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(+)-Dibenzoyl-D-tartaric Acid - >98.0%(HPLC), high purity , CAS No.17026-42-5

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(+)-Dibenzoyl-D-tartaric Acid - >98.0%(HPLC), high purity , CAS No.17026-42-5

COA

Grade & Purity:

≥98%(HPLC)

Cas Number: 17026-42-5
Molecular Weight: 358.3
Beilstein Registry Number: 2227340
MDL number: MFCD00063222
PubChem CID: 1550213
PubChem SID: 504760595

In stock

Item Number

D154781

Grouped product items
SKU	Size	Availability	Price
D154781-25g	25g	2	$18.90
D154781-100g	100g	1	$64.90
D154781-250g	250g	2	$82.90
D154781-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$148.90

View related series

asymmetric synthesis (590) carboxylic acid (2098)

Basic Description

Synonyms	D-(+)-Di-O,O-benzoyltartaric acid \| D3826 \| (2S,3S)-2,3-dibenzoyloxybutanedioic acid \| Dibenzoyltartaric acid, (+)-D- \| (+)-Dibenzoyl-D-tartaric acid, anhydrous \| Dibenzoyl-D-tartaric acid \| (2S,3S)-2,3-bis(benzoyloxy)succinic acid \| (+)-2,3-Dibenzoyl-D-t
Specifications & Purity	≥98%(HPLC)
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	(+)-2,3-Dibenzoyl-D-tartaric acid is an acidic chiral resolving reagent[4] for the resolution of bases Reagent for chiral resolution of amino compounds.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Carboxylic acids and derivatives
    - Subclass Tetracarboxylic acids and derivatives

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Carboxylic acids and derivatives
Subclass	Tetracarboxylic acids and derivatives
Intermediate Tree Nodes	Not available
Direct Parent	Tetracarboxylic acids and derivatives
Alternative Parents	Benzoic acid esters Benzoyl derivatives Monosaccharides Carboxylic acid esters Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Tetracarboxylic acid or derivatives - Benzoate ester - Benzoic acid or derivatives - Benzoyl - Benzenoid - Monosaccharide - Monocyclic benzene moiety - Carboxylic acid ester - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(non-human)

Influenza A virus (11224 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	504760595
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504760595
IUPAC Name	(2S,3S)-2,3-dibenzoyloxybutanedioic acid
INCHI	InChI=1S/C18H14O8/c19-15(20)13(25-17(23)11-7-3-1-4-8-11)14(16(21)22)26-18(24)12-9-5-2-6-10-12/h1-10,13-14H,(H,19,20)(H,21,22)/t13-,14-/m0/s1
InChIKey	YONLFQNRGZXBBF-KBPBESRZSA-N
Smiles	C1=CC=C(C=C1)C(=O)OC(C(C(=O)O)OC(=O)C2=CC=CC=C2)C(=O)O
Isomeric SMILES	C1=CC=C(C=C1)C(=O)O[C@@H]([C@@H](C(=O)O)OC(=O)C2=CC=CC=C2)C(=O)O
WGK Germany	3
Molecular Weight	358.3
Beilstein	2227340
Reaxy-Rn	2227342
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2227342&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

12 results found

Lot Number	Certificate Type	Date	Item
H1730044	Certificate of Analysis	Mar 04, 2025	D154781
I2003125	Certificate of Analysis	Jun 13, 2024	D154781
B2301372	Certificate of Analysis	Nov 26, 2022	D154781
B2301373	Certificate of Analysis	Nov 26, 2022	D154781
F2414088	Certificate of Analysis	Nov 26, 2022	D154781
B2301374	Certificate of Analysis	Nov 26, 2022	D154781
B2301375	Certificate of Analysis	Nov 26, 2022	D154781
B2301376	Certificate of Analysis	Nov 26, 2022	D154781
B2301369	Certificate of Analysis	Nov 26, 2022	D154781
B2301370	Certificate of Analysis	Nov 26, 2022	D154781
B2301371	Certificate of Analysis	Nov 26, 2022	D154781
I2308217	Certificate of Analysis	Nov 04, 2021	D154781

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Chemical and Physical Properties

Solubility	Soluble in ethanol. Insoluble in water.
Sensitivity	Hygroscopic
Specific Rotation[α]	117° (C=1,EtOH)
Melt Point(°C)	152.0 to 156.0 °C
Molecular Weight	358.300 g/mol
XLogP3	2.600
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	8
Rotatable Bond Count	9
Exact Mass	358.069 Da
Monoisotopic Mass	358.069 Da
Topological Polar Surface Area	127.000 Å²
Heavy Atom Count	26
Formal Charge	0
Complexity	483.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	2
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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