BAPTA-TMFM (Calcium Ion Fluorescent Chelating Indicator) - BioReagent, Biological Stain, for fluorescence analysis, for microscopy, ≥96% , CAS No.96315-11-6

CAS: 96315-11-6 Cat. No.: B1454644 Formule: C₂₈H₃₄N₂O₁₁ Poids moléculaire: 574.58

GRADE & PURITY BioReagent, Biological Stain, for Fluorescence analysis, for Microscopy, ≥96%

Synonyms

BAPTA-TMFM | Tetramethyl 5-Formyl-5'-Methyl Bis-(2-Aminophenoxymethylene)-N,N,N',N'-Tetraacetate | Dimethyl 2,2'-((2-(2-(2-(bis(2-methoxy-2-oxoethyl)amino)-5-formylphenoxy)ethoxy)-4-methylphenyl)azanediyl)diacetate

Storage

Protected from light,Store at -20°C,Avoid repeated freezing and thawing

Shipped In

Ice chest + Ice pads

Application

Cell Staining‌, Fluorescence Analysis

Vue d’ensemble

BAPTA-TMFM (Calcium Ion Fluorescent Chelating Indicator) is a fluorescent chelating indicator used to study the role of cytosolic free calcium.

Specifications

Synonymes

BAPTA-TMFM | Tetramethyl 5-Formyl-5'-Methyl Bis-(2-Aminophenoxymethylene)-N,N,N',N'-Tetraacetate | Dimethyl 2,2'-((2-(2-(2-(bis(2-methoxy-2-oxoethyl)amino)-5-formylphenoxy)ethoxy)-4-methylphenyl)azanediyl)diacetate

Spécifications et pureté

BioReagent, Biological Stain, for fluorescence analysis, for microscopy, ≥96%

Stabilité et stockage

Store at -20℃ long term (12 months). Store in the dark. Avoid freeze/thaw cycle.

Conditions de stockage de stockage

Protected from light,Store at -20°C,Avoid repeated freezing and thawing

Expédié en

Ice chest + Ice pads

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Grade

Biological Stain, BioReagent, pour l'analyse par fluorescence, pour la microscopie

Pureté

≥96%

Noms et identifiants

• Sourires canoniques: CC1=CC(=C(C=C1)N(CC(=O)OC)CC(=O)OC)OCCOC2=C(C=CC(=C2)C=O)N(CC(=O)OC)CC(=O)OC
• IUPAC Name: methyl 2-[2-[2-[2-[bis(2-methoxy-2-oxoethyl)amino]-5-formylphenoxy]ethoxy]-N-(2-methoxy-2-oxoethyl)-4-methylanilino]acetate
• InChIKey: GKTVRWOCZLYLJV-UHFFFAOYSA-N
• INCHI: 1S/C28H34N2O11/c1-19-6-8-21(29(14-25(32)36-2)15-26(33)37-3)23(12-19)40-10-11-41-24-13-20(18-31)7-9-22(24)30(16-27(34)38-4)17-28(35)39-5/h6-9,12-13,18H,10-11,14-17H2,1-5H3
• Isomères SMILES: CC1=CC(=C(C=C1)N(CC(=O)OC)CC(=O)OC)OCCOC2=C(C=CC(=C2)C=O)N(CC(=O)OC)CC(=O)OC
• Poids moléculaire: 574.58

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Tetracarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Tetracarboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Tetracarboxylic acids and derivatives
• Alternative Parents: Alpha amino acid esters Aminophenyl ethers Phenoxy compounds Dialkylarylamines Benzoyl derivatives Benzaldehydes Aniline and substituted anilines Aminotoluenes Alkyl aryl ethers Methyl esters Organopnictogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Alpha-amino acid ester - Tetracarboxylic acid or derivatives - Alpha-amino acid or derivatives - Aminophenyl ether - Phenoxy compound - Benzaldehyde - Benzoyl - Phenol ether - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Aniline or substituted anilines - Aminotoluene - Aryl-aldehyde - Toluene - Alkyl aryl ether - Benzenoid - Monocyclic benzene moiety - Methyl ester - Tertiary amine - Amino acid or derivatives - Carboxylic acid ester - Ether - Organopnictogen compound - Carbonyl group - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Aldehyde - Amine - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups.
• External Descriptors: Not available

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

Propriétés chimiques et physiques

• Sensibilité: Light-sensitive