EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

ethyl formate
formic acid ethyl ester

Sponsors

Flavor Demo Formulas
Name:ethyl formate
CAS Number: 109-94-4Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:203-721-0
FDA UNII:0K3E2L5553
Nikkaji Web:J1.971B
Beilstein Number:0906769
MDL:MFCD00003294
CoE Number:339
XlogP3-AA:0.50 (est)
Molecular Weight:74.07922000
Formula:C3 H6 O2
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome 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
 FDA/DG SANTE Petitions, Reviews, Notices:
184.1295 Ethyl formate View-review
JECFA Food Flavoring:26 ethyl formate
FLAVIS Number:09.072 (Old)
DG SANTE Food Flavourings:09.072 ethyl formate
FEMA Number:2434 ethyl formate
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm: ETHYL FORMATE
FDA Regulation:
FDA PART 184 -- DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE
Subpart B--Listing of Specific Substances Affirmed as GRAS
Sec. 184.1295 Ethyl formate.
 
Physical Properties:
Appearance:colorless clear liquid (est)
Assay: 97.00 to 100.00
Food Chemicals Codex Listed: Yes
Specific Gravity:0.91600 to 0.92100 @ 25.00 °C.
Pounds per Gallon - (est).: 7.622 to 7.664
Refractive Index:1.35900 to 1.36300 @ 20.00 °C.
Melting Point: -81.00 to -80.00 °C. @ 760.00 mm Hg
Boiling Point: 52.00 to 54.00 °C. @ 760.00 mm Hg
Boiling Point: 6.00 to 7.00 °C. @ 100.00 mm Hg
Acid Value: 1.00 max. KOH/g
Vapor Pressure:245.000000 mm/Hg @ 25.00 °C.
Vapor Density:2.5 ( Air = 1 )
Flash Point: -3.00 °F. TCC ( -19.44 °C. )
logP (o/w): 0.230
Soluble in:
 alcohol
 fixed oils
 propylene glycol
 water, 8.511e+004 mg/L @ 25 °C (est)
Insoluble in:
 glycerin
 water
Similar Items:note
allyl formate
amyl formate
isoamyl formate
para-anisyl formate
benzyl formate
bornyl formate
isobornyl formate
butyl formate
isobutyl formate
sec-butyl formate
carvyl formate
cedryl formate
cinnamyl formate
citronellyl formate
para-cresyl formate
cyclododecyl formate
cyclohexyl formate
2-decalinyl formate
decyl formate
dimethyl benzyl carbinyl formate
eugenyl formate
isoeugenyl formate
furfuryl formate
S-furfuryl thioformate
geranyl formate
heptyl formate
(E)-2-hexen-1-yl formate
(E)-3-hexen-1-yl formate
3-hexen-1-yl formate
(Z)-3-hexen-1-yl formate
hexyl formate
linalyl formate
menthadienyl formate
menthyl formate
laevo-menthyl formate
2-methyl butyl formate
methyl formate
myrtenyl formate
neryl formate
nonisyl formate
nonyl formate
nopyl formate
octyl formate
3-octyl formate
phenethyl formate
2-phenoxyethyl formate
3-phenyl propyl formate
prenyl formate
propyl formate
isopropyl formate
isopulegyl formate
rhodinyl formate
styralyl formate
sulfuryl formate
terpinyl formate
 
Organoleptic Properties:
Odor Type: ethereal
Odor Strength:high ,
recommend smelling in a 1.00 % solution or less
Substantivity:4 hour(s) at 100.00 %
ethereal green alcoholic rose cognac
Odor Description:at 1.00 % in dipropylene glycol. ethereal green alcohol rose cognac
Luebke, William tgsc, (1989)
Odor sample from: Fritzsche Dodge & Olcott, Inc.
ethereal fermented winey cognac
Odor Description:at 2.00 %. Etherial, lifting, fermented, winey and cognac
Mosciano, Gerard P&F 23, No. 3, 55, (1998)
Flavor Type: ethereal
ethereal sweet grain fruity winey cognac
Taste Description: at 200.00 ppm. Etherial, sweet, grainy, fruity, winey and cognac
Mosciano, Gerard P&F 23, No. 3, 55, (1998)
Odor and/or flavor descriptions from others (if found).
Symrise
Ethyl formate
Odor Description:strong, ethereal-fruity, like rum
Taste Description:sweet, rum, fruity, baked fruit, whisky
Useful in: mint, savory vegetable, fruity red, fruity yellow, fruity tropical, fruity others, sweet others, alcoholics.
Moellhausen
ETHYL FORMATE
Odor Description:sweet, ethereal-fruity
Taste Description:sweet, fruity
Prodasynth
ETHYL FORMATE > 98
Odor Description:FRUITY, RUM, STRONG, ETHEREAL
Taste Description:SWEET,RUM,FRUITY,BAKED FRUIT,WHISKY
 
