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Bromobenzene - Standard for GC,>99.5%(GC), high purity , CAS No.108-86-1

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Item Number
B103390
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B103390-5ml
5ml
5
$25.90

Basic Description

Synonyms BROMOBENZENE [HSDB] | EINECS 203-623-8 | HSDB 47 | NCGC00091842-03 | PhBr | B0439 | Bromobenzene, >=99.5% (GC) | Monobromobenzene | BROMOBENZENE [MI] | DTXSID5024637 | A801934 | AI3-09059 | CO4D5J547L | J-519941 | Tox21_200849 | MLS000515541 | C6H5Br | Be
Specifications & Purity Standard for GC, ≥99.5%(GC)
Storage Temp Protected from light,Room temperature
Shipped In Normal
Grade Standard for GC

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Halobenzenes
Intermediate Tree Nodes Not available
Direct Parent Bromobenzenes
Alternative Parents Aryl bromides  Organobromides  Hydrocarbon derivatives  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Bromobenzene - Aryl halide - Aryl bromide - Hydrocarbon derivative - Organobromide - Organohalogen compound - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as bromobenzenes. These are organic compounds containing a bromine atom attached to a benzene ring.
External Descriptors a bromoaromatic compound

Associated Targets(Human)

PDE5A Tclin Phosphodiesterase 5A (5113 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HMGCR Tclin HMG-CoA reductase (2475 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
INSR Tclin Insulin receptor (5558 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PGR Tclin Progesterone receptor (8562 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
VDR Tclin Vitamin D receptor (26531 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ACE Tclin Angiotensin-converting enzyme (1423 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD2 Tclin Dopamine D2 receptor (23596 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD4 Tchem Dopamine D4 receptor (7907 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HRH2 Tclin Histamine H2 receptor (5428 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CALCR Tclin Calcitonin receptor (2215 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC6A4 Tclin Serotonin transporter (12625 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HRH1 Tclin Histamine H1 receptor (7573 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
OPRM1 Tclin Mu opioid receptor (19785 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD3 Tclin Dopamine D3 receptor (14368 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
OPRD1 Tclin Delta opioid receptor (15096 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
OPRK1 Tclin Kappa opioid receptor (16155 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR4 Tclin Serotonin 4 (5-HT4) receptor (2068 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ESR2 Tclin Estrogen receptor beta (9272 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYSLTR1 Tclin Cysteinyl leukotriene receptor 1 (2118 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ERBB2 Tclin Receptor protein-tyrosine kinase erbB-2 (7851 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CHRM4 Tclin Muscarinic acetylcholine receptor M4 (6041 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CHRM5 Tclin Muscarinic acetylcholine receptor M5 (4677 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mc4r Melanocortin receptor 4 (1205 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Ltc4s Leukotriene C4 synthase (1 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Sigmar1 Sigma opioid receptor (160 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Npy1r Neuropeptide Y receptor type 1 (8 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Cckar Cholecystokinin A receptor (90 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nos2 Nitric oxide synthase, inducible (3573 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mmp9 Matrix metalloproteinase 9 (38 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name bromobenzene
INCHI InChI=1S/C6H5Br/c7-6-4-2-1-3-5-6/h1-5H
InChIKey QARVLSVVCXYDNA-UHFFFAOYSA-N
Smiles C1=CC=C(C=C1)Br
Isomeric SMILES C1=CC=C(C=C1)Br
WGK Germany 2
UN Number 2514
Packing Group III
Molecular Weight 157.01
Beilstein 1236661
Reaxy-Rn 1236661
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1236661&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot Number Certificate Type Date Item
A2506380 Certificate of Analysis Jan 09, 2025 B103390
J2312014 Certificate of Analysis Oct 20, 2023 B103390
D1926069 Certificate of Analysis Nov 10, 2022 B103390
J2210052 Certificate of Analysis Oct 12, 2022 B103390
C2222050 Certificate of Analysis Mar 25, 2022 B103390

Chemical and Physical Properties

Solubility Insoluble in water, soluble in most organic solvents such as methanol, ether, acetone, benzene, and carbon tetrachloride.
Sensitivity Light sensitive.
Refractive Index 1.5602
Flash Point(°F) 123.8 °F - closed cup
Flash Point(°C) 51℃
Boil Point(°C) 156.2°C
Melt Point(°C) -30.6°C
Molecular Weight 157.010 g/mol
XLogP3 3.000
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 0
Rotatable Bond Count 0
Exact Mass 155.957 Da
Monoisotopic Mass 155.957 Da
Topological Polar Surface Area 0.000 Ų
Heavy Atom Count 7
Formal Charge 0
Complexity 46.100
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

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3. Xulong Pang, Yong Li, Xiaofu Wu, Bingmiao Zhang, Ming Hao, Yan Zhu, Yi Zhang, Chuanjiang Qin, Hongmei Zhan, