Ácido (-)-dibenzoil- D-tartárico monohidrato, 99 %, Thermo Scientific Chemicals
Ácido (-)-dibenzoil- D-tartárico monohidrato, 99 %, Thermo Scientific Chemicals
Ácido (-)-dibenzoil- D-tartárico monohidrato, 99 %, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Ácido (-)-dibenzoil- D-tartárico monohidrato, 99 %, Thermo Scientific Chemicals

CAS: 80822-15-7 | C18H16O9 | 376.32 g/mol
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Cantidad:
25 g
100 g
Número de catálogo A16503.22
también denominado A16503-22
Precio (EUR)
120,00
Each
Cantidad:
100 g
Pedido a granel o personalizado
Precio (EUR)
120,00
Each
Identificadores químicos
CAS80822-15-7
IUPAC Name(2S,3S)-2,3-bis(benzoyloxy)butanedioic acid hydrate
Molecular FormulaC18H16O9
InChI KeyDXDIHODZARUBLA-DZWQFRRJNA-N
SMILESO.OC(=O)[C@@H](OC(=O)C1=CC=CC=C1)[C@H](OC(=O)C1=CC=CC=C1)C(O)=O
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EspecificacionesSpecification SheetHoja de especificaciones
Appearance (Color)White
Melting Point (clear melt)86.0-92.0?C
Optical Rotation109.5 ± 0.1? (c=2 in EtOH)
FormPowder
Water Content (Karl Fischer Titration)2.45-7.01% (0.5-1.5 waters)
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(+)-Dibenzoyl-D-tartaric acid monohydrate is used as a chiral separation and racemization agent for amines. It is also used as a pharmaceutical raw material.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
(+)-Dibenzoyl-D-tartaric acid monohydrate is used as a chiral separation and racemization agent for amines. También se utiliza como materia prima farmacéutica.

Solubilidad
Soluble en metanol. Ligeramente soluble en agua.

Notas
incompatible con agentes oxidantes fuertes, bases y ácidos fuertes.
RUO – Research Use Only

General References:

  1. Chavakula, R.; Mutyala, N. R.; Chennupati, S. R. Industrially Viable Preparation of (R)-3-Quinuclidinol, a Key Building Block of Muscarine M1, M3 Agonists and M3 Antagonists. Org. Prep. Proced. Int. 2013, 45 (6), 507-509.
  2. Gizur, T.; Fogassy, E.; Balint, J.; Egri, G.; Törley, J.; Demeter, A.; Greiner, I. New practical synthesis of Tamsulosin. Chirality 2008, 20 (6), 790-795.