methyl furoate

General Material Information

Preferred name	methyl furoate
Trivial Name	Furancarboxylic acid, methyl ester
Short Description	3-furancarboxylic acid, methyl ester
Formula	C6 H6 O3
CAS Number	1334-76-5
ECHA Number	215-614-6
FDA UNII	WS10TS94NA
Nikkaji Number	J127.896G
MDL	MFCD06203671
Bio Activity Summary	External link
NMR Predictor	External link
Synonyms	furan carboxylic acid methyl ester furancarboxylic acid methyl ester 3-furancarboxylic acid methyl ester 3-furancarboxylic acid, methyl ester 3-furancarboxylicacidmethylester furoic acid methyl ester furoic acid, methyl ester 3-furoic acid, methyl ester methyl 3-furancarboxylate methyl 3-furoate methyl furan carboxylate methyl furan-3-carboxylate Furancarboxylic acid, methyl ester Methyl furancarboxylate

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Literature & References

	methyl furan-3-carboxylate
NIST Chemistry WebBook:	Search Inchi
Pubchem (cid):	14918
Pubchem (sid):	134979316
Pherobase:	View

Publications by PubMed
Mometasone furoate-loaded cold processed oil-in-water emulsions: in vitro and in vivo studies.
Asymmetric synthesis of both enantiomers of arteludovicinolide A.
An efficient method for the determination of furan derivatives in apple cider and wine by solid phase extraction and high performance liquid chromatography--diode array detector.
1H NMR spectra. Part 29§: Proton chemical shifts and couplings in esters--the conformational analysis of methyl γ-butyrolactones.
Efficacy and safety of 15(R/S)-methyl-lipoxin A(4) in topical treatment of infantile eczema.
Chemical and biochemical study of industrially produced San Simón da Costa smoked semi-hard cow's milk cheeses: Effects of storage under vacuum and different modified atmospheres.
Gateways to clinical trials.
Gateways to clinical trials.
Characterization of ZK 245186, a novel, selective glucocorticoid receptor agonist for the topical treatment of inflammatory skin diseases.
Enantioselective synthesis of furo[2,3-b]furans, a spongiane diterpenoid substructure.
Pentane-1,5-diol as a percutaneous absorption enhancer.
Stability indicating reversed-phase liquid chromatographic determination of metronidazole benzoate and diloxanide furoate as bulk drug and in suspension dosage form.
A ceramic electrochemical microreactor for the methoxylation of methyl-2-furoate with direct mass spectrometry coupling.
Enzymatic hydrolysis of diloxanide furoate in the presence of beta-cyclodextrin and its methylated derivatives.
Mometasone furoate degradation and metabolism in human biological fluids and tissues.
Biomimetic cycloaddition approach to tropolone natural products via a tropolone ortho-quinone methide.
Generation of Maillard compounds from inulin during the thermal processing of Agave tequilana Weber Var. azul.
Phenolic compounds from tournefortia sarmentosa
The therapeutic efficacy of mometasone furoate cream 0.1% applied once daily vs clobetasol propionate cream 0.05% applied twice daily in chronic eczema.
Topical mometasone. A review of its pharmacological properties and therapeutic use in the treatment of dermatological disorders.
Metabolic reduction of novel 3,4-dichloro-5-nitrofurans in Salmonella typhimurium.
Mutagenicity of N- and O-acetyl derivatives of methyl 3,4-diphenyl-5-hydroxylamino-2-furoate and N-hydroxy-4-aminobiphenyl in Salmonella typhimurium.
Cytokine inhibition by a novel steroid, mometasone furoate.
Platelet activating factor antagonist design. 3. X-ray crystal structure and intermolecular crystal lattice interactions of methyl trans-4-acetoxymethyl-4,5-dihydro-2,5-bis(3,4-methylenedioxyphenyl)- 3-furancarboxylate.
Platelet activating factor antagonist design: structure of methyl trans-5-(3,4-dimethoxyphenyl)-2,3,4,5-tetrahydro-2-oxo-4- furancarboxylate.
17-Heteroaroyl esters of corticosteroids. 2. 11 beta-Hydroxy series.
Synthesis and structure-activity studies of corticosteroid 17-heterocyclic aromatic esters. 1. 9 alpha, 11 beta-dichloro series.
Mutagenicity of 3,4-diphenyl-5-nitrofuran analogs in Salmonella typhimurium.
Formation of novel nitrofuran metabolites in xanthine oxidase-catalyzed reduction of methyl 5-nitro-2-furoate.
Reduction of methyl 5-nitro-2-furoate by xanthine oxidase: an evidence for hydroxylaminofuran formation.
Synthesis and local anesthetic activity of benzo[b]furan derivatives.

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
Typical G.C.
VCF-Online:	VCF Volatile Compounds in Food
ChemSpider:	View
EFSA Update of results on the monitoring of furan levels in food:	Read Report
EFSA Previous report: Results on the monitoring of furan levels in food:	Read Report
EFSA Report of the CONTAM Panel on provisional findings on furan in food:	Read Report

Suppliers

BOC Sciences	M&U International
R C Treatt & Co Ltd	M&U International LLC
R C Treatt and Co Ltd

PhysChem Properties

Material listed in food chemical codex	No
Molecular weight	126.11141967773
Boiling Point	154 to 155°C @ 760 mm Hg
Vapor Pressure	2.436 mmHg @ 25 °C
Flash Point TCC Value	47.3 °C TCC
logP (o/w)	1.297 est
Solubility
alcohol	Yes
water, 1.332e+004 mg/L @ 25 °C (est)	Yes

Organoleptic Properties

Odor Type: Berry
berry, fruity, winey
General comment	At 100.00 %. berry fruity winey

Occurrences

Potential Uses

Applications	natural substances and extractives
Odor purposes	Fungus

Safety Information

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.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined

Safety in use information

Category:
natural substances and extractives
Recommendation for methyl furoate usage levels up to:
	not for fragrance use.

Recommendation for methyl furoate flavor usage levels up to:
	not for flavor use.

Safety references

EPI System: View

AIDS Citations:Search

Cancer Citations:Search

Toxicology Citations:Search

EPA Substance Registry Services (TSCA):1334-76-5

EPA ACToR:Toxicology Data

EPA Substance Registry Services (SRS):Registry

Laboratory Chemical Safety Summary :14918

National Institute of Allergy and Infectious Diseases:Data

methyl furan-3-carboxylate

Chemidplus:0001334765