ethyl vanillate
vanillic acid, ethyl ester
 
Notes:
Flavouring compound [Flavornet]
  • BOC Sciences
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      BOC Sciences is a brand of BOCSCI Inc. We leverage our wide spectrum of business in the fields of development, manufacturing, marketing, and distribution to help you make best-informed decisions tailored to your evolving needs for premium chemicals. Our complete suite of CRO services spans the entire molecule development pipeline including contract research for target identification, building blocks, compound synthesis, biochemical and cellular analysis, preclinical animal tests, and clinical studies.
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      Product(s):
      617-05-0 Vanilicacidethylester; 97%
       
  • Penta International
    • Penta International Corporation
      Chemistry innovation
      At Penta, our products and services help businesses do business better.
      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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      Product(s):
      05-75100 ETHYL VANILLATE
       
  • Synerzine
    • Synerzine, Inc.
      Innovation. Customization. Aroma Ingredients.
      Synerzine is a leading supplier of flavor and fragrance ingredients.
      Synerzine expresses what we have grown to embody as an organization - the synergy and connection between raw ingredients, science, technology, and the final product. Our experienced team is passionate about bringing our customers high-quality innovative ingredients that they can trust.
      Building upon our 44 year history, the Synerzine team provides customers around the globe with convenient access to over 1200 high-quality aroma ingredients. We actively engage with customers to add a wide array of new products and services on a regular basis. Our aim is to delight every customer with our exceptional services, large product selection, customization and the highest quality and safety standards. We provide our customers with true value designed to help them bring their products to market faster.
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      Product(s):
      W0534 Ethyl Vanillate
       
  • TCI AMERICA
    • TCI AMERICA
      Moving Your Chemistry Forward
      We continuously strive to advance our technology.
      With East & West Coast distribution centers, count on TCI to deliver products quickly and reliably. Over 30,000 Reagents available today in benchtop to bulk quantities. We also offer custom synthesis solutions. Sign up for a TCI account today for fast and free shipping!
      Tokyo Chemical Industry Co., Ltd. (TCI) is a leading worldwide manufacturer of specialty organic chemicals founded in 1946. TCI provides organic laboratory chemicals as well as pharmaceutical, cosmetic and functional materials. More than 70 years of synthesis experience and multi-purpose plants enable TCI to offer more than 30,000 products as well as custom synthesis.
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      Product(s):
      V0051 Ethyl Vanillate >98.0%(GC)
      SDS
       
  • United International
    • Qingdao Free Trade Zone United International Co Ltd
      Quality Products
      A partner in your supply chain solution.
      Qingdao Free Trade Zone United International Trade Co., Ltd.was founded in 1996, specializing in the production and import and export of food additives,flavor raw materials and pharmaceutical and chemical raw materials. The company has experienced R&D and business personnel,product quality, low price, efficient service and fast insight and grasp the latest market information.
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      Product(s):
      7256 Ethyl Vanillate
       
Synonyms   Articles   Notes   Search
CAS Number: 617-05-0Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 210-503-9
FDA UNII: V38JK4Z93O
Nikkaji Web: J21.705K
Beilstein Number: 2100025
MDL: MFCD00017269
CoE Number: 2302
XlogP3: 2.10 (est)
Molecular Weight: 196.20244000
Formula: C10 H12 O4
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome, Edge or firefox)
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
DG SANTE Food Flavourings: 09.798  ethyl vanillate
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Physical Properties:
Appearance: white powder (est)
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Melting Point: 44.00 °C. @ 760.00 mm Hg
Boiling Point: 292.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.001000 mmHg @ 25.00 °C. (est)
Flash Point: 252.00 °F. TCC ( 122.22 °C. )
logP (o/w): 2.741 (est)
Soluble in:
 alcohol
 water, very slightly
 water, 484.5 mg/L @ 25 °C (est)
Insoluble in:
 water
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Organoleptic Properties:
 
Odor Type: phenolic
 
 phenolic  burnt  guaiacol  smoky  powdery  metallic  
Odor Description:
at 100.00 %. 
phenolic burnt guaiacol smoky powdery metallic
Luebke, William tgsc, (2006)
 
