Category: flavor and fragrance agents
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Physical Properties:
Appearance: | colorless to pale yellow clear oily liquid to solid (est) |
Assay: | 98.00 to 100.00 %
|
Food Chemicals Codex Listed: | No |
Specific Gravity: | 1.12300 to 1.13000 @ 25.00 °C.
|
Pounds per Gallon - (est).: | 9.344 to 9.403
|
Refractive Index: | 1.53300 to 1.54400 @ 20.00 °C.
|
Melting Point: | 28.00 to 32.00 °C. @ 760.00 mm Hg
|
Boiling Point: | 205.00 to 206.00 °C. @ 760.00 mm Hg
|
Boiling Point: | 119.00 to 120.00 °C. @ 40.00 mm Hg
|
Vapor Pressure: | 0.179000 mmHg @ 25.00 °C. (est) |
Vapor Density: | 4.27 ( Air = 1 ) |
Flash Point: | 180.00 °F. TCC ( 82.22 °C. )
|
logP (o/w): | 1.320 |
Shelf Life: | 24.00 month(s) or longer if stored properly. |
Storage: | store in cool, dry place in tightly sealed containers, protected from heat and light. store under nitrogen. |
Storage: | store under nitrogen. |
Soluble in: |
| alcohol | | water, 7226 mg/L @ 25 °C (est) | | water, 1.87E+04 mg/L @ 15 °C (exp) |
Organoleptic Properties:
|
Odor Type: phenolic |
|
Odor Strength: | high , recommend smelling in a 1.00 % solution or less |
|
Substantivity: | 280 hour(s) at 100.00 % |
|
| phenolic smoky spicy vanilla woody |
Odor Description: at 1.00 % in dipropylene glycol. | phenolic smoke spice vanilla woody Luebke, William tgsc, (1996) |
|
| phenolic smoky spicy medicinal vanilla savory meaty woody |
Odor Description:
| Phenolic, smoky, spicy, medicinal, vanilla and savory meaty with a woody nuance Mosciano, Gerard P&F 22, No. 3, 47, (1997) |
|
|
Flavor Type: woody |
|
| woody phenolic bacon savory smoky medicinal |
Taste Description: at 2.00 ppm. | Woody, phenolic, bacon, savory, smoky and medicinal Mosciano, Gerard P&F 22, No. 3, 47, (1997) |
|
Odor and/or flavor descriptions from others (if found). |
|
Sigma-Aldrich |
Guaiacol, natural, ≥99%, FG |
Odor Description: | medicinal; smoky; woody |
|
Moellhausen |
GUAIACOL |
Odor Description: | aromatic, phenolic |
Taste Description: | phenolic, smoke, woody, bacon |
|
PerfumersWorld |
Guaiacol |
Odor Description: | aromatic phenolic burnt |
|
Pell Wall Perfumes |
Guaiacol |
Odor Description: | Warm, smoky, vanilla, phenolic, soft, woody. Very Powerful Arctander gives some indication of the uses: “This Phenolether is used in perfume compositions in very modest amounts for certain floral types, such as Cananga and YlangYlang, minute traces in Lilac, Narcissus, Lily, etc. It is also useful in Carnation, while somewhat higher proportions can be used in Spice complexes. It is accompanied by the usual draw-backs of simple Phenols – sensitivity to alkali, air, daylight, iron, etc.” |
|
|
Cosmetic Information:
Suppliers:
Advanced Biotech |
GUAIACOL NATURAL
98% min. Odor: Burnt, Smoky |
Alfrebro |
Guaiacol, Natural
Odor: Phenolic, Smoky, Spicy Medicinal, Vanilla and Savory, Meaty |
Ambles Nature et Chimie |
GUAIACOL NAT
|
Anhui Suzhou Jinli Aromatic Chemicals |
Guaiacol
Odor: phenol, Sauced |
Augustus Oils |
Guaiacol
|
Services |
Aurochemicals |
GUAIACOL, Natural
|
Axxence Aromatic |
GERANYL PROPIONATE Natural, Kosher
|
Sustainability |
Beijing Lys Chemicals |
Guaiacol (natural)
|
Beijing Lys Chemicals |
Guaiacol
|
Berjé |
Guaiacol Pure
|
Happening at Berje |
BOC Sciences |
For experimental / research use only. |
Guaiacol >98%
|
Diffusions Aromatiques |
GUAIACOL NATUREL
|
Diffusions Aromatiques |
