isobornyl formate
DL-isobornyl formate
 
Notes:
Flavouring agent
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      Product(s):
      1200-67-5 isoBornyl Formate
       
  • Penta International
    • Penta International Corporation
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      For over 30 years, Penta Manufacturing Company has played a growing role in worldwide chemistry innovations and applications. As an industry leader, Penta continues to pioneer chemistry-based solutions for practically every area of commerce. Our products and expertise have helped fuel technical advances in dozens of commercial applications including flavoring, coloring, fragrances and chemical processes.
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      09-35800 ISOBORNYL FORMATE
       
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CAS Number: 1200-67-5Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 214-853-3
FDA UNII: 8QPT973QF4
MDL: MFCD00135983
CoE Number: 565
XlogP3: 3.30 (est)
Molecular Weight: 182.26286000
Formula: C11 H18 O2
NMR Predictor: Predict (works with chrome or firefox)
EFSA/JECFA Comments: Racemate () = DL-Isobornyl formate (EFFA, 2010a). CASrn in Register refers to (1R,2R,4R)-rel. Register name to be changed to DL-Isobornyl formate (EFFA, 2011m). According to JECFA: Min. Assay value "may include small amounts of bornyl formate".
Category: flavor and 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
JECFA Food Flavoring: 1390  isobornyl formate
FLAVIS Number: 09.176 (Old)
DG SANTE Food Flavourings: 09.176  DL-isobornyl formate
FEMA Number: 2162  isobornyl formate
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):1200-67-5 ; ISOBORNYL FORMATE
FDA Regulation:
FDA PART 172 -- FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION
Subpart F--Flavoring Agents and Related Substances
Sec. 172.515 Synthetic flavoring substances and adjuvants.
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Physical Properties:
Appearance: colorless clear liquid (est)
Assay: 96.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 1.01100 to 1.01700 @  25.00 °C.
Pounds per Gallon - (est).: 8.413 to  8.462
Refractive Index: 1.46900 to 1.47300 @  20.00 °C.
Boiling Point: 110.00 °C. @ 20.00 mm Hg
Boiling Point: 85.00 to  86.00 °C. @ 7.00 mm Hg
Acid Value: 1.00 max. KOH/g
Vapor Pressure: 0.163000 mmHg @ 25.00 °C. (est)
Flash Point: 173.00 °F. TCC ( 78.33 °C. )
logP (o/w): 3.108 (est)
Soluble in:
 alcohol
 dipropylene glycol
 water, 80.06 mg/L @ 25 °C (est)
Insoluble in:
 water
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allyl formate
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3-hexen-1-yl formate
(Z)-3-hexen-1-yl formate
hexyl formate
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menthadienyl formate
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2-methyl butyl formate
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nonyl formate
nopyl formate
octyl formate
3-octyl formate
phenethyl formate
2-phenoxyethyl formate
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Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: balsamic
 
Odor Strength: medium
 
Substantivity: 12 hour(s) at 100.00 %
 
 camphoreous  musty  medicinal  woody  
Odor Description:
at 100.00 %. 
camphor musty medical woody
Luebke, William tgsc, (1985)
 
 cooling  musty  medicinal  camphoreous  minty  woody  earthy  
Odor Description:
Cooling, musty, medicinal, camphoreous, minty, with woody earthy nuances
Mosciano, Gerard P&F 16, No. 5, 71, (1991)
 
 
Flavor Type: woody
 
 woody  cooling  musty  floral  camphoreous  minty  
Taste Description:
at 30.00 ppm.  
Woody, cooling, musty, floral, camphoreous and minty
Mosciano, Gerard P&F 16, No. 5, 71, (1991)
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
BOC Sciences
For experimental / research use only.
isoBornyl Formate
Parchem
isoBornyl Formate
Penta International
ISOBORNYL FORMATE
Reincke & Fichtner
isoBornyl Formate
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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.
Human Experience:
2 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
oral-rat LD50  > 5000 mg/kg
(Levenstein, 1975p)

Dermal Toxicity:
skin-rabbit LD50 > 5000 mg/kg
(Levenstein, 1975p)

Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: flavor and fragrance agents
Recommendation for isobornyl formate usage levels up to:
  2.0000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.61 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 0.40 (μg/capita/day)
Threshold of Concern:1800 (μg/person/day)
Structure Class: I
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 3
Click here to view publication 3
 average usual ppmaverage maximum ppm
baked goods: -0.80000
beverages(nonalcoholic): 0.060001.00000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: 0.030001.00000
fruit ices: 0.030001.00000
gelatins / puddings: --
granulated sugar: --
gravies: --
hard candy: -0.74000
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: --
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: --
sugar substitutes: --
sweet sauces: --
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Safety References:
Flavor & Extract Manufacturers Association (FEMA) reference(s):
The FEMA GRAS assessment of alicyclic substances used as flavor ingredients. View pdf
European Food Safety Athority(efsa): Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...
European Food Safety Authority (EFSA) reference(s):
Flavouring Group Evaluation 47, (FGE.47)[1] - Bicyclic secondary alcohols, ketones and related esters from chemical group 8 - Scientific Opinion of the Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
View page or View pdf
Flavouring Group Evaluation 87, (FGE.87)[1] - Consideration of bicyclic secondary alcohols, ketones and related esters evaluated by JECFA (63rd meeting) structurally related to bicyclic secondary alcohols, ketones and related esters evaluated by EFSA in FGE.47 (2008) - Scientific Opinion of the Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 87 Revision 1 (FGE.87Rev1): Consideration of bicyclic secondary alcohols, ketones and related esters evaluated by JECFA (63rd meeting) structurally related to bicyclic secondary alcohols, ketones and related esters evaluated by EFSA in FGE.47 (2008)
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 87, Revision 2 (FGE.87Rev2): Consideration of bicyclic secondary alcohols, ketones and related esters evaluated by JECFA (63rd meeting) structurally related to bicyclic secondary alcohols, ketones and related esters evaluated by EFSA in FGE.47Rev1 (2008)
View page or View pdf
EPI System: View
EPA Substance Registry Services (TSCA): 1200-67-5
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 62387
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 2
 [(6S)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] formate
Chemidplus: 0001200675
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References:
 [(6S)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] formate
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 1200-67-5
Pubchem (cid): 62387
Pubchem (sid): 135020461
Flavornet: 1200-67-5
Pherobase: View
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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
FDA Substances Added to Food (formerly EAFUS): View
HMDB (The Human Metabolome Database): HMDB38245
FooDB: FDB017541
Export Tariff Code: 2915.13.0000
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
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Potential Blenders and core components note
 