 
Flavor Type: creamy
 
 creamy  phenolic  spicy  guaiacol  woody burnt wood  powdery  vanilla  
Taste Description:
sweet creamy phenolic spicy guaiacol burnt wood powdery vanilla
Luebke, William tgsc, (2006)
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
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Suppliers:
BOC Sciences
For experimental / research use only.
Vanilicacidethylester; 97%
Coompo
For experimental / research use only.
Ethyl Vanillate from Plants ≥98%
Inoue Perfumery
ETHYL VANILLATE
Kingchem Laboratories
ETHYL VANILLATE
Odor: Warm floral, phenolic, long lasting
Penta International
ETHYL VANILLATE
Santa Cruz Biotechnology
For experimental / research use only.
Ethyl 4-hydroxy-3-methoxybenzoate
Shijiazhuang Donglian Nankai Aroma Chemicals
Ethyl Vanillate
Odor: Burnt coffee
Sigma-Aldrich
For experimental / research use only.
Ethyl Vanillate analytical reference material
Synerzine
Ethyl Vanillate
TCI AMERICA
For experimental / research use only.
Ethyl Vanillate >98.0%(GC)
United International
Ethyl Vanillate
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Safety Information:
Preferred SDS: View
 
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:
intravenous-mouse LD50  56 mg/kg
U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#06395

oral-rabbit LDLo  3000 mg/kg
"Handbook of Toxicology," 4 vols., Philadelphia, W.B. Saunders Co., 1956-59Vol. 1, Pg. 138, 1955.

Dermal Toxicity:
subcutaneous-rat LD50 2000 mg/kg
"Handbook of Toxicology," 4 vols., Philadelphia, W.B. Saunders Co., 1956-59Vol. 1, Pg. 138, 1955.

Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: flavor and 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 ethyl vanillate usage levels up to:
  1.0000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.024 (μg/capita/day)
Modified Theoretical Added Maximum Daily Intake (mTAMDI): 3900 (μg/person/day)
Threshold of Concern:1800 (μg/person/day)
Structure Class: I
 