GUAIACOL
|
EMD Millipore |
For experimental / research use only. |
2-Methoxyphenol
|
Ernesto Ventós |
GUAIACOL
Odor: PHENOLIC, SPICY, VANILLA, SMOKY |
Excellentia International |
Guaiacol Natural
|
Fleurchem |
guaiacol natural
|
Fleurchem |
guaiacol
|
Foreverest Resources |
Guaiacol 99.5%
Odor: rich sweet Use: Guaiacol is an oily yellow liquid with a penetrating odor, obtained by distilling wood tar or wood creosote. |
Fuzhou Farwell |
Guaiacol,Natural
|
Glentham Life Sciences |
Guaiacol
|
Global Essence |
Guaiacol Natural
|
H. Interdonati, Inc. |
Guaiacol Kosher
|
Featured Products |
Hermitage Oils |
Guaiacol Natural Isolate
Odor: characteristic Use: Arctander has this to say “Powerful smoke-like, somewhat medicinal odor, sweeter than the prototype phenolic odor … This Phenolether is used in perfume compositions in very modest amounts for certain floral types, such as Cananga and Ylang Ylang, minute traces in Lilac, Narcissus, Lily, etc. It is also useful in Carnation, while somewhat higher proportions can be used in Spice complexes.” |
Indukern F&F |
GUAIACOL NATURAL
Odor: POWERFUL, SMOKY, MEDICINAL |
Indukern F&F |
GUAYACOL
Odor: POWERFUL, SMOKY, MEDICINAL |
Jiangyin Healthway |
Natural Guaiacol
|
New functional food ingredients |
Jinan Enlighten Chemical Technology(Wutong Aroma ) |
Guaiacol, Kosherk
|
Kunshan Sainty |
Guaiacol, Natural
|
Lluch Essence |
GUAIACOL NATURAL
|
Lluch Essence |
GUAIACOL
|
M&U International |
Guaiacol, Kosher
|
M&U International |
Nat. Guaiacol, Kosher
|
Moellhausen |
GUAIACOL
Odor: aromatic, phenolic Flavor: phenolic, smoke, woody, bacon |
Natural Advantage |
Guaiacol Nat
Flavor: medical, smoky, sweet |
Riverside Aromatics LTD.is the exclusive distributor for Europe in UK for any non-US based inquiries |
Omega Ingredients |
Guaiacol Natural >99 %
|
Pell Wall Perfumes |
Guaiacol
Odor: Warm, smoky, vanilla, phenolic, soft, woody. Very Powerful Use: Arctander gives some indication of the uses: “This Phenolether is used in perfume compositions in very modest amounts for certain floral types, such as Cananga and YlangYlang, minute traces in Lilac, Narcissus, Lily, etc. It is also useful in Carnation, while somewhat higher proportions can be used in Spice complexes. It is accompanied by the usual draw-backs of simple Phenols – sensitivity to alkali, air, daylight, iron, etc.” |
Penta International |
GUAIACOL NATURAL
|
Penta International |
GUAIACOL
|
PerfumersWorld |
Guaiacol 10% in DPG
|
PerfumersWorld |
Guaiacol
Odor: aromatic phenolic burnt |
Reincke & Fichtner |
ortho-Guaiacol natural
|
Reincke & Fichtner |
ortho-Guaiacol
|
Riverside Aromatics |
GUAIACOL, NATURAL
|
Robertet |
GUAIACOL
Pure & Nat (EU) |
Santa Cruz Biotechnology |
For experimental / research use only. |
Guaiacol >98%
|
Sigma-Aldrich |
Guaiacol, natural, ≥99%, FG
Odor: medicinal; smoky; woody |
Certified Food Grade Products |
Sunaux International |
Guaiacol
|
Sunaux International |
nat.Guaiacol
|
Synerzine |
GUAIACOL, NATURAL
|
Synerzine |
Guaicol
|
TCI AMERICA |
For experimental / research use only. |
Guaiacol >98.0%(GC)
|
Tengzhou Xiang Yuan Aroma Chemicals |
Guaiacol
|
The Good Scents Company |
ortho-guaiacol
Odor: phenolic smoke spice vanilla woody |
The Lermond Company |
GUAIACOL
|
The Perfumers Apprentice |
Guaiacol 1% (PG)
Odor: phenolic smoke spice |
The Perfumers Apprentice |
Guaiacol
Odor: phenolic smoke spice |
United International |
Guaiacol Nat.