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: perfuming agents
 
Suppliers:
Advanced Biotech
ETHYL FORMATE NATURAL
90% min.
Odor: Fruity
Alfrebro
ETHYL FORMATE NATURAL
Odor: Sharp, Sweet, Ethereal, Rum
Aurochemicals
ETHYL FORMATE, Natural
Axxence Aromatic
ETHYL FORMATE Natural
Kosher
Sustainability
Berjé
Ethyl Formate
Happening at Berje
CG Herbals
Ethyl Formate
Odor: Pleasant ethereal-fruity and rum-like
Use: Ethyl Formate is used for its effect in floral compositions and as an additive to alcohol for perfumery use to give it "lift" and "aged" notes.
Flavor: characteristic
Ethyl Formate is very extensively used for imitating peach, pineapple, apple, apricot, banana, berry, butter, butterscotch, brandy, grape, plum, rum, sherry-wine, whisky, tutti-frutti, etc.
Charkit Chemical
ETHYL FORMATE FEMA 2434
Diffusions Aromatiques
FORMIATE ETHYLE
Ernesto Ventós
ETHYL FORMATE, NATURAL
Ernesto Ventós
ETHYL FORMATE
Odor: FRUITY, RUM, STRONG, ETHEREAL
Flavor: SWEET,RUM,FRUITY,BAKED FRUIT,WHISKY
Excellentia International
Ethyl Formate Natural
Fleurchem
ethyl formate natural
H. Interdonati, Inc.
Ethyl formate Natural, Kosher
Featured Products
Indenta Group
Ethyl Formate
Indukern F&F
ETHYL FORMATE
Kunshan Sainty
Ethyl Formate, Natural
Lluch Essence
ETHYL FORMATE NATURAL
Lluch Essence
ETHYL FORMATE
Odor: FRUITY, SWEET, ETHEREAL
M&U International
Ethyl Formate
M&U International
NAT.ETHYL FORMATE, Kosher
Moellhausen
ETHYL FORMATE
Odor: sweet, ethereal-fruity
Flavor: sweet, fruity
Nagar Haveli Perfumes & Aromatics
Ethyl Formate
Odor: Etherial, lifting, fermented, winey and cognac
Natural Advantage
Ethyl Formate Nat
Pearlchem Corporation
Natural Ethyl Formate
Penta International
ETHYL FORMATE FCC, Kosher
Penta International
ETHYL FORMATE, NATURAL, Kosher
Prodasynth
ETHYL FORMATE > 98
Odor: FRUITY, RUM, STRONG, ETHEREAL
Flavor: SWEET,RUM,FRUITY,BAKED FRUIT,WHISKY
Reincke & Fichtner
Ethyl Formate natural
Reincke & Fichtner
Ethyl Formate
Riverside Aromatics
ETHYL FORMATE, NATURAL
Robertet
Ethyl formate naturel
Santa Cruz Biotechnology
For experimental / research use only.
Ethyl Formate ≥97%
Sigma-Aldrich
Ethyl formate, ≥97%, FCC, FG
Odor: ethereal; fruity; sweet; wine-like
Certified Food Grade Products
Sigma-Aldrich
Ethyl formate, natural, ≥95%, FG
Odor: ethereal; fruity; sweet; wine-like
Silverline Chemicals
Ethyl Formate
Sunaux International
nat.Ethyl Formate
Symrise
Ethyl formate
Odor: strong, ethereal-fruity, like rum
Flavor: sweet, rum, fruity, baked fruit, whisky
Useful in: mint, savory vegetable, fruity red, fruity yellow, fruity tropical, fruity others, sweet others, alcoholics.
SysKem Chemie
Ethyl Formate
Taytonn
Ethyl Formate
Odor: Diffusive, Ethereal, Fruity, Warm
TCI AMERICA
For experimental / research use only.
Ethyl Formate [for Spectrophotometry] >98.0%(GC)
Treatt
Ethyl Formate
Ungerer & Company
Ethyl Formate
Vigon International
Ethyl Formate
Odor: Strong, ethereal-fruity, like rum
WEN International
ETHYL FORMATE Natural
 
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xn - Harmful.
R 11 - Highly flammable.
R 20/22 - Harmful by inhalation and if swallowed.
R 36/37 - Irritating to eyes and respiratory system.
S 09 - Keep container in a well-ventilated place.
S 16 - Keep away from sources of ignition - No Smoking.
S 24 - Avoid contact with skin.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 33 - Take precautionary measures against static discharge.
 
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:
4 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
oral-rat LD50 1850 mg/kg
LUNGS, THORAX, OR RESPIRATION: DYSPNEA BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)
Food and Cosmetics Toxicology. Vol. 2, Pg. 327, 1964.

oral-rabbit LD50 2075 mg/kg
Industrial Medicine and Surgery. Vol. 41, Pg. 31, 1972.

oral-guinea pig LD50 1110 mg/kg
BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) GASTROINTESTINAL: GASTRITIS
Food and Cosmetics Toxicology. Vol. 2, Pg. 327, 1964.

Dermal Toxicity:
skin-rabbit LD50 > 20 ml/kg
AMA Archives of Industrial Hygiene and Occupational Medicine. Vol. 10, Pg. 61, 1954.

subcutaneous-rabbit LDLo 1000 mg/kg
Food and Cosmetics Toxicology. Vol. 16, Pg. 737, 1978.

Inhalation Toxicity:
inhalation-rat LCLo 8000 ppm/4H
AMA Archives of Industrial Hygiene and Occupational Medicine. Vol. 10, Pg. 61, 1954.

 
Safety in Use Information:
Category: flavor and fragrance agents
Recommendation for ethyl formate usage levels up to:
  2.0000 % in the fragrance concentrate.
 
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
 average usual ppmaverage maximum ppm
baked goods: -98.00000
beverages(nonalcoholic): -9.40000
beverages(alcoholic): -10.00000
breakfast cereal: --
cheese: --
chewing gum: -430.00000
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -21.00000
fruit ices: -21.00000
gelatins / puddings: 0.3500011.00000
granulated sugar: --
gravies: --
hard candy: -50.00000
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: --
 
Safety References:
European Food Safety Authority (EFSA) reference(s):

Flavouring Group Evaluation 2, Revision 1 (FGE.02) : Branched- and straight-chain aliphatic saturated primary alcohols and related esters of primary alcohols and straight-chain carboxylic acids and one straight-chain aldehyde from chemical groups 1 and 2 (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

Scientific Opinion on the safety and efficacy of straight-chain primary aliphatic alcohols/aldehydes/acids, acetals and esters with esters containing saturated alcohols and acetals containing saturated aldehydes (chemical group 1) when used as flavourings for all animal species
View page or View pdf

EPI System: View
NIOSH International Chemical Safety Cards:search
NIOSH Pocket Guide:search
NLM Hazardous Substances Data Bank:Search
Env. Mutagen Info. Center:Search
NLM Developmental and Reproductive Toxicity:Search
EPA Substance Registry Services (TSCA):109-94-4
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :8025
National Institute of Allergy and Infectious Diseases:Data
WISER:UN 1190
WGK Germany:1
ethyl formate
Chemidplus:0000109944
EPA/NOAA CAMEO:hazardous materials
RTECS:109-94-4
 
References:
 ethyl formate
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:109-94-4
Pubchem (cid):8025
Pubchem (sid):134974012
Flavornet:109-94-4
Pherobase:View
 
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 Everything Added to Food in the United States (EAFUS):View
CHEBI:View
CHEMBL:View
HMDB (The Human Metabolome Database):HMDB31229
FooDB:FDB003253
YMDB (Yeast Metabolome Database):YMDB01684
Export Tariff Code:2915.13.5000
Haz-Map:View
Typical G.C.
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Formulations/Preparations:
•areginal...is mixture of methyl formate and ethyl formate. •assay: 95% minimum. •grades: technical; fcc.
 
Potential Blenders and core components note
For Odor
balsamic
cinnamyl butyrate
FL/FR
3-
phenyl propyl alcohol
FL/FR
terpinyl cinnamate
FL/FR
caramellic
diethyl malate
FL/FR
citrus
bitter
orange peel oil brazil
FL/FR
earthy
amyl octanoate
FL/FR
ethereal
acetal
FL/FR
acetaldehyde dimethyl acetal
FL/FR
iso
amyl acetoacetate
FL/FR
iso
butyl alcohol
FL/FR
cyclohexyl formate
FL/FR
decyl propionate
FL/FR
ethyl 4-pentenoate
FL/FR
1-
hexen-3-ol
FL/FR
methyl acetate
FL/FR
2-
methyl valeraldehyde
FL/FR
propyl formate
FL/FR
fatty
butyl undecylenate
FL/FR
fermented
iso
butyl decanoate
FL/FR
hexanal diethyl acetal
FL/FR
methyl decanoate
FL/FR
3-
methyl-1-pentanol
FL/FR
floral
dimethyl anthranilate
FL/FR
fruity
acetaldehyde dihexyl acetal
FL/FR
acetaldehyde diisoamyl acetal
FL/FR
amyl decanoate
FL/FR
iso
amyl nonanoate
FL/FR
iso
butyl acetoacetate
FL/FR
butyl anthranilate
FL/FR
butyl hexanoate
FL/FR
iso
butyl propionate
FL/FR
diethyl laevo-tartrate
FL/FR
diethyl sebacate
FL/FR
ethyl (E)-2-decenoate
FL/FR
ethyl 3,5,5-trimethyl hexanoate
FR
ethyl butyrate
FL/FR
ethyl heptanoate
FL/FR
farnesyl acetone
FL/FR
geranyl acetoacetate
FL/FR
grape butyrate
FL/FR
4-
heptanone
FL/FR
methyl isobutyrate
FL/FR
methyl nonanoate
FL/FR
2-
pentanone
FL/FR
propyl heptanoate
FL/FR
sorbyl butyrate
FL/FR
green
iso
amyl formate
FL/FR
benzaldehyde dimethyl acetal
FL/FR
cognac heptanone
FL/FR
green
cognac oil
FL/FR
(Z)-3-
hexen-1-yl butyrate
FL/FR
(E)-2-
hexen-1-yl valerate
FL/FR
hexyl isobutyrate
FL/FR
hexyl phenyl acetate
FL/FR
tiglaldehyde
FL/FR
herbal
iso
amyl tiglate
FL/FR
anthemis nobilis flower oil roman
FL/FR
clary sage concrete
FL/FR
white
cognac oil
FL/FR
ethyl chrysanthemate
FR
phenethyl senecioate
FL/FR
honey
methyl hydrocinnamate
FL/FR
propyl phenyl acetate
FL/FR
roasted
2-
methyl-1-butanol
FL/FR
soapy
ethyl undecanoate
FL/FR
spicy
cinnamyl isovalerate
FL/FR
waxy
allyl nonanoate
FL/FR
iso
amyl laurate
FL/FR
ethyl nonanoate
FL/FR
ethyl octanoate
FL/FR
octanol
FL/FR
phenethyl octanoate
FL/FR
winey
butyl angelate
FL/FR
2-
hexanol
FL/FR
For Flavor
No flavor group found for these
acetaldehyde 1,3-octane diol acetal
FL
acetaldehyde diisoamyl acetal
FL/FR
4-
acetyl-2-isopropenyl pyridine
FL
amyl decanoate
FL/FR
amyl octanoate
FL/FR
iso
amyl tiglate
FL/FR
2-
amyl-5 or 6-keto-1,4-dioxane
FL
butyl angelate
FL/FR
iso
butyl decanoate
FL/FR
iso
butyraldehyde propylene glycol acetal
FL
decyl propionate
FL/FR
diethyl laevo-tartrate
FL/FR
diethyl malate
FL/FR
ethyl 4-pentenoate
FL/FR
ethyl aconitate
FL
farnesyl acetone
FL/FR
geranyl acetoacetate
FL/FR
hexanal diethyl acetal
FL/FR
2-
hexanol
FL/FR
methyl hydrocinnamate
FL/FR
2-
methyl-1-butanol
FL/FR
phenethyl senecioate
FL/FR
sorbyl propionate
FL
burnt
burnt
2-
methoxypyridine
FL
citrus
cognac heptanone
FL/FR
ethereal
acetaldehyde dimethyl acetal
FL/FR
iso
butyl alcohol
FL/FR
methyl acetate
FL/FR
methyl isobutyrate
FL/FR
fatty
iso
amyl laurate
FL/FR
methyl decanoate
FL/FR
fruity
iso
amyl acetoacetate
FL/FR
iso
butyl acetoacetate
FL/FR
butyl anthranilate
FL/FR
butyl hexanoate
FL/FR
iso
butyl propionate
FL/FR
cinnamyl isovalerate
FL/FR
diethyl sebacate
FL/FR
dimethyl anthranilate
FL/FR
ethyl (E)-2-decenoate
FL/FR
ethyl butyrate
FL/FR
ethyl heptanoate
FL/FR
4-
heptanone
FL/FR
hexyl phenyl acetate
FL/FR
bitter
orange peel oil brazil
FL/FR
2-
pentanone
FL/FR
phenethyl octanoate
FL/FR
propyl formate
FL/FR
sorbyl butyrate
FL/FR
terpinyl cinnamate
FL/FR
tiglaldehyde
FL/FR
fusel
white
cognac oil
FL/FR
green
cognac oil
FL/FR
green
acetaldehyde dihexyl acetal
FL/FR
iso
amyl formate
FL/FR
benzaldehyde dimethyl acetal
FL/FR
cyclohexyl formate
FL/FR
2-
ethyl butyraldehyde
FL
grape butyrate
FL/FR
(Z)-3-
hexen-1-yl butyrate
FL/FR
(E)-2-
hexen-1-yl valerate
FL/FR
1-
hexen-3-ol
FL/FR
(E)-2-
hexenal diethyl acetal
FL
hexyl isobutyrate
FL/FR
4-
methyl-2-pentenal
FL
herbal
anthemis nobilis flower oil roman
FL/FR
clary sage concrete
FL/FR
honey
propyl phenyl acetate
FL/FR
musty
propionaldehyde
FL
nutty
acetal
FL/FR
spicy
3-
phenyl propyl alcohol
FL/FR
vegetable
2-
methyl valeraldehyde
FL/FR
waxy
allyl nonanoate
FL/FR
butyl undecylenate
FL/FR
ethyl nonanoate
FL/FR
ethyl octanoate
FL/FR
ethyl undecanoate
FL/FR
octanol
FL/FR
propyl heptanoate
FL/FR
whiskey
3-
methyl-1-pentanol
FL/FR
winey
iso
amyl nonanoate
FL/FR
cinnamyl butyrate
FL/FR
methyl nonanoate
FL/FR
 