Food categories according to Commission Regulation EC No. 1565/2000 (EC, 2000) in FGE.06 (EFSA, 2002a). According to the Industry the "normal" use is defined as the average of reported usages and "maximum use" is defined as the 95th percentile of reported usages (EFSA, 2002i).
Note: mg/kg = 0.001/1000 = 0.000001 = 1/1000000 = ppm.
 average usage mg/kgmaximum usage mg/kg
Dairy products, excluding products of category 02.0 (01.0): 7.0000035.00000
Fats and oils, and fat emulsions (type water-in-oil) (02.0): 5.0000025.00000
Edible ices, including sherbet and sorbet (03.0): 10.0000050.00000
Processed fruit (04.1): 7.0000035.00000
Processed vegetables (incl. mushrooms & fungi, roots & tubers, pulses and legumes), and nuts & seeds (04.2): --
Confectionery (05.0): 10.0000050.00000
Chewing gum (05.0): --
Cereals and cereal products, incl. flours & starches from roots & tubers, pulses & legumes, excluding bakery (06.0): 5.0000025.00000
Bakery wares (07.0): 10.0000050.00000
Meat and meat products, including poultry and game (08.0): 2.0000010.00000
Fish and fish products, including molluscs, crustaceans and echinoderms (MCE) (09.0): 2.0000010.00000
Eggs and egg products (10.0): --
Sweeteners, including honey (11.0): --
Salts, spices, soups, sauces, salads, protein products, etc. (12.0): 5.0000025.00000
Foodstuffs intended for particular nutritional uses (13.0): 10.0000050.00000
Non-alcoholic ("soft") beverages, excl. dairy products (14.1): 5.0000025.00000
Alcoholic beverages, incl. alcohol-free and low-alcoholic counterparts (14.2): 10.0000050.00000
Ready-to-eat savouries (15.0): 20.00000100.00000
Composite foods (e.g. casseroles, meat pies, mincemeat) - foods that could not be placed in categories 01.0 - 15.0 (16.0): 5.0000025.00000
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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) on a request from the Commission related to Flavouring Group Evaluation 20 (FGE.20): Benzyl alcohols, benzaldehydes, a related acetal, benzoic acids, and related esters from chemical group 23
View page or View pdf
Flavouring Group Evaluation 52 (FGE.52): Consideration of hydroxy- and alkoxy-substituted benzyl derivatives evaluated by JECFA (57th meeting) structurally related to benzyl alcohols, benzaldehydes, a related acetal, benzoic acids, and related esters evaluated by EFSA in FGE.20 (2005) (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 54 (FGE.54)[1] - Consideration of benzyl derivatives evaluated by JECFA (57th meeting) structurally related to benzyl alcohols, benzaldehydes, a related acetal, benzoic acids and related esters evaluated by EFSA in FGE.20 (2005) - 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 20, Revision 1 (FGE.20Rev1): Benzyl alcohols, benzaldehydes, a related acetal, benzoic acids and related esters from chemical group 23
View page or View pdf
Flavouring Group Evaluation 54, Revision 1 (FGE.54Rev1): Consideration of benzyl derivatives evaluated by JECFA (57th meeting) structurally related to benzyl alcohols, benzaldehydes, a related acetal, benzoic acids and related esters evaluated by EFSA in FGE.20Rev1 (2009)
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 20, Revision 2 (FGE.20Rev2): Benzyl alcohols, benzaldehydes, a related acetal, benzoic acids, and related esters from chemical groups 23 and 30
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 20, Revision 3(FGE.20Rev3): Benzyl alcohols, benzaldehydes, a related acetal, benzoic acids, and related esters from chemical groups 23 and 30
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 20, Revision 4 (FGE.20Rev4): Benzyl alcohols, benzaldehydes, a related acetal, benzoic acids, and related esters from chemical groups 23 and 30
View page or View pdf
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 617-05-0
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 12038
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 ethyl 4-hydroxy-3-methoxybenzoate
Chemidplus: 0000617050
RTECS: YW5425000 for cas# 617-05-0
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References:
 ethyl 4-hydroxy-3-methoxybenzoate
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 617-05-0
Pubchem (cid): 12038
Pubchem (sid): 134978064
Flavornet: 617-05-0
Pherobase: View
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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
FooDB: FDB029772
YMDB (Yeast Metabolome Database): YMDB01691
Export Tariff Code: 2918.99.5000
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
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Potential Blenders and core components note
 