|
Vigon International |
Guaiacol 98%
Odor: PHENOL-LIKE |
Vigon International |
GUAIACOL NATURAL
|
WholeChem |
Guaiacol
|
Safety Information:
Preferred SDS: View |
European information : |
Most important hazard(s): | Xn - Harmful. |
R 22 - Harmful if swallowed. 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) |
Acute toxicity, Oral (Category 4), H302 Skin irritation (Category 2), H315 Eye irritation (Category 2A), H319 Acute aquatic toxicity (Category 3), H402 Chronic aquatic toxicity (Category 3), H412
|
GHS Label elements, including precautionary statements |
|
Pictogram | |
|
Signal word | Warning |
Hazard statement(s) |
H302 - Harmful if swallowed H315 - Causes skin irritation H319 - Causes serious eye irritation H402 - Harmful to aquatic life H412 - Harmful to aquatic life with long lasting effects
|
Precautionary statement(s) |
P264 - Wash skin thouroughly after handling. P270 - Do not eat, drink or smoke when using this product. P273 - Avoid release to the environment. P280 - Wear protective gloves/protective clothing/eye protection/face protection. P301 + P312 - IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell. P302 + P352 - IF ON SKIN: wash with plenty of soap and water. P305 + P351 + P338 - IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P330 - Rinse mouth. P332 + P313 - IF SKIN irritation occurs: Get medical advice/attention. P337 + P313 - IF eye irritation persists: Get medical advice/attention. P362 - Take off contaminated clothing and wash before reuse. P501 - Dispose of contents/ container to an approved waste disposal plant.
|
Oral/Parenteral Toxicity: |
oral-mouse LD50 621 mg/kg (Cioli et al., 1980)
gavage-rat LD50 [sex: M,F] 725 mg/kg (Taylor et al., 1964)
oral-cat LDLo 1500 mg/kg Food and Chemical Toxicology. Vol. 20, Pg. 697, 1982.
oral-human LDLo 43 mg/kg GASTROINTESTINAL: OTHER CHANGES
BEHAVIORAL: TREMOR "Toxicology of Drugs and Chemicals," Deichmann, W.B., New York, Academic Press, Inc., 1969Vol. -, Pg. 295, 1969.
intravenous-mouse LD50 170 mg/kg Food and Chemical Toxicology. Vol. 20, Pg. 697, 1982.
oral-mouse LD50 621 mg/kg Drugs of the Future. Vol. 5, Pg. 539, 1980.
intravenous-rabbit LDLo 3700 ug/kg Journal of Agricultural and Food Chemistry. Vol. 17, Pg. 497, 1969.
oral-rabbit LDLo 2000 mg/kg Food and Chemical Toxicology. Vol. 20, Pg. 697, 1982.
oral-rat LD50 520 mg/kg BEHAVIORAL: GENERAL ANESTHETIC Folia Medica Cracoviensia. Vol. 32, Pg. 309, 1991.
|
Dermal Toxicity: |
subcutaneous-guinea pig LDLo 900 mg/kg Food and Chemical Toxicology. Vol. 20, Pg. 697, 1982.
