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27506

Sigma-Aldrich

L-(+)-Tartaric acid

puriss., meets analytical specification of Ph. Eur., NF, 99.7-100.5% (calc. to the dried substance), powder

Synonyme(s) :

(2R,3R)-(+)-Tartaric acid, L-Threaric acid

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About This Item

Formule linéaire :
HO2CCH(OH)CH(OH)CO2H
Numéro CAS:
87-69-4
Poids moléculaire :
150.09
Numéro Beilstein :
1725147
Numéro CE :
201-766-0
Numéro MDL:
MFCD00064207
Code UNSPSC :
12352106
ID de substance PubChem :
57648257
Nomenclature NACRES :
NA.25

Densité de vapeur

5.18 (vs air)

Niveau de qualité

200

Qualité

puriss.
meets analytical specification of Ph. Eur., NF

Pureté

99.7-100.5% (calc. to the dried substance)

Forme

powder

Activité optique

[α]20/D +12.0 to +12.8°, c = 20% in H2O

Température d'inflammation spontanée

797 °F

Impuretés

organic volatile impurities, complies (GC)
 residual solvents, complies
≤0.001% heavy metals (as Pb)

Résidus de calcination

≤0.05% (as SO4)

Perte

≤0.2% loss on drying, 105 °C

Pf

168-170 °C
170-172 °C (lit.)

Solubilité

water: soluble 150 g/L at 20 °C

Traces d'anions

chloride (Cl-): ≤100 mg/kg
oxalate (C2O42-): in accordance
oxalate (as oxalic acid): ≤100 mg/kg
sulfate (SO42-): ≤100 mg/kg

Traces de cations

As: ≤2 mg/kg
Ca: ≤200 mg/kg
Cu: ≤10 mg/kg
Hg: ≤1 mg/kg
Pb: ≤2 mg/kg
Zn: ≤10 mg/kg

Adéquation

complies for appearance of solution

Application(s)

pharmaceutical (small molecule)

Chaîne SMILES 

O[C@H]([C@@H](O)C(O)=O)C(O)=O

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-/m1/s1

Clé InChI

FEWJPZIEWOKRBE-JCYAYHJZSA-N

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Pictogrammes

Corrosion
GHS05

Mention d'avertissement

Danger

Mentions de danger

H318

Conseils de prudence

P280 - P305 + P351 + P338

Classification des risques

Eye Dam. 1

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

302.0 °F - closed cup

Point d'éclair (°C)

150 °C - closed cup

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

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Certificats d'analyse (COA)

Lot/Batch Number
BCCL4882
BCCK5654
BCCH4571
BCCG5572
BCCG0355

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M Alsina et al.
Blood, 87(4), 1495-1501 (1996-02-15)
Osteolytic bone destruction and its complications, bone pain, pathologic fractures, and hypercalcemia, are a major source of morbidity and mortality in patients with multiple myeloma. The bone destruction in multiple myeloma is due to increased osteoclast (OCL) activity and decreased
A A Cole et al.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 35(2), 203-206 (1987-02-01)
Tartrate-resistant acid phosphatase (TRAP) has been proposed as a cytochemical marker for osteoclasts. We have developed an improved technique for the localization of TRAP in rat and mouse bone and cartilage. This procedure employs JB-4 plastic as the embedding medium
J B Olivato et al.
Carbohydrate polymers, 92(2), 1705-1710 (2013-02-13)
Tartaric acid (TA), a dicarboxylic acid, can act as a compatibiliser in starch/polyester blends. A mixture design was proposed to evaluate the effect of TA on the properties of starch/poly (butylene adipate co-terephthalate) (PBAT) blown films plasticised with glycerol. The
Mrinal Kanti Bain et al.
Carbohydrate polymers, 91(2), 529-536 (2012-11-06)
Gelation temperature of MC was reduced from 59°C to 54°C with the addition of 10% PEG. Sodium tartrate (NaT) and sodium citrate (NaC) were added to the MC-PEG solution to further reduce the gelation temperature close to physiological temperature. Different
Mark D Eddleston et al.
Chemical communications (Cambridge, England), 48(92), 11340-11342 (2012-10-18)
The formation of diastereomeric cocrystals of malic acid and tartaric acid was investigated by liquid-assisted grinding in the solid state. We demonstrate that racemic malic acid can be converted into two distinct diastereomeric cocrystal phases by grinding with a single
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