Potential Uses:
FRalmond
FRapple
FRapricot
FLbeer
FRblackberry
FLbrandy
FRbutter
FRclary sage oil replacer
FRcoffee
FRcurrant
 ethereal
FRfruit
FRgrape
FRhoney
FRlemon
FRmalt
 melon watermelon muskmelon cantaloupe
FRmulberry
FRpeach
FRpear
FRpineapple
FRplum mirabelle plum
FRquince
FRraspberry
FRreseda
FRsaffron
FRstrawberry
FLtea
 topnotes
FL/FRvalerian
FLwhiskey
 
Occurrence (nature, food, other):note
 apple fruit
Search Trop Picture
 beer
Search PMC Picture
 brandy
Search PMC Picture
 butter
Search PMC Picture
 cabbage
Search Trop Picture
 jasmin absolute china @ trace%
Data GC Search Trop Picture
 onion
Search Trop Picture
 pineapple fruit
Search Trop Picture
 plum fruit
Search Trop Picture
 quince fruit
Search Trop Picture
 raspberry red raspberry fruit
Search Trop Picture
 rum
Search PMC Picture
 sage clary sage
Search Trop Picture
 strawberry wild strawberry fruit
Search Trop Picture
 vinegar
Search Picture
 
Synonyms:
 areginal
 carboxylic acid oxaethane
 ethyl ester of formic acid
nat.ethyl formate
 ethyl formate (natural)
 ethyl formate FCC
 ethyl formate natural
 ethyl formate naturel
 ethyl formic ester
 ethyl methanoate
 formic acid ethyl ester
 formic ether
 

Articles:

PubMed:Postharvest control of western flower thrips (Thysanoptera: Thripidae) and California red scale (Hemiptera: Diaspididae) with ethyl formate and its impact on citrus fruit quality.
PubMed:Ethyl formate plus methyl isothiocyanate--a potential liquid fumigant for stored grains.
PubMed:Effect of ionization on infrared and electronic absorption spectra of methyl and ethyl formate in the gas phase and in astrophysical H2O ice: a computational study.
PubMed:Efficacy of vaporised ethyl formate/carbon dioxide formulation against stored-grain insects: effect of fumigant concentration, exposure time and two grain temperatures.
PubMed:Field evaluation of vaporised ethyl formate and carbon dioxide for fumigation of stored wheat.
PubMed:Modelling the kinetics of ethyl formate sorption by wheat using batch experiments.
PubMed:The aromatic character of thienopyrrole-modified 20π-electron porphyrinoids.
PubMed:Identification of ethyl formate as a quality marker of the fermented off-note in coffee by a nontargeted chemometric approach.
PubMed:Fumigation of wheat using liquid ethyl formate plus methyl isothiocyanate in 50-tonne farm bins.
PubMed:Improved efficacy of ethyl formate against stored grain insects by combination with carbon dioxide in a 'dynamic' application.
PubMed:Ethyl formate - alternative dispersed solvent useful in preparing PLGA microspheres.
PubMed:Isomer-specific fuel destruction pathways in rich flames of methyl acetate and ethyl formate and consequences for the combustion chemistry of esters.
PubMed:Ethyl formate as a postharvest fumigant for selected pests of table grapes.
PubMed:The proton inventory technique in a dual mechanistic system: the spontaneous hydrolysis of ethyl formate.
PubMed:Evaluation of microwave irradiation for analysis of carbonyl sulfide, carbon disulfide, cyanogen, ethyl formate, methyl bromide, sulfuryl fluoride, propylene oxide, and phosphine in hay.
PubMed:Experimental and modeling study of the thermal decomposition of C3-C5 ethyl esters behind reflected shock waves.
PubMed:BF3·Et2O-Catalyzed Formal [3 + 2] Reaction of Aziridinofullerenes with Carbonyl Compounds.
PubMed:[Study on quality standard of Selaginella moellendorffii].
PubMed:A systematic approach for optimizing the robustness of pulse sequence elements with respect to couplings, offsets, and B1-field inhomogeneities (COB).
PubMed:Zinc catalysts for on-demand hydrogen generation and carbon dioxide functionalization.
PubMed:Novel series of 17β-pyrazolylandrosta-5,16-diene derivatives and their inhibitory effect on 17α-hydroxylase/C(17,20)-lyase.
PubMed:Molecular analysis of volatile metabolites released specifically by Staphylococcus aureus and Pseudomonas aeruginosa.
PubMed:Different families of volatile organic compounds pollution control by microporous carbons in temperature swing adsorption processes.
PubMed:Crucial aspects of high performance thin layer chromatography quantitative validation. The case of determination of rosmarinic acid in different matrices.
PubMed:Reactions of the terminal Ni(II)-OH group in substitution and electrophilic reactions with carbon dioxide and other substrates: structural definition of binding modes in an intramolecular Ni(II)...Fe(II) bridged site.
PubMed:Synthesis and electrophilic substitutions of novel pyrazolo[1,5-c]-1,2,4-triazolo[4,3-a]pyrimidines.
PubMed:Chirped pulse Fourier transform microwave study of 2,2,2-trifluoroethyl formate.
PubMed:A remarkable multicomponent cascade sequence for the formation of a spirocyclic polyether.
PubMed:Another paradigm in solvent extraction-based microencapsulation technologies.
PubMed:1,3-Dihy-droxy-2-(hy-droxy-meth-yl)propan-2-aminium formate.
PubMed:Strigolactone analogs derived from ketones using a working model for germination stimulants as a blueprint.
PubMed:Fuel-specific influences on the composition of reaction intermediates in premixed flames of three C5H10O2 ester isomers.
PubMed:Selective determination of aloin in different matrices by HPTLC densitometry in fluorescence mode.
PubMed:Selected ion flow tube-mass spectrometry for absolute quantification of aroma compounds in the headspace of dry fermented sausages.
PubMed:Determination of polyphenolics in extracts of Potentilla species by high-performance thin-layer chromatography photodensitometry method.
PubMed:The atmospheric oxidation of diethyl ether: chemistry of the C2H5-O-CH(O.)CH3 radical between 218 and 335 K.
PubMed:Toxicities of 31 volatile low molecular weight compounds against Aedes aegypti and Culex quinquefasciatus.
PubMed:Modeling the heat and mass transfers in temperature-swing adsorption of volatile organic compounds onto activated carbons.
PubMed:Analysis of formic acid in air samples.
PubMed:Reverse micelle-based microencapsulation of oxytetracycline hydrochloride into poly-d,l-lactide-co-glycolide microspheres.
PubMed:Gas-phase fragmentation study of novel synthetic 1,5-benzodiazepine derivatives using electrospray ionization tandem mass spectrometry.
PubMed:Evidence for C-H...O=C bonding in coadsorbed aromatic-carbonyl systems on Pt(111).
PubMed:Simultaneous determination of formic acid and formaldehyde in pharmaceutical excipients using headspace GC/MS.
PubMed:Solvent effects on the structural and formyl substrate reactivity properties of a nitrogen/sulfur-ligated zinc hydroxide complex.
PubMed:Cytochrome c oxidase inhibition in the rice weevil Sitophilus oryzae (L.) by formate, the toxic metabolite of volatile alkyl formates.
PubMed:In vitro efficacy of plant volatiles for inhibiting the growth of fruit and vegetable decay microorganisms.
PubMed:Synthesis of modified nucleosides for incorporation of formyletheno and carboxyetheno adducts of adenine nucleosides into oligonucleotides.
PubMed:Degradation patterns of tetracycline antibiotics in reverse micelles and water.
PubMed:Evaluation of volatile low molecular weight insecticides using Drosophila melanogaster as a model.
PubMed:Characteristics of felodipine-located poly(epsilon-caprolactone) microspheres.
PubMed:Surfactant-free microspheres of poly(epsilon-caprolactone)/poly (ethylene glycol)/poly(epsilon-caprolactone) triblock copolymers as a protein carrier.
PubMed:Oxidative pyrolysis of organic ion exchange resins in the presence of metal oxide catalysts.
PubMed:Determination of N-nitrosodiethanolamine in urine by gas chromatography thermal energy analysis: application in workers exposed to aqueous metalworking fluids.
PubMed:Determination of alpha-bisabolol and d-panthenol in cosmetic products by gas chromatography.
PubMed:Access to fluorescent probes via allyl glycosides: the synthesis of a Brucella trisaccharide epitope linked to a coumarin.
PubMed:Synthesis of certain 2-aminoadamantane derivatives as potential antimicrobial agents.
PubMed:Acetone, methyl ethyl ketone, ethyl acetate, acetonitrile and other polar aprotic solvents are strong inducers of aneuploidy in Saccharomyces cerevisiae.
PubMed:Absorption dynamics of organic chemical transport across trout gills as related to octanol-water partition coefficient.
PubMed:[Quality standard for Xindi soft capsule].
PubMed:From chemosensory thresholds to whole body exposures-experimental approaches evaluating chemosensory effects of chemicals.
PubMed:Development of new reverse micellar microencapsulation technique to load water-soluble drug into PLGA microspheres.
PubMed:Flexible synthesis of enantiomerically pure 2,8-dialkyl-1,7-dioxaspiro[5.5]undecanes and 2,7-dialkyl-1,6-dioxaspiro[4.5]decanes from propargylic and homopropargylic alcohols.
PubMed:Ortho-Directed Lithiation of omega-Phenoxy Alcohols.
PubMed:Cooperative reactivity of early-late heterodinuclear transition metal complexes with polar organic substrates
PubMed:The synthesis of antibody binding-site probes: a hexasaccharide and two pentasaccharides related to the Brucella A antigen and prepared by in situ activation of thioglycosides with bromine.
PubMed:The design and synthesis of antibody binding site probes: three pentasaccharide analogues of the Brucella A antigen prepared by activation in situ of thioglycosides with bromine.
PubMed:1,2-Dihydro-2-oxo-6-(2,2-dimethylpropyl)-3-pyridinecarboxylic acid, analogues, and derivatives. A new class of oral hypoglycemic agents.
PubMed:Synthesis and pharmacological activity of derivatives of exo-trimethylenenorbornane. II.
PubMed:[Steroidal heterocyclic compounds: [16,15-c]-pyrazole derivatives of estradiol and of estrone].
PubMed:Characterization of esterases produced by a ruminal bacterium identified as Butyrivibrio fibrisolvens.
PubMed:Partial biochemical characterization of the activated esterase required in the complement-dependent chemotaxis of rabbit polymorphonuclear leukocytes.
 
Notes:
Fruit lifter. Found in various foods, e.g. cooked apple, orange juice, pineapple, other fruits, raw cabbage, coffee, black tea, wheat bread, white clover, sorghum. Used as a flavouring agent
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