subcutaneous-rabbit LDLo 1250 mg/kg Food and Chemical Toxicology. Vol. 20, Pg. 697, 1982.
subcutaneous-rat LDLo 900 mg/kg Food and Chemical Toxicology. Vol. 20, Pg. 697, 1982.
|
Inhalation Toxicity: |
inhalation-mouse LC50 7570 mg/m3 Food and Chemical Toxicology. Vol. 20, Pg. 697, 1982.
|
Safety in Use Information:
Category: | flavor and fragrance agents |
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice |
Recommendation for ortho-guaiacol usage levels up to: | | 0.5000 % in the fragrance concentrate.
|
|
Maximised Survey-derived Daily Intakes (MSDI-EU): | 44.00 (μg/capita/day) |
Maximised Survey-derived Daily Intakes (MSDI-USA): | 16.00 (μg/capita/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. Update in publication number(s): 29 |
Click here to view publication 3 |
| average usual ppm | average maximum ppm |
baked goods: | 2.00000 | 3.00000 |
beverages(nonalcoholic): | 0.80000 | 1.00000 |
beverages(alcoholic): | 1.00000 | 15.00000 |
breakfast cereal: | - | - |
cheese: | 0.10000 | 0.10000 |
chewing gum: | 0.01000 | 0.01000 |
condiments / relishes: | - | - |
confectionery froastings: | - | - |
egg products: | - | - |
fats / oils: | - | - |
fish products: | - | - |
frozen dairy: | 0.70000 | 2.00000 |
fruit ices: | - | - |
gelatins / puddings: | 0.90000 | 2.00000 |
granulated sugar: | - | - |
gravies: | - | - |
hard candy: | 1.00000 | 1.00000 |
imitation dairy: | - | - |
instant coffee / tea: | - | - |
jams / jellies: | - | - |
meat products: | 3.00000 | 6.00000 |
milk products: | - | - |
nut products: | - | - |
other grains: | - | - |
poultry: | - | - |
processed fruits: | - | - |
processed vegetables: | - | - |
reconstituted vegetables: | - | - |
seasonings / flavors: | - | - |
snack foods: | - | - |
soft candy: | 0.80000 | 2.00000 |
soups: | - | - |
sugar substitutes: | - | - |
sweet sauces: | - | - |
Safety References:
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): |
Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) related to Flavouring Group Evaluation 22 (FGE.22): Ring-substituted phenolic substances from chemical groups 21 and 25 (Commission Regulation (EC) No 1565/2000 of 18 July 2000) View page or View pdf |
Flavouring Group Evaluation 58 (FGE.58) Consideration of phenol derivatives evaluated by JECFA (55th meeting) structurally related to ring substituted phenolic substances evaluated by EFSA in FGE.22 (2006) (Commission Regulation (EC) No 1565/2000 of 18 July 2000) - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC) View page or View pdf |
Flavouring Group Evaluation 60 (FGE.60): Consideration of eugenol and related hydroxyallylbenzene derivatives evaluated by JECFA (65th meeting) structurally related to ring- substituted phenolic substances evaluated by EFSA in FGE.22 (2006) View page or View pdf |
Scientific Opinion on Flavouring Group Evaluation 22, Revision 1 (FGE.22Rev1): Ring-substituted phenolic substances from chemical groups 21 and 25 View page or View pdf |