For Odor
acidic
 cyclohexyl acetic acidFL/FR
amber
 ambrette seed oilFL/FR
anisic
para-acetanisoleFL/FR
ortho-acetanisoleFL/FR
ortho-anisaldehydeFL/FR
para-anisaldehydeFL/FR
balsamic
 benzophenoneFR
isobutyl benzoateFL/FR
 cinnamyl alcoholFL/FR
 ethyl cinnamateFL/FR
 guaiacyl phenyl acetateFL/FR
 peru balsam oilFL/FR
bready
 furfuralFL/FR
chocolate
 cocoa pentenalFL/FR
 vanillyl ethyl etherFL/FR
coffee
 furfuryl mercaptanFL/FR
coumarinic
 phthalideFL/FR
creamy
para-vanillic acidFL/FR
floral
para-anisaldehyde / methyl anthranilate schiff's baseFR
 anisyl propanal / methyl anthranilate schiff's baseFR
 dimethyl alpha-iononeFR
 dimethyl anthranilateFL/FR
 geranyl phenyl acetateFL/FR
 heliotropinFL/FR
 heliotropyl acetateFL/FR
(E)-beta-iononeFL/FR
alpha-ironeFL/FR
ortho-methyl acetophenoneFL/FR
beta-isomethyl iononeFL/FR
alpha-isomethyl ionone (50% min.)FL/FR
alpha-isomethyl ionone (90% min.)FL/FR
 methyl ionyl acetateFL/FR
 orris rhizome resinoid (iris pallida)FL/FR
isopropyl phenyl acetateFL/FR
 rhodinolFL/FR
 rhodinyl phenyl acetateFL/FR
(E)-2,5,9-trimethyl-4,9-decadien-1-alFR
fruity
 acetyl methyl anthranilateFL/FR
 cherry oxyacetateFL/FR
 ethyl 3-hydroxyhexanoateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
 peach pivalateFR
 tolualdehydes (mixed o,m,p)FL/FR
green
3,7-dimethyl-6-octenoic acidFL/FR
para-methyl hydratropaldehydeFL/FR
 phenoxyethyl isobutyrateFL/FR
 safranalFL/FR
leathery
 castoreum absoluteFL/FR
musk
 cyclohexadecanoneFR
 ethylene brassylateFL/FR
 exaltone (Firmenich)FR
dextro,laevo-musconeFL/FR
 musk amberolFR
 musk indaneFR
 musk tetralinFL/FR
omega-pentadecalactoneFL/FR
musty
 cocoa butenalFL/FR
naphthyl
para-methyl anisoleFL/FR
beta-naphthyl ethyl etherFL/FR
nutty
2,3,5-trimethyl pyrazineFL/FR
phenolic
2,3-dimethyl benzofuranFL/FR
para-alpha-dimethyl styreneFL/FR
ortho-guaiacolFL/FR
4-methyl-2,6-dimethoxyphenolFL/FR
 piper betle leaf oilFR
2-propyl phenolFL/FR
2,5-xylenolFL/FR
powdery
para-anisyl acetateFL/FR
para-anisyl alcoholFL/FR
alpha-methyl iononeFL/FR
 birch tar oilFL/FR
 cade oilFR
2,6-dimethoxyphenolFL/FR
alpha-ethoxy-ortho-cresolFL/FR
4-ethyl phenolFL/FR
 phoebe oil brazil 
 propyl parabenCS
 pyroligneous acidsFL/FR
 pyroligneous acids hickoryFL/FR
 cubeb oilFL/FR
4-ethyl guaiacolFL/FR
 eugenolFL/FR
isoeugenyl acetateFL/FR
 pepper tree berry oilFL/FR
tobacco
 methyl benzoxoleFL/FR
vanilla
 heliotropyl alcoholFL/FR
 vanilla cresolFR
 vanillinFL/FR
 vanillin propylene glycol acetalFL/FR
 vanillyl acetateFL/FR
 vanillylidene acetoneFL/FR
woody
 amber formateFR
 cistus twig/leaf oilFL/FR
 guaiacwood oilFL/FR
 guaiacyl acetateFL/FR
 gurjun balsam oilFR
(+)-alpha-santalyl acetateFL/FR
 timber propanolFR
 vetiveryl acetateFL/FR
 woody epoxideFR
 
