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Merck
CN

T400

DL -酒石酸

ReagentPlus®, 99%

别名:

DL-2,3-二羟基丁二酸

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线性分子式:
HOOC(CHOH)2COOH
化学文摘社编号:
133-37-9
分子量:
150.09
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24900184
EC Number:
205-105-7
Beilstein/REAXYS Number:
1725148
MDL number:
MFCD00071626

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产品名称

DL -酒石酸, ReagentPlus®, 99%

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

200

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相关类别

Application

DL-酒石酸的应用示例：
  • 在Debus–Radziszewski反应中作为弱酸，用于合成咪唑类离子液体。
  • 作为电化学沉积技术的添加剂，用于合成X射线吸收用的铋薄膜。
  • 作为合成氧化铟锡(ITO)纳米晶体粉末的络合剂。
  • 作为氧化聚合法合成聚苯胺纳米纤维和纳米管的掺杂剂。

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H318

Hazard Classifications

Eye Dam. 1

存储类别

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000507779
0000507779
0000499116
0000499120
0000499120

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  1. Which document(s) contains shelf-life or expiration date information for a given product?

    If available for a given product, the recommended re-test date or the expiration date can be found on the Certificate of Analysis.

  2. How do I get lot-specific information or a Certificate of Analysis?

    The lot specific COA document can be found by entering the lot number above under the "Documents" section.

  3. How do I find price and availability?

    There are several ways to find pricing and availability for our products. Once you log onto our website, you will find the price and availability displayed on the product detail page. You can contact any of our Customer Sales and Service offices to receive a quote.  USA customers:  1-800-325-3010 or view local office numbers.

  4. What is the naturally occurring form of tartaric acid?

    The natural form of tartaric acid is L-(+)-tartaric acid.

  5. How is Product T400, DL-Tartaric acid, used?

    Tartaric acid is used in the organic synthesis of chiral molecules.

  6. 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.

  7. 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. 

  8. My question is not addressed here, how can I contact Technical Service for assistance?

    Ask a Scientist here.

Green Imidazolium Ionics-From Truly Sustainable Reagents to Highly Functional Ionic Liquids.
Troger-M?ller S, et al.
Chemistry?A European Journal , 23(49), 11810-11817 (2017)
Transparent and conducting ITO thin films by spin coating of an aqueous precursor solution.
Sunde TOL, et al.
Journal of Materials Chemistry, 22(31), 15740-15749 (2012)
The unique role of DL-tartaric acid in determining the morphology of polyaniline nanostructures during an interfacial oxidation polymerization.
Sun Q and Deng Y
Materials Letters, 62(12-13), 1831-1834 (2008)
Microstructure and electrical transport in electrodeposited Bi films.
Moral-Vico J, et al.
Journal of Electroanalytical Chemistry, 832(49), 40-47 (2019)
Anne Toboldt et al.
Applied and environmental microbiology, 78(20), 7347-7357 (2012-08-14)
In this study, the population structure, incidence, and potential sources of human infection caused by the d-tartrate-fermenting variant of Salmonella enterica serovar Paratyphi B [S. Paratyphi B (dT+)] was investigated. In Germany, the serovar is frequently isolated from broilers. Therefore
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