1,1,2,2-Tetrabromoethane - purum p.a., ≥98%(GC), for separation (of mineral compounds) , CAS No.79-27-6

CAS: 79-27-6 Cat. No.: T475707 Peso molecular: 345.65 Beilstein Registry Number: 1098321 Número EC: 201-191-5 PubChem CID: 6588

GRADE & PURITY purum p.a., ≥98%(GC), for separation (of mineral compounds)

Synonyms

1,1,2,2-Tetrabromoethane, 98.0% | DTXSID1026083 | Tetrabromoacetylene | 1,1,2,2-Tetrabromoethylene | F1905-7026 | NCGC00257918-01 | 1,1,2,2-Tetrabroomethaan | Muthmanns liquid | Muthmann's liquid | LS-12933 | NCGC00091236-01 | WLN: EYEYEE | J-503707 | UNI

Storage

Room temperature

Shipped In

FedEx DG Service

Descripción general

Description

1,1,2,2-Tetrabromoethane (TBA) is a heavy liquid used for the density separation of minerals. The mixture of TBA, toluene, and tetrachloroethylene can be used for gravity separation.

Specifications

Sinónimos

1, 1, 2, 2-Tetrabromoethane, 98.0% | DTXSID1026083 | Tetrabromoacetylene | 1, 1, 2, 2-Tetrabromoethylene | F1905-7026 | NCGC00257918-01 | 1, 1, 2, 2-Tetrabroomethaan | Muthmanns liquid | Muthmann's liquid | LS-12933 | NCGC00091236-01 | WLN: EYEYEE | J-503707 | UNI

Especificaciones y pureza

purum p.a., ≥98%(GC), for separation (of mineral compounds)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

FedEx DG Service

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Grado

purum p.a.

Pureza

≥98%(GC)

Nombres e identificadores

• Sonrisas canónicas: C(C(Br)Br)(Br)Br
• IUPAC Name: 1,1,2,2-tetrabromoethane
• InChIKey: QXSZNDIIPUOQMB-UHFFFAOYSA-N
• INCHI: 1S/C2H2Br4/c3-1(4)2(5)6/h1-2H
• Isómeros SMILES: C(C(Br)Br)(Br)Br
• WGK Alemania: 2
• RTECS: KI8225000
• PubChem CID: 6588
• Número ONU: 2504
• Grupo de embalaje: III
• Peso molecular: 345.65
• Beilstein: 1098321
• Reaxy-Rn: 1098321

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organohalogen compounds
    • Clase Organobromides

• Kingdom: Organic compounds
• Superclass: Organohalogen compounds
• Clase: Organobromides
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Organobromides
• Alternative Parents: Hydrocarbon derivatives Alkyl bromides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Hydrocarbon derivative - Organobromide - Alkyl halide - Alkyl bromide - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as organobromides. These are compounds containing a chemical bond between a carbon atom and a bromine 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

Mecanismos de acción

Propiedades químicas y físicas

• Índice de refracción: 1.638
• Punto de ebullición (°C): 243.5°C
• Punto de fusión (°C): 0°C(lit.)
• Peso molecular: 345.650 g/mol
• XLogP3: 3.600
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 1
• Exact Mass: 345.685 Da
• Monoisotopic Mass: 341.689 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 26.500
• 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. Huaxun Luo, Weida Chen, Jiaming Hu, Feng Zhang, Xingbang Hu.  (2023)  Highly Selective Oxidation of Toluene to Benzaldehyde in Alkaline Systems.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.3c01049]

2. Chen Lu, Jiaming Hu, Yuning Meng, Aidong Zhou, Feng Zhang, Zhibing Zhang.  (2018)  The synergistic effect of benzyl benzoate on the selective oxidation of toluene to benzaldehyde.  CHEMICAL ENGINEERING RESEARCH & DESIGN,      [PMID:] [10.1016/j.cherd.2018.10.019]

3. Siyang Tang, Zhen Liu, Xiaowei Yan, Ning Li, Ruihua Cheng, Xuelian He, Boping Liu.  (2014)  Kinetic studies on the pyrrole–Cr-based Chevron-Phillips ethylene trimerization catalyst system.  APPLIED CATALYSIS A-GENERAL,      [PMID:] [10.1016/j.apcata.2014.04.006]

4. Feifan Yin, Murilege Chao, Jinhua Chen, Yanheng Yao, Miao He, Qiufeng Wang, Wenting Cheng, Yongliang Cai, Zhongyun Wang, Yang Xiang.  (2025)  One-Pot and Enzyme-Free Analysis of mRNA Vaccines Based on a Double Amplification System Featured by Adjustable Structure MNAzyme.  ANALYTICAL CHEMISTRY,      [PMID:40974015] [10.1021/acs.analchem.5c04634]