anhídrido 1,2,4-bencenotricarboxílico - ≥97% , CAS No.552-30-7

CAS: 552-30-7 Cat. No.: B104832 Peso molecular: 192.13 Beilstein Registry Number: 9394 Número EC: 209-008-0

GRADE & PURITY ≥97%

Synonyms

1,4-Benzenetricarboxylic acid anhydride | Trimellitic anhydride treated hemoglobin | Trimellitic anhydride, purum, >=97.0% (T) | 1,2,4-Benzenetricarboxylic acid 1,2-anhydride | AC-811 | C0959 | NCGC00256953-01 | Trimellitic anhydride treated IgG | 1,3-Dio

Storage

Argón cargado

Shipped In

Normal

Descripción general

Descripción del producto

el anhídrido 1,2,4-bencenotricarboxílico (TA) es un monómero hidrófilo de uso polivalente; como agente de curado para resinas de base epoxi y como plastificante para cloruro de polivinilo (PVC).

Aplicación

El TA puede modificar químicamente el bagazo de caña de azúcar, que puede utilizarse en la absorción de colorantes de auramina y safranina a partir de soluciones acuosas. Puede mezclarse con propano epoxi en la síntesis de acrilatos de poliuretano, que pueden utilizarse como oligómeros para revestimientos de base ultravioleta. Las membranas de ultrafiltración de poliamida P84 pueden funcionalizarse con TA mediante la interacción de los enlaces amida con los anhídridos.

Specifications

Sinónimos

1, 4-Benzenetricarboxylic acid anhydride | Trimellitic anhydride treated hemoglobin | Trimellitic anhydride, purum, >=97.0% (T) | 1, 2, 4-Benzenetricarboxylic acid 1, 2-anhydride | AC-811 | C0959 | NCGC00256953-01 | Trimellitic anhydride treated IgG | 1, 3-Dio

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Argón cargado

Enviado en

Normal

Pureza

≥97%

Nombres e identificadores

• Sonrisas canónicas: C1=CC2=C(C=C1C(=O)O)C(=O)OC2=O
• IUPAC Name: 1,3-dioxo-2-benzofuran-5-carboxylic acid
• InChIKey: SRPWOOOHEPICQU-UHFFFAOYSA-N
• INCHI: 1S/C9H4O5/c10-7(11)4-1-2-5-6(3-4)9(13)14-8(5)12/h1-3H,(H,10,11)
• Isómeros SMILES: C1=CC2=C(C=C1C(=O)O)C(=O)OC2=O
• WGK Alemania: 1
• RTECS: DC2050000
• Peso molecular: 192.13
• Beilstein: 9394
• Reaxy-Rn: 9394
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9394&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Benzofurans
      • Subclass Benzofuranones

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Benzofurans
• Subclass: Benzofuranones
• Intermediate Tree Nodes: Not available
• Direct Parent: Phthalic anhydrides
• Alternative Parents: Isobenzofuranones Tricarboxylic acids and derivatives Benzenoids Carboxylic acid anhydrides Oxacyclic compounds Carboxylic acids Organooxygen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Phthalic anhydride - Phthalic_anhydride - Isobenzofuranone - Isocoumaran - Tricarboxylic acid or derivatives - Benzenoid - Carboxylic acid anhydride - Oxacycle - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phthalic anhydrides. These are compounds containing a phthalic anhydride moiety (or a derivative thereof), which consists of a benzene fused to a furan-1,3-dione.
• External Descriptors: 2-benzofurans - dioxo monocarboxylic acid - cyclic dicarboxylic anhydride

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 (no humanos)

Botrytis cinerea (4183 Activities)

Explore this target

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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Hydrolyzes in water. Soluble in ethanol, acetone, and most other organic solvents.
• Sensibilidad: moisture sensitive
• Punto de inflamación (°F): 227℃
• Punto de inflamación (°C): 227℃
• Punto de ebullición (°C): 240-245°C
• Punto de fusión (°C): 161-163.5°C
• Peso molecular: 192.120 g/mol
• XLogP3: 0.800
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 1
• Exact Mass: 192.006 Da
• Monoisotopic Mass: 192.006 Da
• Topological Polar Surface Area: 80.700 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 308.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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

Referencias

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