D-(-)-Tartaric acid - 10mM in DMSO , CAS No.147-71-7

CAS: 147-71-7 Cat. No.: D421725 Fórmula: C₄H₆O₆ Peso molecular: 150.09 Beilstein Registry Number: 1725145 Número EC: 205-695-6

GRADE & PURITY 10mM in DMSO

Synonyms

(2R/S,3R/S)-dihydroxy-1,4-butanedioic acid | AM20080237 | DL-Tartaric acid, >=99% | s3134 | (S,S)-Tartaric acid;Tartaric acid;D-(-)-Tartaric acid | Butanedioic acid, 2,3-dihydroxy-, (S-(R*,R*))- | (2s, 3s)-tartaric acid | Acetamide, N-(5,6,7,8-tetrahydro-

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Descripción general

D-(-)-Tartaric acid is a polyhydroxy acid. Oxidation of d-tartaric acid has been reported.Crystal structure of D-(-)-tartaric acid has been studied by X-ray and neutron diffraction.Tartaric acid is reported to be one of the constituents of soy bean Lipositol.Tartaric acid assists in the generation Y2O3:Eu3+ nanoparticles by solgel method.Tartaric acid is the main acid present in grapes and red wine.
D-(-)-Tartaric acid may be used in the synthesis of the HIV-protease inhibitor nelfinavir.It may be used in the synthesis of chiral aziridine derivative, a common intermediate for the synthesis of hydroxyethylamine class HIV protease inhibitors such as saquinavir, amprenavir, or nelfinavir.

product description：

Tartaric acid is a polyhydroxy acid with wide applications in the textile, pharma, and food industries. It is commonly used as a food additive and acts as an antioxidant and acidification agent. It is also used as a starting material for the preparation of many bioactive molecules.

application：

D-(-)-Tartaric acid is used as a resolving agent in organic synthesis. It is used as a precursor for the preparation of its ester derivatives like D-tartaric acid diethyl ester, D-tartaric acid dimethyl ester and D-tartaric acid diiso-propyl ester. It finds application in the synthesis of chiral aziridine derivative, a common intermediate for the preparation of hydroxyethylamine class HIV protease inhibitors viz. as saquinavir, amprenavir and nelfinavir. It is widely used in the food industry as a beer foaming agent, for food acidity regulations and as a flavoring agent.

Specifications

Sinónimos

(2R/S,3R/S)-dihydroxy-1,4-butanedioic acid | AM20080237 | DL-Tartaric acid, >=99% | s3134 | (S,S)-Tartaric acid;Tartaric acid;D-(-)-Tartaric acid | Butanedioic acid, 2,3-dihydroxy-, (S-(R*,R*))- | (2s, 3s)-tartaric acid | Acetamide, N-(5,6,7,8-tetrahydro-

Especificaciones y pureza

10mM in DMSO

Condiciones de almacenamiento de almacenamiento

Store at -80°C

Enviado en

Dry ice packs + Cold packs

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Nombres e identificadores

Pubchem Sid

528763996

Sonrisas canónicas

C(C(C(=O)O)O)(C(=O)O)O

IUPAC Name

(2S,3S)-2,3-dihydroxybutanedioic acid

InChIKey

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

Isómeros SMILES

[C@H]([C@@H](C(=O)O)O)(C(=O)O)O

WGK Alemania

3

RTECS

WW7875000

Peso molecular

150.09

Beilstein

1725145

Reaxy-Rn

510169

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=510169&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Not available
• Direct Parent: Sugar acids and derivatives
• Alternative Parents: Short-chain hydroxy acids and derivatives Beta hydroxy acids and derivatives Monosaccharides Fatty acids and conjugates Dicarboxylic acids and derivatives Alpha hydroxy acids and derivatives Secondary alcohols 1,2-diols Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Beta-hydroxy acid - Short-chain hydroxy acid - Sugar acid - Monosaccharide - Hydroxy acid - Dicarboxylic acid or derivatives - Alpha-hydroxy acid - Fatty acid - Secondary alcohol - 1,2-diol - Carboxylic acid - Carboxylic acid derivative - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as sugar acids and derivatives. These are compounds containing a saccharide unit which bears a carboxylic acid group.
• External Descriptors: tartaric acid

Data sources

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

Objetivos asociados (humanos)

TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)

Discover Target: TSHR

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

CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)

Discover Target: CYP2D6

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

CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)

Discover Target: CYP1A2

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

CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)

Discover Target: CYP2C9

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

CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)

Discover Target: CYP2C19

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

CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

Discover Target: CYP3A4

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MT2 (2907 Activities)

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

KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)

Discover Target: KDM4A

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

Objetivos asociados (no humanos)

pol Human immunodeficiency virus type 1 integrase (9041 Activities)

Discover Target: pol

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

HD1 Histone deacetylase (38 Activities)

Discover Target: HD1

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

Human immunodeficiency virus 1 (70413 Activities)

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Mecanismos de acción

Propiedades químicas y físicas

• Sensibilidad: Light Sensitive
• Rotación específica [α]: -12.5 ° (C=5, H2O)
• Punto de inflamación (°F): 410°F
• Punto de inflamación (°C): 210℃
• Punto de fusión (°C): 166-170°C
• Peso molecular: 150.090 g/mol
• XLogP3: -1.900
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 3
• Exact Mass: 150.016 Da
• Monoisotopic Mass: 150.016 Da
• Topological Polar Surface Area: 115.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 134.000
• 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