For Flavor
 
No flavor group found for these
 benzyl disulfideFL
 birch tar oilFL/FR
alpha-ethoxy-ortho-cresolFL/FR
 heliotropyl alcoholFL/FR
beta-isomethyl iononeFL/FR
1-methyl pyrroleFL
 phoebe oil brazil 
 prenyl mercaptanFL
2-propyl phenolFL/FR
(+)-alpha-santalyl acetateFL/FR
 vetiveryl acetateFL/FR
amber
 ambrette seed oilFL/FR
 musk tetralinFL/FR
anisic
para-acetanisoleFL/FR
ortho-anisaldehydeFL/FR
ortho-methyl acetophenoneFL/FR
balsamic
 ethyl cinnamateFL/FR
 peru balsam oilFL/FR
 vanillylidene acetoneFL/FR
brown
 furfuralFL/FR
chemical
2,3-dimethyl benzofuranFL/FR
cherry
 heliotropinFL/FR
coconut
6-methyl coumarinFL
coffee
 furfuryl mercaptanFL/FR
coumarinic
 phthalideFL/FR
creamy
para-anisaldehydeFL/FR
para-vanillic acidFL/FR
floral
 cocoa pentenalFL/FR
3,7-dimethyl-6-octenoic acidFL/FR
 geranyl phenyl acetateFL/FR
 heliotropyl acetateFL/FR
pseudoiononeFL
alpha-isomethyl ionone (50% min.)FL/FR
alpha-isomethyl ionone (90% min.)FL/FR
 orris rhizome resinoid (iris pallida)FL/FR
 rhodinolFL/FR
fruity
 acetyl methyl anthranilateFL/FR
para-anisyl acetateFL/FR
para-anisyl alcoholFL/FR
isobutyl benzoateFL/FR
 cherry oxyacetateFL/FR
 dimethyl anthranilateFL/FR
 ethyl 3-hydroxyhexanoateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
alpha-methyl iononeFL/FR
 tolualdehydes (mixed o,m,p)FL/FR
green
 cinnamyl alcoholFL/FR
 cocoa butenalFL/FR
para-methyl hydratropaldehydeFL/FR
 phenoxyethyl isobutyrateFL/FR
herbal
 celery seed oleoresinFL
honey
isopropyl phenyl acetateFL/FR
leathery
 castoreum absoluteFL/FR
meaty
4-allyl-2,6-dimethoxyphenolFL
ortho-thioguaiacolFL
medicinal
2,6-dimethoxyphenolFL/FR
musk
 ethylene brassylateFL/FR
dextro,laevo-musconeFL/FR
musty
2-ethoxythiazoleFL
2,3,5-trimethyl pyrazineFL/FR
2,5-xylenolFL/FR
naphthyl
para-methyl anisoleFL/FR
nutty
 methyl benzoxoleFL/FR
onion
2-methyl-1,3-dithiolaneFL
phenolic
 guaiacyl phenyl acetateFL/FR
4-methyl-2,6-dimethoxyphenolFL/FR
powdery
ortho-acetanisoleFL/FR
beta-naphthyl ethyl etherFL/FR
 powdery ketoneFL
rummy
 vanillyl ethyl etherFL/FR
smoky
4-ethyl phenolFL/FR
 pyroligneous acidsFL/FR
 pyroligneous acids hickoryFL/FR
dextro-xyloseFL
spicy
 chipotle chili oleoresinFL
 cubeb oilFL/FR
para-alpha-dimethyl styreneFL/FR
 eugenolFL/FR
isoeugenyl acetateFL/FR
 pepper tree berry oilFL/FR
sweet
 cyclohexyl acetic acidFL/FR
vanilla
omega-pentadecalactoneFL/FR
 vanillinFL/FR
 vanillin propylene glycol acetalFL/FR
 vanillyl acetateFL/FR
waxy
 rhodinyl phenyl acetateFL/FR
woody
 cistus twig/leaf oilFL/FR
4-ethyl guaiacolFL/FR
ortho-guaiacolFL/FR
 guaiacwood oilFL/FR
 guaiacyl acetateFL/FR
(E)-beta-iononeFL/FR
alpha-ironeFL/FR
 methyl ionyl acetateFL/FR
 safranalFL/FR
 
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Potential Uses:
 ambrette oil replacerFR
 azaleaFR
 baby powderFR
 benzoin absolute replacerFL/FR
 betelFR
 heliotropeFR
 hugoniaFR
 marshmallowFL
 medical 
 peru balsamFR
 powderFR
 rose white roseFR
 vanillaFR
 yerba mateFL/FR
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Occurrence (nature, food, other): note
 rum - 0.3 mg/kg
Search  PMC Picture
 sake
Search  PMC Picture
 wine red wine - up to 113 mg/kg
Search  Picture
 wine white wine
Search  Picture
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Synonyms:
m-anisic acid, 4-hydroxy-, ethyl ester
 benzoic acid, 4-hydroxy-3-methoxy-, ethyl ester
 ethyl 4-hydroxy-3-methoxybenzoate
 ethyl-4-hydroxy-3-methoxybenzolcarboxylat
4-hydroxy-3-methoxybenzoic acid ethyl ester
4-hydroxy-m-anisic acid ethyl ester
4-hydroxy-meta-anisic acid ethyl ester
3-methoxy-4-hydroxybenzoic acid ethyl ester
3-methoxy-4-hydroxybenzoic acid, ethyl ester
 vanillic acid ethyl ester
 vanillic acid, ethyl ester
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