Grundinformationen
- Standard-SMILES
CC(=O)OCCc1scnc1C- InChIKey
CRTCWNPLKVVXIX-UHFFFAOYSA-N- Summenformel
- C8H11NO2S
- Durchschnittliche Molmasse
- 185,25 g/mol
- Monoisotopische Masse
- 185,05104959
Überblick
5-(2-Hydroxyethyl)-4-methylthiazole acetate is a member of thiazoles.
Namen und Bezeichner
- Bevorzugter Name
- 4-Methyl-5-thiazoleethanol acetate
- IUPAC
- 2-(4-methyl-1,3-thiazol-5-yl)ethyl acetate
- Lokaler Name
- 2-(4-Methylthiazol-5-yl)ethylacetat
- Englischer Name
- 4-Methyl-5-thiazolylethyl acetate
- Summenformel
- C8H11NO2S
- Molmasse
- 185.24
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
656-53-1- PubChem CID
- 61192
- DTXSID
DTXSID8060959- ChEBI
CHEBI:179422- UNII
- 885387Q99B
- EC Number
- 211-515-7
- Nikkaji
- J24.663H
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 1,4
- Polarare Oberfläche (TPSA)
- 67,4 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 4
- Frei drehbare Bindungen
- 4
- Schwere Atome
- 12
- Formalladung
- 0
- Komplexität
- 163
Experimentelle und physikochemische Eigenschaften
Solubility
Slightly soluble in water; Soluble in organic solvents
Miscible at room temperature (in ethanol)
Boiling Point
117.00 to 118.00 °C. @ 6.00 mm Hg
117-118 °C (6 mm Hg)
Physical Description
Solid
Colourless to yellow liquid; meaty odour
Physikochemische Eigenschaften
- Schmelzpunkt
- 112 °C · 112 °C
- Siedepunkt
- 117 · 117-118 °C6 mm Hg(lit.)
- Dichte
- 1.147 g/mL · 1.147 g/mL at 25 °C(lit.)
- Brechungsindex
- 20 · n20/D 1.51(lit.)
- FEMA
- 3205 · 3205 | 4-METHYL-5-THIAZOLEETHANOL ACETATE
- Flammpunkt
- 230 °F · >230 °F
- storage temp.
- 2 · 2-8°C
- pka
- 3.26 · 3.26±0.10(Predicted)
- Aggregatzustand
- Liquid
- Wichte
- 1.147 · 1.147
- Farbe
- Clear brown
- Geruch (Odor)
- 100 % · at 100.00 %. meaty beef juice beef gravey
- Geruchsart
- meaty
- Biologische Quelle
- synthetic
- JECFA Number
- 1054 · 1054
- Major Application
- flavors and fragrances
- InChI
- 1S/C8H11NO2S/c1-6-8(12-5-9-6)3-4-11-7(2)10/h5H,3-4H2,1-2H3
- InChIKey
- CRTCWNPLKVVXIX-UHFFFAOYSA-N
- SMILES
- CC(=O)OCCc1scnc1C
- LogP
- 0.98 · 0.98
- CAS Datenbank
- 656 · 656-53-1(CAS DataBase Reference)
- EPA chemische Informationen
- 5 · 5-Thiazoleethanol, 4-methyl-, acetate (ester) (656-53-1)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
This chemical does not meet GHS hazard criteria for 6.3% (90 of 1424) of reports.
Warning
H332 (90.4%): Harmful if inhaled [Warning Acute toxicity, inhalation]
P261, P271, P304+P340, and P317 (click each P-code to see the statement)
Aggregated GHS information provided per 1424 reports by companies from 11 notifications to the ECHA C&L Inventory.
Gefahrenhinweise
Regulatory Information
Chemical: 5-Thiazoleethanol, 4-methyl-, acetate (ester)
Commission Regulation (EC) No 1565/2000 (Repealed by Com. Implementing Reg. (EU) No 872/2012)
5-Thiazoleethanol, 4-methyl-, acetate (ester): Does not have an individual approval but may be used under an appropriate group standard
Sicherheitsdaten
- wgk
- 3
- tsca
- TSCA listed
- ridadr
- UN 3334
- hs_code
- 29341000
- risk_code
- 36/37/38
- hazard_code
- Xi
- safety_code
- 26-37/39-24/25
- Speicherklasse
- 10 - Combustible liquids
- Hazard Classifications
- Acute Tox. 4 InhalationAcute Tox. 4 OralSTOT SE 3
Chemie und Industrie
Pharmakologische Informationen
Verwendung und Herstellung
Use Classification
Fragrance Ingredients
Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes
Flavoring Agents -> JECFA Flavorings Index
Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes
Anwendungen
BeschreibungMay be prepared from 2-methylthio-4-methyl-5-(2-acetoxyethyl)- thiazole and AlHg; by dehydrogenation with sulfur at 130°C of the (i-acetyl derivative of 4-methyl-5-(P-hydroxyethyl)-3-thiazoline.
Verwenden4-Methyl-5-thiazolylethyl Acetate is used in biological study for research on contribution of oxidized tallow to aroma characteristics of beeflike process flavor assessed by gas chromatography-mass spectrometry and partial least squares regression.
Darstellung
synthetischeFrom 2-methylthio-4-methyl-5-(2-acetohxyethyl)-thiazole and AlHg; by dehydrogenation with sulfur at 130°C of the β-acetyl derivative of 4-methyl-5-(β-hydroxyethyl)-3-thiazoline
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