Triethanolamine, min. 99 %, for synthesis, 1 l, plastic

Catalog nr. 6300.1
Carl Roth

Volume: 1 liter
Value Packs: 1 piece
Price:
Sale price€36,05
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Description

Triethanolamine is an organic amino alcohol of minimum 99 % purity for synthesis, with empirical formula C₆H₁₅NO₃ and CAS number 102-71-6. The molar mass is 149,19 g/mol and the density is 1,12 g/cm³; the boiling point is 360 °C and the flash point is 190 °C. This grade is EG number 203-049-8 identifies the substance under European inventory listing. Triethanolamine from manufacturer Carl ROTH is positioned for use where a high-assay liquid reagent is required in preparative and synthetic workflows, including contexts linked to biological buffer reagent categories. Physical data such as density and thermal properties support handling and process planning in the laboratory. The material is offered as a defined synthesis-quality product so that laboratories can match purity and pack format to their protocols without ambiguity regarding identity or key physicochemical parameters.

Key features

  • Assay (GC): ≥99 %
  • Water: ≤0,1 %
  • Colour number (APHA): ≤30
  • Diethanolamine (GC): ≤0,4 %
  • 2-Aminoethanol (GC): ≤0,1 %
  • Highly boiling matter (GC): ≤0,5 %
  • CAS number: 102-71-6
  • Pack sizes: 1 l, 10 l, 2.5 l
  • EG nr.: 203-049-8
  • Purity: min. 99 %
  • Empirical formula: C₆H₁₅NO₃
  • Molar mass: 149,19 g/mol
  • Technical Information Sheet: PDF
  • Safety Data Sheet: PDF

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What is this article?

Triethanolamine, min. 99 %, for synthesis, 1 l, plastic is the article on this page. Luminix Health distributes Carl Roth for laboratory use. It sits in Protein biology (other), inside Protein biology & Western blot, in Life Science & Microbiology.

This shelf is the protein-biology article that is not a membrane and not an extraction kit: stains for gels, buffers, small tools of a protein bench. The method, a gel stain or a quantitation assay, still chooses the bottle.

Protein work separates a mixture, then asks which protein is which. Extraction and purification take the protein out of the cell. A marker shows the masses. A Western blot moves the separated proteins onto a membrane and probes them with an antibody. The membrane, nitrocellulose or PVDF, has to bind the protein and survive the washes. Antibodies and methods are in PubMed. Reference material is at ATCC.

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