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2-Bromopropane - reagent grade,98%, high purity , CAS No.75-26-3
Basic Description
Synonyms
NCGC00257910-01 | AKOS000119846 | InChI=1/C3H7Br/c1-3(2)4/h3H,1-2H | NCGC00091451-01 | STL146524 | 1-isopropylbromide | 2-Bromopropane [UN2344] [Flammable liquid] | 2-Bromopropane, purum, >=99.0% (GC) | Isopropylbromide | iso-propylbromide | 2-Bromopropa
Specifications & Purity
CP, ≥98%
Shipped In
Normal
Grade
CP
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organohalogen compounds
Class
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
Description
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.
Associated Targets(Human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
Pubchem Sid
488180056
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488180056
IUPAC Name
2-bromopropane
INCHI
InChI=1S/C3H7Br/c1-3(2)4/h3H,1-2H3
InChIKey
NAMYKGVDVNBCFQ-UHFFFAOYSA-N
Smiles
CC(C)Br
Isomeric SMILES
CC(C)Br
WGK Germany
1
RTECS
TX4111000
UN Number
2344
Molecular Weight
122.99
Beilstein
741852
Reaxy-Rn
741852
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=741852&ln=
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Solubility in water: Practically Insoluble; Degree of Solubility in water: 318 mg/l 20 °C; Miscible with Chloroform,Benzene,Ether,Alcohol
Refractive Index
1.4251
Flash Point(°F)
66.2 °F
Flash Point(°C)
19℃
Boil Point(°C)
59.38°C
Melt Point(°C)
-89°C
Molecular Weight
122.990 g/mol
XLogP3
1.800
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
0
Exact Mass
121.973 Da
Monoisotopic Mass
121.973 Da
Topological Polar Surface Area
0.000 Ų
Heavy Atom Count
4
Formal Charge
0
Complexity
10.800
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
Citations of This Product
1.
Zhong ZhenHua, Chen YuPing, Xia HongYing, Chen ZhenZhen, Cheng QiZhen.
(2021)
Development and Validation of a Sensitive GC–MS/MS Method for the Determination of Five Potential Genotoxic Impurities in Abiraterone Acetate.
JOURNAL OF CHROMATOGRAPHIC SCIENCE,
60
(2):
(105-110).
2.
Dan He, Ying Wu, Zhengping Liu, Tuo Zhao.
(2017)
The synthesis of poly(phenylene sulfide sulfone) in ionic liquids at atmospheric pressure.
RSC Advances,
7
(63):
(39604-39610).
3.
Li Yongqiang, Yang Siwei, Bao Wancheng, Tao Quan, Jiang Xiuyun, Li Jipeng, He Peng, Wang Gang, Qi Kai, Dong Hui, Ding Guqiao, Xie Xiaoming.
(2024)
Accelerated proton dissociation in an excited state induces superacidic microenvironments around graphene quantum dots.
Nature Communications,
15
(1):
(1-13).
4.
Ting Xu, Zihan Xue, Xinhui Li, Miaomiao Zhang, Ruige Yang, Shangshang Qin, Yong Guo.
(2025)
Development of Membrane-Targeting Osthole Derivatives Containing Pyridinium Quaternary Ammonium Moieties with Potent Anti-Methicillin-Resistant Staphylococcus aureus Properties.
JOURNAL OF MEDICINAL CHEMISTRY,
68
(7):
(7459-7475).
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