BIS-TRIS propane - UltraBio™, Ultra pure, ≥99%(T) , CAS No.64431-96-5

CAS: 64431-96-5 Cat. No.: B433230 Peso molecular: 282.33 Beilstein Registry Number: 1786109 Número EC: 264-899-3

GRADE & PURITY UltraBio™, Ultra pure, ≥99%(T)

Synonyms

Bis-Tris propane | MFCD00004689 | Q4917173 | SY018877 | 2-[3-(2-HYDROXY-1,1-DIHYDROXYMETHYL-ETHYLAMINO)-PROPYLAMINO]-2-HYDROXYMETHYL-PROPANE-1,3-DIOL | BIS-TRIS propane, anhydrous, free-flowing, Redi-Dri(TM), >=99.0% | UNII-N5YD0CS4DO | 1,3-Bis(tris[hydro

Storage

Room temperature

Shipped In

Normal

Descripción general

Other Notes

Easily compare specifications for BIS-TRIS propane products with the BIS-TRIS propane specification table .

Specifications

Sinónimos

Bis-Tris propane | MFCD00004689 | Q4917173 | SY018877 | 2-[3-(2-HYDROXY-1, 1-DIHYDROXYMETHYL-ETHYLAMINO)-PROPYLAMINO]-2-HYDROXYMETHYL-PROPANE-1, 3-DIOL | BIS-TRIS propane, anhydrous, free-flowing, Redi-Dri(TM), >=99.0% | UNII-N5YD0CS4DO | 1, 3-Bis(tris[hydro

Especificaciones y pureza

UltraBio™, Ultra pure, ≥99%(T)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Grado

Ultra pure, UltraBio™

Pureza

≥99%(T)

Nombres e identificadores

• Sonrisas canónicas: C(CNC(CO)(CO)CO)CNC(CO)(CO)CO
• IUPAC Name: 2-[3-[[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]amino]propylamino]-2-(hydroxymethyl)propane-1,3-diol
• InChIKey: HHKZCCWKTZRCCL-UHFFFAOYSA-N
• INCHI: 1S/C11H26N2O6/c14-4-10(5-15,6-16)12-2-1-3-13-11(7-17,8-18)9-19/h12-19H,1-9H2
• Isómeros SMILES: C(CNC(CO)(CO)CO)CNC(CO)(CO)CO
• WGK Alemania: 3
• Peso molecular: 282.33
• Beilstein: 1786109
• Reaxy-Rn: 1786109
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1786109&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: Dialkylamines Primary alcohols Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: 1,2-aminoalcohol - Secondary amine - Secondary aliphatic amine - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - 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: hexol

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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: H2O: 1M, clear, colorless
• Punto de fusión (°C): 164-165°C
• Peso molecular: 282.330 g/mol
• XLogP3: -4.600
• Hydrogen Bond Donor Count: 8
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 12
• Exact Mass: 282.179 Da
• Monoisotopic Mass: 282.179 Da
• Topological Polar Surface Area: 145.000 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 183.000
• 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: 1

Referencias

1. Jie Gu, Shuyun Zheng, Xiaolong Lu, Hao Zhang, Kai Ren, Ziqiang Liu, Chao Liu, Chunrui Wu.  (2024)  A new strategy for solving hydrophobic membrane wetting: membrane structure design for membrane pore drying by spontaneous dehydration.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2024.123664]

2. Jiandong Shen, Bijiang Zhong, Wenshui Xia, Yanshun Xu.  (2024)  Action of structural proteins in textural deterioration of grass carp (Ctenopharyngodon idellus) fillets during refrigerated storage.  INTERNATIONAL JOURNAL OF FOOD SCIENCE AND TECHNOLOGY,  59  (4): (2659-2666).  [PMID:] [10.1111/ijfs.17010]

3. Seokjoon Kim, Seungjin Lee, Seokhwan Kim, Jiye Shin, Byung Seok Cha, Eun Sung Lee, Ki Soo Park.  (2024)  Colorimetric detection of arsenite using Tris-mediated gold nanoparticle aggregation and chitosan lateral flow strip-based signal enhancement.  SENSORS AND ACTUATORS B-CHEMICAL,      [PMID:] [10.1016/j.snb.2024.135469]

4. Bao-Di Ma, Jia-Yi Li, Jian-He Xu, Tao Yu, Xu-Dong Kong.  (2025)  ADP-ribose is a competitive inhibitor of methanol dehydrogenases from Bacillus methanolicus.  JOURNAL OF BIOLOGICAL CHEMISTRY,      [PMID:40818608] [10.1016/j.jbc.2025.110599]

5. Yu Han, Yuelin Luo, Bao-Di Ma, Jie Li, Jian-He Xu, Xu-Dong Kong.  (2024)  Structural Insights of a cis-Epoxysuccinate Hydrolase Facilitate the Development of Robust Biocatalysts for the Production of l-(+)-Tartrate.  BIOCHEMISTRY,      [PMID:38803051] [10.1021/acs.biochem.4c00141]