(+-)-Weinsure

Bezeichnung:(+-)-Weinsure

CAS-Nr133-37-9

Englisch Name:DL-Tartaric acid

CBNumberCB5212873

SummenformelC4H6O6

Molgewicht150.09

MOL-Datei133-37-9.mol

Synonyma

(+-)-Weinsure

Racemische Weins?ure

DL-Weins?ure

(+-)-Weinsure physikalisch-chemischer Eigenschaften

Schmelzpunkt	210-212 °C(lit.)
Siedepunkt	191.59°C (rough estimate)
alpha	[α]D20 -0.2～+0.2° (c=20, H2O)
Dichte	1.788
Dampfdruck	<0.1 hPa (20 °C)
Brechungsindex	1.5860 (estimate)
FEMA	3044 \| TARTARIC ACID (D-, L-, DL-, MESO-)
Flammpunkt	210 °C
storage temp.	Store below +30°C.
Löslichkeit	H₂O: 0.1 g/mL, clear
Aggregatzustand	Liquid
pka	3.03, 4.37(at 25℃)
Farbe	White
PH	3.19(1 mM solution);2.58(10 mM solution);2.03(100 mM solution);
Geruch (Odor)	at 100.00 %. very mild caramellic
Geruchsart	odorless
Wasserlöslichkeit	soluble
Merck	14,9069
JECFA Number	621
BRN	1725148
Dielectric constant	35.9（-10℃）
Stabilität	Stable. Incompatible with bases, oxidizing agents, reducing agents, silver.
InChIKey	FEWJPZIEWOKRBE-UHFFFAOYSA-N
LogP	-1.43
CAS Datenbank	133-37-9(CAS DataBase Reference)
NIST chemische Informationen	Tartaric acid(133-37-9)
EPA chemische Informationen	Butanedioic acid, 2,3-dihydroxy-, (2R,3R)-rel- (133-37-9)

Sicherheit

Kennzeichnung gefährlicher	Xi
R-Sätze:	36/37/38-41
S-Sätze:	26-37/39-36
WGK Germany	3
Selbstentzündungstemperatur	425 °C
TSCA	Yes
HS Code	29181200

Gefahreninformationscode (GHS)

DL-Tartaric acid Chemische Eigenschaften,Einsatz,Produktion Methoden

ERSCHEINUNGSBILD
WEISSES KRISTALLINES PULVER.
CHEMISCHE GEFAHREN
Mittelstarke Säure in wässriger Lösung.
ARBEITSPLATZGRENZWERTE
TLV nicht festgelegt (ACGIH 2005).
MAK nicht festgelegt (DFG 2005).
AUFNAHMEWEGE
Aufnahme in den Körper durch Inhalation oder durch Verschlucken.
INHALATIONSGEFAHREN
Verdampfung bei 20°C vernachlässigbar; eine gesundheitsschädliche Partikelkonzentration in der Luft kann jedoch beim Dispergieren schnell erreicht werden.
WIRKUNGEN BEI KURZZEITEXPOSITION
WIRKUNGEN BEI KURZZEITEXPOSITION:
ätzend. Die Substanz verätzt die Augen, die Haut und die Atemwege. ätzend beim Verschlucken. Inhalation des Aerosols kann zu Lungenödem führen (s.Anm.). Die Auswirkungen treten u.U. verzögert ein. ärztliche Beobachtung notwendig.
LECKAGE
Verschüttetes Material in Behältern sammeln; falls erforderlich durch Anfeuchten Staubentwicklung verhindern. Persönliche Schutzausrüstung: Atemschutzgerät, P2-Filter für schädliche Partikel.
R-Sätze Betriebsanweisung:
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
S-Sätze Betriebsanweisung:
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S37/39:Bei der Arbeit geeignete Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
Chemische Eigenschaften
DL-Tartaric acid is a water- and alcohol-soluble colorless crystalline solid with a characteristic acid taste and a melting temperature of 170°C(338°F). Naturally occurring tartaric acid is generally of the L-configuration (based on the absolute configuration of D-glyceric acid). The L-forms of tartrates are dextrorotatory in solution and thus are designated as L(+)-tartrates. It is also known as dihydroxy succinic acid. Tartaric acid is used as a chemical intermediate and a sequestrant,as well as in tanning, effervescent beverages, baking powder, ceramics, photography, textile processing,mirror silvering,and metal coloring.
Occurrence
d-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.
Application
DL-Tartaric acid can be used:
In the Debus–Radziszewski reaction as a weak acid for the synthesis of imidazolium ionic liquid.
As an additive in electrochemical deposition technique for the synthesis of bismuth thin films to be used as X-ray absorbers.
As a complexing agent for the synthesis of nano-crystalline indium tin oxide (ITO) powder.
As a dopant for the synthesis of polyaniline nanofibers and nanotubes by oxidation polymerization.
Verwenden
DL-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.
Definition
ChEBI: 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.
synthetische
The 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.

DL-Tartaric acid Upstream-Materialien And Downstream Produkte

(+-)-Weinsure Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

133-37-9, DL-Tartaric acid Verwandte Suche:

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