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

3-thiophene carboxaldehyde
3-formylthiophene

Supplier Sponsors

CAS Number: 498-62-4Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:207-865-5
FDA UNII: Search
Nikkaji Web:J149.677H
Beilstein Number:1932694
MDL:MFCD00005466
XlogP3:1.00 (est)
Molecular Weight:112.15108000
Formula:C5 H4 O S
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:natural substances and extractives
 
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
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Appearance:colorless to pale yellow clear liquid (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Specific Gravity:1.23000 to 1.23500 @ 20.00 °C.
Pounds per Gallon - (est).: 10.247 to 10.288
Refractive Index:1.58200 to 1.58600 @ 20.00 °C.
Boiling Point: 194.00 to 196.00 °C. @ 760.00 mm Hg
Boiling Point: 190.00 to 191.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure:0.537000 mmHg @ 25.00 °C. (est)
Flash Point: 165.00 °F. TCC ( 73.90 °C. )
logP (o/w): 1.010
Soluble in:
 water, 1.468e+004 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
3-Thiophenecarboxaldehyde >98.0%(GC)
Matrix Scientific
For experimental / research use only.
Thiophene-3-carboxaldehyde, 98%
sds
Santa Cruz Biotechnology
For experimental / research use only.
3-Thiophenecarboxaldehyde
Sigma-Aldrich: Aldrich
For experimental / research use only.
3-Thiophenecarboxaldehyde 98%
sds
TCI AMERICA
For experimental / research use only.
3-Thiophenecarboxaldehyde >98.0%(GC)
sds
 
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:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
natural substances and extractives
Recommendation for 3-thiophene carboxaldehyde usage levels up to:
 not for fragrance use.
 
Recommendation for 3-thiophene carboxaldehyde 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):498-62-4
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :68135
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
thiophene-3-carbaldehyde
Chemidplus:0000498624
 
References:
 thiophene-3-carbaldehyde
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):68135
Pubchem (sid):135024333
 
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
CHEBI:View
CHEMBL:View
HMDB (The Human Metabolome Database):Search
Export Tariff Code:2934.99.4400
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 cognac
Search PMC Picture
 
Synonyms:
3-formyl thiophene
3-formylthiophene
3-thenaldehyde
3-thienophenecarboxyaldehyde
3-thiophenaldehyde
 thiophene-3-carbaldehyde
 thiophene-3-carboxaldehyde
3-thiophenealdehyde
3-thiophenecarbaldehyde
3-thiophenecarboxaldehyde
 

Articles:

PubMed:Characterization of volatile components and odor-active compounds in the oil of edible mushroom Boletopsis leucomelas.
PubMed:The development of a one pot, regiocontrolled, three-component reaction for the synthesis of thieno[2,3-c]pyrroles.
PubMed:A biotinylated undecylthiophene copolymer bioconjugate for surface immobilization: creating an alkaline phosphatase chemiluminescence-based biosensor.
PubMed:Synthesis and carbonic anhydrase inhibitory activity of 4-substituted 2-thiophenesulfonamides.
PubMed:Synthesis and structure-activity relationships among glycosidic derivatives of 4'-demethylepipodophyllotoxin and epipodophyllotoxin, showing VM26- and VP16-213-like activities.
 
Notes:
None found
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