BIS-TRIS hydrochloride - ≥99% , CAS No.124763-51-5

CAS: 124763-51-5 Cat. No.: B120627 Peso molecular: 245.7 Número EC: 695-696-1

GRADE & PURITY ≥99%

Synonyms

E75773 | 1,3-Propanediol, 2-[bis(2-hydroxyethyl)amino]-2-(hydroxymethyl)-, hydrochloride (1:1) | BIS-TRIS hydrochloride, Vetec(TM) reagent grade, 99% | 1,3-Propanediol, 2-(bis(2-hydroxyethyl)amino)-2-(hydroxymethyl)-, hydrochloride (1:1) | 2,2-Bis(hydroxy

Storage

Protected from light,Room temperature,Argon charged

Shipped In

Normal

Descripción general

useful pH range 5.8 - 7.2 pKa 6.5

Specifications

Sinónimos

E75773 | 1, 3-Propanediol, 2-[bis(2-hydroxyethyl)amino]-2-(hydroxymethyl)-, hydrochloride (1:1) | BIS-TRIS hydrochloride, Vetec(TM) reagent grade, 99% | 1, 3-Propanediol, 2-(bis(2-hydroxyethyl)amino)-2-(hydroxymethyl)-, hydrochloride (1:1) | 2, 2-Bis(hydroxy

Especificaciones y pureza

≥99%

Condiciones de almacenamiento de almacenamiento

Protected from light, Room temperature, Argon charged

Enviado en

Normal

Pureza

≥99%

Nombres e identificadores

• Pubchem Sid: 488199332
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488199332
• Sonrisas canónicas: C(CO)N(CCO)C(CO)(CO)CO.Cl
• IUPAC Name: 2-[bis(2-hydroxyethyl)amino]-2-(hydroxymethyl)propane-1,3-diol;hydrochloride
• InChIKey: VEYRVLHAMHQVTC-UHFFFAOYSA-N
• INCHI: 1S/C8H19NO5.ClH/c10-3-1-9(2-4-11)8(5-12,6-13)7-14;/h10-14H,1-7H2;1H
• Isómeros SMILES: C(CO)N(CCO)C(CO)(CO)CO.Cl
• WGK Alemania: 3
• Peso molecular: 245.7
• Reaxy-Rn: 15588459
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=15588459&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Alkanolamines
• Direct Parent: 1,2-aminoalcohols
• Alternative Parents: Trialkylamines Primary alcohols Organopnictogen compounds Hydrochlorides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tertiary aliphatic amine - Tertiary amine - 1,2-aminoalcohol - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic acyclic compound
• Descripción: 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: 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

Propiedades químicas y físicas

• Sensibilidad: light & Moisture sensitive
• Peso molecular: 245.700 g/mol
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 8
• Exact Mass: 245.103 Da
• Monoisotopic Mass: 245.103 Da
• Topological Polar Surface Area: 104.000 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 125.000
• 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: 2

XLogP3

Referencias

1. Yizhou Wu, Jesse Ward-Bond, Donglin Li, Shaohua Zhang, Jiafu Shi, Zhongyi Jiang.  (2018)  g-C3N4@α-Fe2O3/C Photocatalysts: Synergistically Intensified Charge Generation and Charge Transfer for NADH Regeneration.  ACS Catalysis,      [PMID:] [10.1021/acscatal.8b00070]

2. Fei Fan, Chao Cai, Lei Gao, Jun Li, Ping Zhang, Guoyun Li, Chunxia Li, Guangli Yu.  (2017)  Microwave-assisted synthesis of glycopolymers by ring-opening metathesis polymerization (ROMP) in an emulsion system.  Polymer Chemistry,  8  (44): (6709-6719).  [PMID:] [10.1039/C7PY01415E]