Grundinformationen
- Standard-SMILES
O=C(O)[C@H](O)[C@@H](O)C(=O)O- InChIKey
FEWJPZIEWOKRBE-JCYAYHJZSA-N- Summenformel
- C4H6O6
- Durchschnittliche Molmasse
- 150,09 g/mol
- Monoisotopische Masse
- 150,01643791
Namen und Bezeichner
- Bevorzugter Name
- L-Tartaric acid
- IUPAC
- (2R,3R)-2,3-dihydroxybutanedioic acid
- Lokaler Name
- (+-)-Weinsure
- Englischer Name
- DL-Tartaric acid
- Summenformel
- C4H6O6
- Molmasse
- 150.09
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
133-37-9、868-14-4、87-69-4- PubChem CID
- 444305
- DTXSID
DTXSID8023632- ChEMBL
CHEMBL1236315- ChEBI
CHEBI:15671- UNII
- 4J4Z8788N8、W4888I119H
- EC Number
- 201-766-0、205-105-7
- Nikkaji
- J31.839F
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- -1,9
- Polarare Oberfläche (TPSA)
- 115 Ų
- H-Brücken-Donoren
- 4
- H-Brücken-Akzeptoren
- 6
- Frei drehbare Bindungen
- 3
- Schwere Atome
- 10
- Formalladung
- 0
- Komplexität
- 134
Physikochemische Eigenschaften
- Schmelzpunkt
- 210 · 210-212 °C(lit.)
- Siedepunkt
- 191.59 °C · 191.59°C (rough estimate)
- Dichte
- 1.788 · 1.788
- Dampfdruck
- 0.1 hPa · <0.1 hPa (20 °C)
- FEMA
- 3044 · 3044 | TARTARIC ACID (D-, L-, DL-, MESO-)
- Brechungsindex
- 1.586 · 1.5860 (estimate)
- Flammpunkt
- 210 °C · 210 °C
- storage temp.
- 30 °C · Store below +30°C.
- Löslichkeit
- 2 O: · H2O: 0.1 g/mL, clear
- Aggregatzustand
- Liquid
- pka
- 3.03 · 3.03, 4.37(at 25℃)
- Farbe
- White
- PH
- 3.19 · 3.19(1 mM solution);2.58(10 mM solution);2.03(100 mM solution);
- Geruch (Odor)
- 100 % · at 100.00 %. very mild caramellic
- Geruchsart
- odorless
- Biologische Quelle
- synthetic
- Wasserlöslichkeit
- soluble
- Merck
- 14 · 14,9069
- JECFA Number
- 621 · 621
- BRN
- 1725148 · 1725148
- Dielectric constant
- 35.9 · 35.9(-10℃)
- Stabilität
- Stable. Incompatible with bases, oxidizing agents, reducing agents, silver.
- Major Application
- flavors and fragrances
- Kosmetik-Inhaltsstoffe Funktionen
- BUFFERINGFRAGRANCE
- InChI
- 1S/C4H6O6/c5-1(3(7)8)2(6)4(9)10/h1-2,5-6H,(H,7,8)(H,9,10)/t1-,2-/m0/s1
- InChIKey
- FEWJPZIEWOKRBE-UHFFFAOYSA-N
- SMILES
- O[C@@H]([C@H](O)C(O)=O)C(O)=O
- LogP
- -1.43 · -1.43
- CAS Datenbank
- 133 · 133-37-9(CAS DataBase Reference)
- NIST chemische Informationen
- Tartaric acid(133-37-9)
- EPA chemische Informationen
- 2 · Butanedioic acid, 2,3-dihydroxy-, (2R,3R)-rel- (133-37-9)
Sicherheit und Regulatorisches
Sicherheitsdaten
- wgk
- 3
- tsca
- TSCA listed
- hs_code
- 29181200
- risk_code
- 36/37/38-41
- hazard_code
- Xi
- safety_code
- 26-37/39-36
- Speicherklasse
- 11 - Combustible Solids
- Hazard Classifications
- Eye Dam. 1
- Selbstentzündungstemperatur
- 425 °C
Chemie und Industrie
Anwendungen
Occurrenced-Tartaric acid occurs in many fruits or other parts of the plant, free or combined with potassium, calcium or magnesium. It is also reported found in raw, lean fish, white wine, red wine and port wine.
VerwendenDL-Tartaric acid is used as a synergist for antioxidants, emulsifier, sequestrant and flavoring agent. It is also added with citric acid to prepare effervescent salts, thereby enhancing the taste of oral medications. It is also utilized in pigments, processing aids, ink, toner and colorant products. It acts as a chelating agent in metal and farming industries. Further, it is used as lubricant and grease. It is mixed with sodium bicarbonate and used as a leavening agent in food preparation. In the pharmaceutical industry, it is utilized in the preparation of tartar emetic, which is used in cough syrup as an expectorant.
Darstellung
synthetischeThe tartrates used in commerce are obtained as a by-product of wine manufacture and have the L(+) configuration. Produced from argols or wine lees, which are formed in the manufacture of wine by extracting the potassium acid tartrate, transforming this into the calcium salt and then acidifying with dilute sulfuric acid; also by oxidation of d-glucose with nitric acid. The dl-tartaric acid is obtained by boiling the d-tartaric acid with an aqueous solution of NaOH or by oxidation of fumaric acid. The l- and the meso-tartaric acid are also known, but are less important.
Vor- und nachgelagerte Produkte
Vorgelagerte Rohstoffe
Nachgelagerte Produkte
Anbieter50 Anbieter
Ergänzende Hinweise
DefinitionChEBI: DL-Tartaric acid is a tetraric acid that is butanedioic acid substituted by hydroxy groups at positions 2 and 3. It has a role as a human xenobiotic metabolite and a plant metabolite. It is a conjugate acid of a 3-carboxy-2,3-dihydroxypropanoate.
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