR
 vanilla bean absolute (vanilla planifolia)FL/FR
 veramoss (IFF)FR
 violet leaf absoluteFL/FR
 violet methyl carbonateFR
 watermelon ketoneFR
 woody acetateFR
(Z)-woody amyleneFR
 ylang ylang flower oilFL/FR
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Potential Uses:
 amberFR
 apricotFR
 balsamFR
 bergamotFR
 celeryFL/FR
 citrusFR
 floralFR
 freshener 
 fruitFR
 herbalFR
 honey mielFR
 jasminFR
 jonquil narcissus jonquillaFR
 mapleFR
 mintFR
 neroliFR
 orange blossomFR
 parsleyFL/FR
 peachFR
 peppermintFR
 raspberryFR
 spearmintFR
 spiceFR
 tea 
 tobaccoFR
 tomato 
 tuberoseFR
 waxy 
 woodyFR
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Natural Occurrence in: note
 not found in nature
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Synonyms:
3-butyl tetrahydro-5-methyl-2H-pyran-4-yl acetate
(3-butyl-5-methyloxan-4-yl) acetate
 jasmelia (IFF)
 jasmin pyranol
 jasmine pyranol
 jessemal
5-methyl-3-butyl tetrahydropyran-4-yl acetate
2H-pyran-4-ol, 3-butyl tetrahydro-5-methyl acetate
 tepyl acetate
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Articles:
 None found yet.
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click on the picture(s) below to
interact with the 3D model
Picture of molecule
Soluble in:
 alcohol
 water, 67.78 mg/L @ 25 °C (est)
Insoluble in:
 water
Stability:
 alcoholic lotion
 antiperspirant
 deo stick
 detergent
 fabric softener
 hard surface cleaner
 shampoo
 soap
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