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 Molecular Weight: 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

Overview

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

Specifications

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

Specifications & Purity

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

Stability And Storage

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

Storage

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

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Grade

Biological Stain, BioReagent, for Fluorescence analysis, for Microscopy

Purity

≥96%

Names and Identifiers

• Canonical 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
• 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
• Isomeric 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
• Molecular Weight: 574.58

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: 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

Chemical and Physical Properties

• Sensitivity: Light-sensitive