Scientific Opinion on the safety and efficacy of phenol derivatives containing ring-alkyl, ring-alkoxy and side-chains with an oxygenated functional group (chemical group 25) when used as flavourings for all species View page or View pdf |
Review of substances/agents that have direct beneficial effect on the environment: mode of action and assessment of efficacy View page or View pdf |
EPI System: | View |
ClinicalTrials.gov: | search |
Chemical Carcinogenesis Research Information System: | Search |
Cancer Citations: | Search |
Toxicology Citations: | Search |
EPA GENetic TOXicology: | Search |
EPA Substance Registry Services (TSCA): | 90-05-1 |
EPA ACToR: | Toxicology Data |
EPA Substance Registry Services (SRS): | Registry |
Laboratory Chemical Safety Summary : | 460 |
National Institute of Allergy and Infectious Diseases: | Data |
WGK Germany: | 1 |
| 2-methoxyphenol |
Chemidplus: | 0000090051 |
EPA/NOAA CAMEO: | hazardous materials |
RTECS: | SL7525000 for cas# 90-05-1 |
References:
Other Information:
Potential Blenders and core components note
|
For Odor |
aldehydic |
| dodecanal (aldehyde C-12 lauric) | FL/FR |
10- | undecenal (aldehyde C-11 undecylenic) | FL/FR |
amber |
| ambroxan | FL/FR |
| angelica root oil | FL/FR |
| cistus ladaniferus resinoid | FL/FR |
animal |
iso | butyl quinoline | FR |
iso | butyl quinoline | FR |
| costus valerolactone | FR |
para- | cresyl caprylate | FL/FR |
anise |
| anise seed oil colombia | FL/FR |
anisic |
para- | anisaldehyde | FL/FR |
| dihydroanethol | FL/FR |
balsamic |
| amyris wood oil | FL/FR |
siam | benzoin resinoid | FL/FR |
sumatra | benzoin resinoid | FL/FR |
| benzyl salicylate | FL/FR |
laevo- | bornyl acetate | FL/FR |
iso | bornyl acetate | FL/FR |
iso | butyl cinnamate | FL/FR |
| clover nitrile | FR |
| ethyl cinnamate | FL/FR |
| fir balsam absolute | FR |
| methyl cinnamate | FL/FR |
3- | phenyl propyl alcohol | FL/FR |
caramellic |
| cyclotene | FL/FR |
| immortelle absolute | FL/FR |
| maltol | FL/FR |
chocolate |
| vanillyl ethyl ether | FL/FR |
coconut |
gamma- | heptalactone | FL/FR |
gamma- | nonalactone (aldehyde C-18 (so-called)) | FL/FR |
gamma- | octalactone | FL/FR |
coffee |
| furfuryl mercaptan | FL/FR |
floral |
iso | amyl salicylate | FL/FR |
iso | butyl salicylate | FL/FR |
| heliotropin | FL/FR |
| heliotropyl acetone | FL/FR |
alpha- | hexyl cinnamaldehyde | FL/FR |
| orris pyridine 25% IPM | FR |
| phenethyl alcohol | FL/FR |
| phenethyl phenyl acetate | FL/FR |
fruity |
| ethyl 3-hydroxyhexanoate | FL/FR |
green |
para- | dimethyl hydroquinone | FL/FR |
3,7- | dimethyl-6-octenoic acid | FL/FR |
hay |
| hay absolute | FR |
herbal |
| ajowan seed oil | FL/FR |
| balsamite oil | |
| thyme absolute | FL/FR |
honey |
| methyl phenyl acetate | FL/FR |
leathery |
| castoreum absolute | FL/FR |
licorice |
(E)- | anethol | FL/FR |
medicinal |
2- | hydroxybenzaldehyde | FL/FR |
summer | savory oil | FL/FR |
mossy |
| oakmoss absolute | FL/FR |
| veramoss (IFF) | FR |
naphthyl |
2,4- | dimethyl benzaldehyde | FL/FR |
nutty |
| nutty cyclohexenone | FL/FR |
phenolic |
2,3- | dimethyl benzofuran | FL/FR |
