o-Phthalaldehyde - for fluorescence analysis, ≥99%(HPLC) , CAS No.643-79-8

CAS: 643-79-8 Cat. No.: P108633 Fórmula: C₈H₆O₂ Peso molecular: 134.13 Beilstein Registry Number: 878317 Número CE: 211-402-2

GRADE & PURITY for Fluorescence analysis, ≥99%(HPLC)

Synonyms

OPA | 4-07-00-02138 (Beilstein Handbook Reference) | benzene-1,2-dicarbaldehyde | D03470 | NCGC00166206-02 | SCHEMBL33393 | DTXSID6032514 | o-Phthalic dicarboxaldehyde | Phthalaldialdehyde | 4P8QP9768A | Benzene-1,2-dicarboxakdehyde | NCGC00166206-04 | NS

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Visão geral

For precolumn derivatization of amino acids for HPLC separation. For flow cytometric measurements of protein thiol groups.

Specifications

Sinónimos

OPA | 4-07-00-02138 (Beilstein Handbook Reference) | benzene-1,2-dicarbaldehyde | D03470 | NCGC00166206-02 | SCHEMBL33393 | DTXSID6032514 | o-Phthalic dicarboxaldehyde | Phthalaldialdehyde | 4P8QP9768A | Benzene-1,2-dicarboxakdehyde | NCGC00166206-04 | NS

Especificações e pureza

for fluorescence analysis, ≥99%(HPLC)

Condições de armazenamento de armazenamento

Store at 2-8°C,Argon charged

Enviado em

Wet ice

Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.

Grau

for Fluorescence analysis

Pureza

≥99%(HPLC)

Nomes e identificadores

Pubchem Sid

508816716

Sorrisos canónicos

C1=CC=C(C(=C1)C=O)C=O

IUPAC Name

phthalaldehyde

InChIKey

ZWLUXSQADUDCSB-UHFFFAOYSA-N

INCHI

1S/C8H6O2/c9-5-7-3-1-2-4-8(7)6-10/h1-6H

SMILES isoméricas

C1=CC=C(C(=C1)C=O)C=O

WGK Alemanha

3

RTECS

TH6950000

Número UN

2923

Grupo de embalagem

II

Peso molecular

134.13

Beilstein

878317

Reaxy-Rn

878317

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=878317&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Benzoyl derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Benzoyl derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzoyl derivatives
• Alternative Parents: Benzaldehydes Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Benzoyl - Benzaldehyde - Aryl-aldehyde - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aldehyde - Aromatic homomonocyclic compound
• Descrição: This compound belongs to the class of organic compounds known as benzoyl derivatives. These are organic compounds containing an acyl moiety of benzoic acid with the formula (C6H5CO-).
• External Descriptors: benzaldehydes - dialdehyde

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

Alvos associados (humanos)

VDR Tclin Vitamin D receptor (26531 Activities)

Discover Target: VDR

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THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)

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POLK Tbio DNA polymerase kappa (8653 Activities)

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EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

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TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

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LMNA Tbio Prelamin-A/C (36751 Activities)

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BLM Tchem Bloom syndrome protein (4248 Activities)

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GMNN Tbio Geminin (128009 Activities)

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PMP22 Tbio Peripheral myelin protein 22 (699 Activities)

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KMT2A Tchem Histone-lysine N-methyltransferase MLL (17327 Activities)

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USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)

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MEN1 Tchem Menin/Histone-lysine N-methyltransferase MLL (48157 Activities)

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Alvos associados (não humanos)

Mycobacteroides chelonae (540 Activities)

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Meloidogyne incognita (862 Activities)

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Mus musculus (284745 Activities)

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GCN5 Histone acetyltransferase GCN5 (89 Activities)

Discover Target: GCN5

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ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)

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Mecanismos de ação

Propriedades químicas e físicas

• Sensibilidade: Air,Light and Moisture Sensitive
• Ponto de inflamação (°F): 269.6 °F
• Ponto de inflamação (°C): >110℃
• Ponto de ebulição (°C): 84°C/0.8mmHg
• Ponto de fusão (°C): 56-57°C
• Peso molecular: 134.130 g/mol
• XLogP3: 1.200
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 134.037 Da
• Monoisotopic Mass: 134.037 Da
• Topological Polar Surface Area: 34.100 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 115.000
• 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