BIS-TRIS(Bis-Tris) - synthetic , CAS No.6976-37-0

CAS: 6976-37-0 Cat. No.: B755922 Formula: C₈H₁₉NO₅ Peso molecolare: 209.24 Beilstein Registry Number: 2205275 Numero EC: 686-880-2

QUALITÀ & PUREZZA synthetic

Synonyms

2-[bis(2-hydroxyethyl)amino]-2-(hydroxymethyl)propane-1,3-diol | Bis(2-hydroxyethyl)aminotris(hydroxymethyl)methane | 2,2-Bis(hydroxymethyl)-2,2',2''-nitrilotriethanol

Storage

Protected from light,Room temperature,Argon charged

Shipped In

Normal

Panoramica

Bis Tris is used in a wide variety of biological applications including protein separation buffers, cell culture media, electrophoresis separations and diagnostic reagent formulations.

Specifiche

Sinonimi

2-[bis(2-hydroxyethyl)amino]-2-(hydroxymethyl)propane-1,3-diol | Bis(2-hydroxyethyl)aminotris(hydroxymethyl)methane | 2,2-Bis(hydroxymethyl)-2,2',2''-nitrilotriethanol

Specifiche e purezza

synthetic

Intervallo di PH utile

5.8-7.2

Condizioni di conservazione di stoccaggio

Protected from light,Room temperature,Argon charged

Spedito in

Normal

Nomi e identificatori

Sorrisi canonici

OCCN(CCO)C(CO)(CO)CO

IUPAC Name

2-[bis(2-hydroxyethyl)amino]-2-(hydroxymethyl)propane-1,3-diol

InChIKey

OWMVSZAMULFTJU-UHFFFAOYSA-N

INCHI

1S/C8H19NO5/c10-3-1-9(2-4-11)8(5-12,6-13)7-14/h10-14H,1-7H2

Isomeri SMILES

C(CO)N(CCO)C(CO)(CO)CO

WGK Germania

3

Peso molecolare

209.24

Beilstein

2205275

Reaxy-Rn

2205275

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2205275&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Classe Organonitrogen compounds
      • Subclass Amines
        • Level5 Alkanolamines
          • Level6 1,2-aminoalcohols

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Classe: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Alkanolamines
• Direct Parent: 1,2-aminoalcohols
• Alternative Parents: Trialkylamines Primary alcohols Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tertiary aliphatic amine - Tertiary amine - 1,2-aminoalcohol - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as 1,2-aminoalcohols. These are organic compounds containing an alkyl chain with an amine group bound to the C1 atom and an alcohol group bound to the C2 atom.
• External Descriptors: pentol

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

Proprietà chimiche e fisiche

• Solubilità: H 2 O: 0.1 M, clear, colorless
• Punto di fusione (°C): 103-104°C