para-alpha- | dimethyl styrene | FL/FR |
4- | methyl-2,6-dimethoxyphenol | FL/FR |
| piper betle leaf oil | FR |
2-iso | propyl phenol | FL/FR |
2- | propyl phenol | FL/FR |
2,5- | xylenol | FL/FR |
powdery |
para- | anisyl acetate | FL/FR |
| birch tar oil | FL/FR |
| cade oil | FR |
2,6- | dimethoxyphenol | FL/FR |
alpha- | ethoxy-ortho-cresol | FL/FR |
4- | ethyl phenol | FL/FR |
| phoebe oil brazil | |
| propyl paraben | CS |
| pyroligneous acids | FL/FR |
| pyroligneous acids hickory | FL/FR |
spicy |
| allspice berry oil | FL/FR |
| allspice oil | FL/FR |
| benzyl isoeugenol | FL/FR |
| cassia bark oil china | FL/FR |
| clove bud oil | FL/FR |
| cubeb oil | FL/FR |
4- | ethyl guaiacol | FL/FR |
iso | eugenol | FL/FR |
| eugenol | FL/FR |
iso | eugenyl acetate | FL/FR |
alpha- | methyl cinnamaldehyde | FL/FR |
| methyl isoeugenol | FL/FR |
| ocimum gratissimum herb oil india | FR |
| pepper tree berry oil | FL/FR |
| zingerone | FL/FR |
terpenic |
| frankincense oil | FL/FR |
(R)-(-)-alpha- | phellandrene | FL/FR |
tonka |
| coumarin | FR |
| tonka bean absolute | FR |
vanilla |
| ethyl vanillin | FL/FR |
| ethyl vanillin hexylene glycol acetal | FR |
| methyl vanillate | FL/FR |
| vanilla bean absolute (vanilla planifolia) | FL/FR |
| vanillyl acetate | FL/FR |
waxy |
| ethyl laurate | FL/FR |
woody |
| cistus twig/leaf oil | FL/FR |
| guaiacwood oil | FL/FR |
| guaiacyl acetate | FL/FR |
2- | methoxy-4-vinyl phenol | FL/FR |
| methyl cedryl ketone | FL/FR |
| patchouli ethanone | FR |
| patchouli oil | FL/FR |
4-iso | propyl phenol | FL/FR |
| santall | FR |
| tobacarol (IFF) | FR |
| woody acetate | FR |
(Z)- | woody amylene | FR |
| woody propanol | FR |
|
For Flavor |
|
No flavor group found for these |
| balsamite oil | |
| benzyl disulfide | FL |
| birch tar oil | FL/FR |
| cistus ladaniferus resinoid | FL/FR |
alpha- | ethoxy-ortho-cresol | FL/FR |
1- | methyl pyrrole | FL |
| methyl vanillate | FL/FR |
(R)-(-)-alpha- | phellandrene | FL/FR |
| phoebe oil brazil | |
| prenyl mercaptan | FL |
2- | propyl phenol | FL/FR |
animal |
para- | cresyl caprylate | FL/FR |
anise |
(E)- | anethol | FL/FR |
| anise seed oil colombia | FL/FR |
balsamic |
siam | benzoin resinoid | FL/FR |
sumatra | benzoin resinoid | FL/FR |
| benzyl salicylate | FL/FR |
laevo- | bornyl acetate | FL/FR |
iso | butyl cinnamate | FL/FR |
| ethyl cinnamate | FL/FR |
berry |
| heliotropyl acetone | FL/FR |
burnt |
4-iso | propyl phenol | FL/FR |
caramellic |
| cyclotene | FL/FR |
| maltol | FL/FR |
chemical |
2,3- | dimethyl benzofuran | FL/FR |
cherry |
| heliotropin | FL/FR |
coconut |
gamma- | nonalactone (aldehyde C-18 (so-called)) | FL/FR |
coffee |
| furfuryl mercaptan | FL/FR |
cooling |
iso | butyl salicylate | FL/FR |
creamy |
para- | anisaldehyde | FL/FR |
fatty |
10- | undecenal (aldehyde C-11 undecylenic) | FL/FR |
floral |
3,7- | dimethyl-6-octenoic acid | FL/FR |
| methyl phenyl acetate | FL/FR |
| phenethyl alcohol | FL/FR |
fruity |
para- | anisyl acetate | FL/FR |
| ethyl 3-hydroxyhexanoate | FL/FR |
