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

≥98%(HPLC)

CAS#: 17026-42-5
Formula: C₁₈H₁₄O₈
Molecular Weight: 358.3
Beilstein Registry Number: 2227340
MDL number: MFCD00063222
PubChem CID: 1550213

Item Number

D154781

Grouped product items
SKU	Size	Availability	Price
D154781-25g	25g	In stock	$18.90
D154781-100g	100g	In stock	$64.90
D154781-250g	250g	In stock	$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 carboxylic acid

Basic Description

Synonyms	17026-42-5\|Dibenzoyl-D-tartaric acid\|(+)-Dibenzoyl-D-tartaric acid\|Butanedioic acid, 2,3-bis(benzoyloxy)-, (2S,3S)-\|(2S,3S)-2,3-bis(benzoyloxy)succinic acid\|(+)-2,3-Dibenzoyl-D-tartaric acid\|D-Dibenzoyltartaric acid\|(+)-Dibenzoyltartaric acid\|(+)-O,O-Dibe
Specifications & Purity	>98.0%(HPLC)
Storage Temp	Store at 2-8°C
Shipped In	Wet ice
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.

Names and Identifiers

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
InChi Key	YONLFQNRGZXBBF-KBPBESRZSA-N
Canonical 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
PubChem CID	1550213
Molecular Weight	358.3
Beilstein	2227340
Reaxy-Rn	2227343

Certificates

Certificate of Analysis(COA)

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11 results found

Lot Number	Certificate Type	Date	Item
I2003125	Certificate of Analysis	Jun 13, 2024	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
B2301372	Certificate of Analysis	Nov 26, 2022	D154781
B2301373	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
F2414088	Certificate of Analysis	Nov 26, 2022	D154781
I2308217	Certificate of Analysis	Nov 04, 2021	D154781

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

Safety and Hazards(GHS)

Pictogram(s)	GHS07
Signal	Warning
Hazard Statements	H319:Causes serious eye irritation
Precautionary Statements	P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing. P280:Wear protective gloves/protective clothing/eye protection/face protection. P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes. P337+P317:If eye irritation persists: Get medical help.
WGK Germany	3
Reaxy-Rn	2227343

References

1. Lavielle G, Hautefaye P, Schaeffer C, Boutin JA, Cudennec CA, Pierré A. (1991) New alpha-amino phosphonic acid derivatives of vinblastine: chemistry and antitumor activity.. J Med Chem, 34 (7): (1998-2003). [PMID:2066973]
2. Emily M Jutkiewicz,Erik B Eller,John E Folk,Kenner C Rice,John R Traynor,James H Woods. (2004-01-15) Delta-opioid agonists: differential efficacy and potency of SNC80, its 3-OH (SNC86) and 3-desoxy (SNC162) derivatives in Sprague-Dawley rats.. The Journal of pharmacology and experimental therapeutics, 309 ((1)): (173-181). [PMID:14722329]
3. Yan-Song Zheng,Chun Zhang. (2004-04-09) Exceptional chiral recognition of racemic carboxylic acids by calix[4]arenes bearing optically pure alpha,beta-amino alcohol groups.. Organic letters, 6 ((8)): (1189-1192). [PMID:15070294]
4. Mirjan M van Timmeren,Stephan J L Bakker,Coen A Stegeman,Rijk O B Gans,Harry van Goor. (2005-09-08) Addition of oleic acid to delipidated bovine serum albumin aggravates renal damage in experimental protein-overload nephrosis.. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 20 ((11)): (2349-2357). [PMID:16144858]
5. Christian Zimmer,Tanja Platz,Neza Cadez,Friedrich Giffhorn,Gert-Wieland Kohring. (2006-07-19) A cold active (2R,3R)-(-)-di-O-benzoyl-tartrate hydrolyzing esterase from Rhodotorula mucilaginosa.. Applied microbiology and biotechnology, 73 ((1)): (132-140). [PMID:16847603]
6. Yan-Song Zheng,Ao Ji,Xian-Jie Chen,Jin-Lan Zhou. (2007-11-21) Enantioselective nanofiber-spinning of chiral calixarene receptor with guest.. Chemical communications (Cambridge, England), ((32)(32)): (3398-3400). [PMID:18019510]
7. Jin-Lan Zhou,Xian-Jie Chen,Yan-Song Zheng. (2007-12-07) Heat-set gels and egg-like vesicles using two component gel system based on chiral calix[4]arenes.. Chemical communications (Cambridge, England), ((48)(48)): (5200-5202). [PMID:18060141]
8. Jianghong An,Davy C W Lee,Anna H Y Law,Cindy L H Yang,Leo L M Poon,Allan S Y Lau,Steven J M Jones. (2009-05-08) A novel small-molecule inhibitor of the avian influenza H5N1 virus determined through computational screening against the neuraminidase.. Journal of medicinal chemistry, 52 ((9)): (2667-2672). [PMID:19419201]
9. Feipeng Jiao,Weijie Yang,Fen Wang,Lingxing Tian,Lin Li,Xiaoqing Chen,Kelang Mu. (2012-06-02) Enantioseparation of racemic mixtures based on solvent sublation.. Chirality, 24 ((8)): (661-667). [PMID:22653806]
10. Stanley I Goldberg. (2013-01-25) A laboratory model of a prebiotic, spontaneous, and continuous enantiomeric enrichment process.. Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life, 43 ((1)): (31-37). [PMID:23344885]
11. C Q Cao,Y Hong,A Dray,M Perkins. (2001-05-04) Spinal delta-opioid receptors mediate suppression of systemic SNC80 on excitability of the flexor reflex in normal and inflamed rat.. European journal of pharmacology, 418 ((1-2)): (79-87). [PMID:11334868]

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