For Odor
balsamic
dextro,laevo-borneolFL/FR
laevo-borneolFL/FR
isobornyl isobutyrateFL/FR
isobornyl methyl etherFL/FR
isobornyl propionateFL/FR
dextro-fenchoneFL/FR
 fir needle oil siberiaFL/FR
camphoreous
dextro-camphorFL/FR
beta-homocyclocitralFL/FR
 fencholFL/FR
laevo-fenchoneFL/FR
 herbal ethanoneFR
 melaleuca viridiflora leaf oilFR
 thujyl alcoholFL/FR
citrus
(E+Z)-4,8-dimethyl-3,7-nonadien-2-yl acetateFL/FR
 ocimene quintoxideFL/FR
coconut
3-butyl bicyclo[3.2.1]octan-2-oneFR
earthy
(-)-alpha-fencholFL/FR
 pogostemon cablin leaf extractFR
floral
 bois de rose oil terpenelessFL/FR
 dihydro-alpha-iononeFL/FR
 linalool oxideFL/FR
fruity
 geranyl acetoacetateFL/FR
1,3,3,5-tetramethyl-7 and 8-cyanobicyclo(2.2.2)octane 
green
isocyclocitral (IFF)FL/FR
 fern absolute 
 galbanum absoluteFL/FR
 galbanum oilFL/FR
 lawsonia inermis leaf oil CO2 extractFR
 oakmoss oilFR
herbal
1-allyl-2,2,7,7-tetramethyl cycloheptanolFR
 arnica flower absoluteFR
 barosma betulina leaf oilFL/FR
1,4-cineoleFL/FR
2-cyclohexyl cyclohexanoneFR
(Z)-isodihydrolavandulyl acetateFR
 eucalyptus globulus oilFL/FR
 geranic oxideFL/FR
 guava leaf oil cubaFR
 herbal dioxaneFR
 herbal undecanolFR
6-hydroxydihydrotheaspirane (mixture of isomers)FL/FR
 hyssop oilFL/FR
 methyl cyclogeranate (Firmenich)FR
 myrtenolFL/FR
 origanum oilFL/FR
 origanum oil greeceFL/FR
 pine hexanolFR
beta-pineneFL/FR
alpha-pineneFL/FR
 pinocarveolFL/FR
 piperitoneFL/FR
 rosemary absoluteFL/FR
 rosemary oil moroccoFL/FR
 rosemary oil spainFL/FR
 rosemary oleoresinFL/FR
 sabinene hydrateFL/FR
common tansy flower oilFR
common tansy flower oil dutchFR
 theaspiraneFL/FR
white thyme oilFL/FR
 thyme oil (thymus zygis gracillis) spainFL/FR
red thyme oil spainFL/FR
 thymolFL/FR
mentholic
laevo-mentholFL/FR
(±)-isomenthoneFL/FR
 peppermint cyclohexanoneFL/FR
minty
trans-para-menthan-2-oneFL/FR
5- and 6-isopropyl-1,3,3-trimethyl bicyclo(2.2.2)-5,7-octadien-2-one 
2,4,4,6-tetramethyl cyclohexa-2,5-diene-1-oneFR
mossy
 oakmoss absoluteFL/FR
musty
ketoisophoroneFL/FR
naphthyl
para-methyl anisoleFL/FR
1-methyl naphthaleneFL/FR
spicy
 carvacrolFL/FR
4-carvomenthenolFL/FR
 elettaria cardamomum seed oilFL/FR
 elettaria cardamomum seed oil guatemalaFL/FR
 ginger root oil chinaFL/FR
 piper matico leaf oil 
laevo-verbenoneFL/FR
terpenic
 cypress leaf oilFR
thujonic
 armoise oilFR
 cedarleaf oil terpenelessFR
common tansy oil canadaFR
tropical
 patchwoodFR
woody
2-tert-butyl cyclohexanoneFR
para-tert-butyl cyclohexanoneFR
(+)-campheneFL/FR
 cyperus root oil (cyperus scariosus)FR
 cypriol oil (cyperus scariosus)FR
 dihydro-beta-iononeFL/FR
 dihydro-gamma-iononeFL/FR
3(or 2),4-dimethyl-5-vinyl octahydro-4,7-methanoinden-5-ol 
 dryopteris filix-mas oleoresinFR
 germacrene B 
 herbal norbornaneFR
5,5a,6,7,8,8a-hexahydro-6,6,7,8,8-pentamethyl-4H-indeno[5,4-D]isoxazole 
 hinoki root oilFR
(-)-myrtenol 
 octahydro-3(or 2),4-dimethyl-4,7-methanoinden-5-one 
 orris hexanoneFR
 patchouli ethanolFR
 patchouli hexanolFR
terpeneless patchouli oilFL/FR
 patchouli oil chinaFL/FR
 pelargonium radula oilFR
 pinacolFR
 pogostemon cablin leaf oilFR
beta-terpineolFL/FR
1,3,3,5-tetramethyl-7 and 8-cyanobicyclo(2.2.2)oct-5-ene 
3(or 2),4,5-trimethyl octahydro-4,7-methanoinden-5-olFR
3(or 2),4,5-trimethyl-3a,4,5,6,7,7a-hexahydro-4,7-methanoinden-5-ol 
1,3,5,7-undecatetraeneFL/FR
 vetiver oil CO2 extractFL/FR
 vetiver oil fractionsFR
 vetiver oil haitiFL/FR
 vetiveria zizanioides root oilFL/FR
 
