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(+-)-Weinsure

2,3-Dihydroxybutanedioic Acid

HCID 875
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Grundinformationen

CAS
133-37-9
Standard-SMILES
O=C(O)C(O)C(O)C(=O)O
InChIKey
FEWJPZIEWOKRBE-UHFFFAOYSA-N
Summenformel
C4H6O6
Durchschnittliche Molmasse
150,09 g/mol
Monoisotopische Masse
150,01643791

Überblick

2,3-dihydroxybutanedioic acid is a tetraric acid that is butanedioic acid substituted by hydroxy groups at positions 2 and 3. It has a role as a plant metabolite and a human xenobiotic metabolite. It is a conjugate acid of a 3-carboxy-2,3-dihydroxypropanoate.

Namen und Bezeichner

Bevorzugter Name
2,3-Dihydroxybutanedioic Acid
IUPAC
2,3-dihydroxybutanedioic acid
Lokaler Name
(+-)-Weinsure
Englischer Name
DL-Tartaric acid
Summenformel
C4H6O6
Molmasse
150.09

Namen und Synonyme

2,3-Dihydroxybutanedioic acid526-83-0GlyTouCan:G35198MQDTXCID3026986CHEBI:15674DTXSID501031477RefChem:935304G35198MQ610-885-0DL-Tartaric acid133-37-9Racemic acid
Weitere Namen anzeigen
TARTARIC ACIDdl-Tartaric acid anhydrousDL-TartaricClopidogrel Impurity 45DL-Tartaric acid concentrateButanedioic acid, 2,3-dihydroxy-, (2R,3R)-rel-DL-Tartaric acid 133-37-9 pure 99% food additives Paratartaric acid kf-wang(at)kf-chem.com
Uvic acidTraubensaureRacemic tartaric acidParatartaric acidParatartaric aicdDL-TartrateBUTANEDIOIC ACID, 2,3-DIHYDROXY-MFCD00064206

Datenbank-Bezeichner

CAS
133-37-9、526-83-0、87-69-4
PubChem CID
875
DTXSID
DTXSID501031477

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

Experimentelle und physikochemische Eigenschaften

Chemical ClassesOther Classes -> Organic Acids
DrugsPharmaceuticals
FragrancesFragrance Ingredient (Tartaric acid (d-, l-, dl-, meso-)) -> IFRA transparency List
Solubility · 2 Einträge

soluble in water and alcohol; 1 gm in 0.8 ml water

1 g in 3 ml 95% alcohol (in ethanol)

Physical Description · 2 Einträge

White solid; [ICSC] Colorless or white odorless solid; [JECFA] White odorless crystalline powder; [Acros Organics MSDS]

colourless or translucent crystals, or a white, fine to granular crystaline powder which is odourless with an acid taste

Collision Cross Section · 2 Einträge

115.46 Ų [M-H]- [CCS Type: DT; Method: single field calibrated with Agilent tune mix (Agilent)]

124.4 Ų [M+H]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]

Physikochemische Eigenschaften

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

GHS-Klassifizierung

GHS Classification · 6 Einträge

This chemical does not meet GHS hazard criteria for 5.1% (26 of 506) of reports.

Danger

H315 (22.1%): Causes skin irritation [Warning Skin corrosion/irritation]

P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P305+P354+P338, P317, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 506 reports by companies from 13 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Warning

Gefahrenhinweise

Regulatory Information · 2 Einträge

Chemical: Butanedioic acid, 2,3-dihydroxy-, (R*,R*)-(.+-.)-

REACH registered substance: (±)-tartaric acid (EC: 205-105-7)

Other Safety InformationIMAP assessments - Butanedioic acid, 2,3-dihydroxy-, (R*,R*)-(.+-.)-: Human health tier I assessment
Hazards SummaryCauses burns; Inhalation of aerosol may cause pulmonary edema; [ICSC] An irritant; [Acros Organics MSDS]
Hazard Classes and Categories · 2 Einträge

Skin Irrit. 2 (22.1%)

Skin Irrit. 2 (100%)

Toxikologische Informationen

Adverse EffectsDermatotoxin - Skin burns.
Carcinogen ClassificationNo indication of carcinogenicity to humans (not listed by IARC).

Chemie und Industrie

Verwendung und Herstellung

UsesUsed as a synergist for antioxidants, acid, emulsifier, sequestrant, and flavoring agent; [JECFA]
Household ProductsInformation on 7 consumer products that contain Tartaric acid in the following categories is provided:
Use Classification · 4 Einträge

Fragrance Ingredients

Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes

Flavouring Agent -> FLAVOURING_AGENTFood Additives -> ACID; ANTIOXIDANT_SYNERGIST; EMULSIFIER; SEQUESTRANT; SYNERGIST -> JECFA Functional Classes

Flavoring Agents -> JECFA Flavorings Index

Anwendungen · 2 Einträge

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 · 1 Eintrag

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.

Zugehörige Reaktionen

439
Reaktionsaufzeichnung erstellen
Reaktionsgleichung von HRID 1663
HRID 1663als Eduktuspto-grants-1998_03
Reaktionsgleichung von HRID 2371
HRID 2371als Eduktuspto-grants-1998_03
Reaktionsgleichung von HRID 2525
HRID 2525als Eduktuspto-grants-1998_03
Reaktionsgleichung von HRID 3989
HRID 3989als Eduktuspto-grants-1988_02
Reaktionsgleichung von HRID 6511
HRID 6511als Eduktuspto-grants-1993_09
Reaktionsgleichung von HRID 15607
HRID 15607als Eduktuspto-grants-2010_06
Reaktionsgleichung von HRID 26584
HRID 26584als Produktuspto-grants-1979_04
Reaktionsgleichung von HRID 35217
HRID 35217als Eduktuspto-grants-1988_08
Seite 1 von 55

Notizen zur Verbindung

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Auf dieser SeiteGrundinformationenÜberblickNamen und BezeichnerEigenschaftenSicherheit und RegulatorischesChemie und IndustrieZugehörige ReaktionenNotizen zur Verbindung
Weitere Aktionen
Neue NotizNeue ReaktionAnfrage stellen
ChEMBL
CHEMBL333714
ChEBI
CHEBI:15674
EC Number
205-105-7、610-885-0
Nikkaji
J56.048K
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)

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

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

CalciumtartratDihydrogenwolframatMaleinsäureMaleinsäureanhydridWasserstoffperoxidSodium pyruvate(+/-)-trans-Epoxysuccinic acidD(-)-Tartaric acidcis-EpoxybernsteinsurePenta-2,4-diensure2,3-DihydroxyfumarsureMesoweinsureHexa-2,4-diensure

Nachgelagerte Produkte

DiethyltartratDikaliumtartratDisodium tartrate dihydrateDikaliumbis[μ-[tartrato(4-)-O1,O2:O3,O4]]diantimonat(2-), stereoisomerDiammoniumtartratBrenztraubensureLeukomycin, [R-(R*,R*)]-2,3-Dihydroxybutandioat (Salz)KaliumnatriumtartratDiethyl-[S-(R*,R*)]-tartratKaliumhydrogentartratD-N-(4-Hydroxyphenyl)glycin
Ergänzende Hinweise · 1 Eintrag

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.