green |
iso | amyl salicylate | FL/FR |
| angelica root oil | FL/FR |
para- | dimethyl hydroquinone | FL/FR |
| immortelle absolute | FL/FR |
| oakmoss absolute | FL/FR |
herbal |
| ajowan seed oil | FL/FR |
| dihydroanethol | FL/FR |
| thyme absolute | FL/FR |
honey |
| phenethyl phenyl acetate | FL/FR |
lactonic |
gamma- | heptalactone | FL/FR |
gamma- | octalactone | FL/FR |
leathery |
| castoreum absolute | FL/FR |
meaty |
4- | allyl-2,6-dimethoxyphenol | FL |
ortho- | thioguaiacol | FL |
medicinal |
2,6- | dimethoxyphenol | FL/FR |
summer | savory oil | FL/FR |
musty |
2,5- | xylenol | FL/FR |
naphthyl |
2,4- | dimethyl benzaldehyde | FL/FR |
nutty |
| nutty cyclohexenone | FL/FR |
onion |
2- | methyl-1,3-dithiolane | FL |
phenolic |
4- | methyl-2,6-dimethoxyphenol | FL/FR |
rummy |
| vanillyl ethyl ether | FL/FR |
smoky |
4- | ethyl phenol | FL/FR |
2- | methoxy-4-vinyl phenol | FL/FR |
| prosopis juliflora wood extract | FL |
| pyroligneous acids | FL/FR |
| pyroligneous acids hickory | FL/FR |
dextro- | xylose | FL |
soapy |
| dodecanal (aldehyde C-12 lauric) | FL/FR |
solvent |
2-iso | propyl phenol | FL/FR |
spicy |
| allspice berry oil | FL/FR |
| allspice oil | FL/FR |
| benzyl isoeugenol | FL/FR |
| cassia bark oil china | FL/FR |
| chipotle chili oleoresin | FL |
| clove bud oil | FL/FR |
| cubeb oil | FL/FR |
para-alpha- | dimethyl styrene | FL/FR |
| eugenol | FL/FR |
iso | eugenol | FL/FR |
iso | eugenyl acetate | FL/FR |
2- | hydroxybenzaldehyde | FL/FR |
alpha- | methyl cinnamaldehyde | FL/FR |
| methyl cinnamate | FL/FR |
| methyl isoeugenol | FL/FR |
| pepper tree berry oil | FL/FR |
3- | phenyl propyl alcohol | FL/FR |
winter | savory oil | FL |
| zingerone | FL/FR |
vanilla |
| ethyl vanillin | FL/FR |
| vanilla bean absolute (vanilla planifolia) | FL/FR |
| vanillyl acetate | FL/FR |
waxy |
| ethyl laurate | FL/FR |
alpha- | hexyl cinnamaldehyde | FL/FR |
woody |
| ambroxan | FL/FR |
| amyris wood oil | FL/FR |
iso | bornyl acetate | FL/FR |
| cistus twig/leaf oil | FL/FR |
4- | ethyl guaiacol | FL/FR |
| frankincense oil | FL/FR |
| guaiacwood oil | FL/FR |
| guaiacyl acetate | FL/FR |
| methyl cedryl ketone | FL/FR |
| patchouli oil | FL/FR |
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Potential Uses:
Occurrence (nature, food, other): note
Synonyms:
| anastil | | creodon | | guaiaco | | guaiacol | nat. | guaiacol | o- | guaiacol | o- | guaiacol natural | | guaiastil | | guajacol | | guajol | | guasol | 1- | hydroxy-2-methoxybenzene | 2- | hydroxy-anisole | 2- | hydroxyanisole | o- | hydroxyanisole | ortho- | hydroxyanisole | o- | methoxy catechol | 2- | methoxy-phenol | o- | methoxy-phenol | 1-oxy-2- | methoxybenzene | 2- | methoxyphenol | o- | methoxyphenol | ortho- | methoxyphenol | | methyl catechol | o- | methyl catechol | ortho- | methyl catechol | o- | methylcatechol | ortho- | methylcatechol | | phenol, 2-methoxy- | | pyrocatechol methyl ester | | pyrocatechol monomethyl ether |
Articles:
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