For Flavor
 
No flavor group found for these
dextro,laevo-borneolFL/FR
isobornyl methyl etherFL/FR
(+)-campheneFL/FR
 dihydro-gamma-iononeFL/FR
(E+Z)-4,8-dimethyl-3,7-nonadien-2-yl acetateFL/FR
3(or 2),4-dimethyl-5-vinyl octahydro-4,7-methanoinden-5-ol 
 fern absolute 
 germacrene B 
5,5a,6,7,8,8a-hexahydro-6,6,7,8,8-pentamethyl-4H-indeno[5,4-D]isoxazole 
3-methyl cyclohexanoneFL
 octahydro-3(or 2),4-dimethyl-4,7-methanoinden-5-one 
(Z,Z)-photocitral AFL
 piper matico leaf oil 
3-propyl pyridineFL
5- and 6-isopropyl-1,3,3-trimethyl bicyclo(2.2.2)-5,7-octadien-2-one 
beta-terpineolFL/FR
1,3,3,5-tetramethyl-7 and 8-cyanobicyclo(2.2.2)oct-5-ene 
1,3,3,5-tetramethyl-7 and 8-cyanobicyclo(2.2.2)octane 
3(or 2),4,5-trimethyl-3a,4,5,6,7,7a-hexahydro-4,7-methanoinden-5-ol 
1,3,5,7-undecatetraeneFL/FR
laevo-verbenoneFL/FR
 vitispiraneFL
 thujyl alcoholFL/FR
balsamic
isobornyl isobutyrateFL/FR
isobornyl propionateFL/FR
 fir needle oil siberiaFL/FR
berry
 dihydro-alpha-iononeFL/FR
camphoreous
laevo-borneolFL/FR
(-)-alpha-fencholFL/FR
 fencholFL/FR
laevo-fenchoneFL/FR
 geranic oxideFL/FR
6-hydroxydihydrotheaspirane (mixture of isomers)FL/FR
 pinocarveolFL/FR
citrus
ketoisophoroneFL/FR
cooling
4-carvomenthenolFL/FR
1,4-cineoleFL/FR
beta-homocyclocitralFL/FR
dextro-fenchoneFL/FR
laevo-mentholFL/FR
 sabinene hydrateFL/FR
 theaspiraneFL/FR
 WS-3FL
floral
 bois de rose oil terpenelessFL/FR
green
isocyclocitral (IFF)FL/FR
 galbanum absoluteFL/FR
 galbanum oilFL/FR
 linalool oxideFL/FR
 oakmoss absoluteFL/FR
 ocimene quintoxideFL/FR
isophoroneFL
herbal
 barosma betulina leaf oilFL/FR
 eucalyptus globulus oilFL/FR
 hyssop oilFL/FR
 origanum oilFL/FR
 origanum oil greeceFL/FR
 rosemary absoluteFL/FR
 rosemary oil moroccoFL/FR
 rosemary oil spainFL/FR
 rosemary oleoresinFL/FR
white thyme oilFL/FR
 thyme oil (thymus zygis gracillis) spainFL/FR
red thyme oil spainFL/FR
medicinal
dextro-camphorFL/FR
mentholic
 peppermint cyclohexanoneFL/FR
minty
trans-para-menthan-2-oneFL/FR
(±)-isomenthoneFL/FR
(-)-myrtenol 
 myrtenolFL/FR
 piperitoneFL/FR
musty
 geranyl acetoacetateFL/FR
naphthyl
para-methyl anisoleFL/FR
1-methyl naphthaleneFL/FR
phenolic
 thymolFL/FR
pine
beta-pineneFL/FR
spicy
 carvacrolFL/FR
 elettaria cardamomum seed oilFL/FR
 elettaria cardamomum seed oil guatemalaFL/FR
 ginger root oil chinaFL/FR
 turmeric oleoresinFL
woody
 dihydro-beta-iononeFL/FR
terpeneless patchouli oilFL/FR
 patchouli oil chinaFL/FR
alpha-pineneFL/FR
 vetiver oil CO2 extractFL/FR
 vetiver oil haitiFL/FR
 vetiveria zizanioides root oilFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 berryFR
 citrusFR
 coolingFL
 eucalyptus oil replacerFR
 fernFR
 fresh outdoorsFR
 gorse 
 heatherFR
 lavenderFR
 limeFR
 pineFR
 pinus palustris tarCS
 raspberryFR
 tweed 
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 anthemis coelopoda
Search Trop  Picture
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Synonyms:
 bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-, formate, (1R,2R,4R)-rel-
 bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-, formate, exo-
isoborneol formate
isoborneol, formate
DL-isobornyl formate
exo-2-bornyl formate
2-bornyl formate, exo-
isobornyl methanoate
exo-2-camphanyl formate
2-camphanyl formate, exo-
exo-1,7,7-trimethyl bicyclo(2.2.1)hept-2-yl formate
[(6S)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] formate
exo-1,7,7-trimethylbicyclo(2.2.1)hept-2-yl formate
1,7,7-trimethylbicyclo(2.2.1)heptan-2-yl formate, exo-
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