T400
DL-Tartaric acid
ReagentPlus®, 99%
Sinónimos:
DL-2,3-Dihydroxybutanedioic acid
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InChI key
FEWJPZIEWOKRBE-LWMBPPNESA-N
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
SMILES string
O[C@@H]([C@H](O)C(O)=O)C(O)=O
product line
ReagentPlus®
assay
99%
mp
210-212 °C (lit.)
Quality Level
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Categorías relacionadas
Application
- 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.
Legal Information
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 3
flash_point_f
410.0 °F - closed cup
flash_point_c
210 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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If available for a given product, the recommended re-test date or the expiration date can be found on the Certificate of Analysis.
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The lot specific COA document can be found by entering the lot number above under the "Documents" section.
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What is the naturally occurring form of tartaric acid?
The natural form of tartaric acid is L-(+)-tartaric acid.
How is Product T400, DL-Tartaric acid, used?
Tartaric acid is used in the organic synthesis of chiral molecules.
As the racemic form, how can Product T400, DL-Tartaric acid, also be listed?
Product T400, racemic tartaric acid, can also be listed as DL-(S,S/R,R)-(±)-tartaric acid.
What is the Department of Transportation shipping information for this product?
Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.
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