D(-)-Tartaric acid
- CAS No.
- 526-83-0
- Chemical Name:
- D(-)-Tartaric acid
- Synonyms
- (2R,3S)-2,3-Dihydroxybernsteinsaeure;(2R,3R)-2,3-Dihydroxybernsteinsaeure;L-tartaricaci;D-2,3-Dihydroxysuccinic acid;Acacia senegal、Acacia seyal;D(-)-Tartaric acid;Tartaric Acid Impurity 6;D(-)-Tartaric acid, 98%+;Dihydroxybernsteinsaeure;high quality D(-)-Tartaric acid
- CBNumber:
- CB6663151
- Molecular Formula:
- C4H6O6
- Molecular Weight:
- 150.09
- MOL File:
- 526-83-0.mol
- MSDS File:
- SDS
- Modify Date:
- 2024/6/22 7:31:40
| Melting point | 159-171°C |
|---|---|
| Boiling point | 399.3±42.0 °C(Predicted) |
| Density | 1.886±0.06 g/cm3(Predicted) |
| storage temp. | Sealed in dry,Room Temperature |
| solubility | DMSO (Slightly, Heated), Methanol (Slightly), Water (Sparingly, Sonicated) |
| form | Solid |
| pka | 3.07±0.34(Predicted) |
| color | White to Off-White |
| Odor | at 100.00 %. odorless |
| Odor Type | odorless |
| InChI | InChI=1S/C4H6O6/c5-1(3(7)8)2(6)4(9)10/h1-2,5-6H,(H,7,8)(H,9,10) |
| InChIKey | FEWJPZIEWOKRBE-UHFFFAOYSA-N |
| SMILES | C(O)(=O)C(O)C(O)C(O)=O |
| LogP | -1.081 (est) |
| EPA Substance Registry System | 2,3-Dihydroxysuccinic acid (526-83-0) |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |  GHS07 |
|---|---|
| Signal word | Warning |
| Hazard statements | H315-H319 |
| Precautionary statements | P305+P351+P338 |
| HS Code | 29181200 |
D(-)-Tartaric acid Chemical Properties,Uses,Production
Description
Tartaric acid is a white crystalline diprotic aldaric acid. It occurs naturally in many plants, particularly grapes, bananas, and tamarinds, is commonly combined with baking soda to function as a leavening agent in recipes, and is one of the main acids found in wine. It is added to other foods to give a sour taste, and is used as an antioxidant. Salts of tartaric acid are known as tartrates. It is a dihydroxyl derivative of succinic acid.
Tartaric acid was first isolated from potassium tartrate, known to the ancients as tartar, circa 800 AD, by the alchemist Jabir ibn Hayyan The modern process was developed in 1769 by the Swedish chemist Carl Wilhelm Scheele.
Tartaric acid played an important role in the discovery of chemical chirality. This property of tartaric acid was first observed in 1832 by Jean Baptiste Biot, who observed its ability to rotate polarized light. Louis Pasteur continued this research in 1847 by investigating the shapes of ammonium sodium tartrate crystals, which he found to be chiral. By manually sorting the differently shaped crystals under magnification, Pasteur was the first to produce a pure sample of levotartaric acid.
Uses
Pharmaceutic aid (buffering agent).
Definition
A crystalline naturallyoccurring carboxylic acid,(CHOH)2(COOH)2; r.d. 1.8; m.p.171–174°C. It can be obtained fromtartar (potassium hydrogen tartrate)deposits from wine vats, and is usedin baking powders and as a foodstuffsadditive. The compound isoptically active (see optical activity).The systematic name is 2,3-dihydroxybutanedioic acid.
D(-)-Tartaric acid Preparation Products And Raw materials
Raw materials
Preparation Products
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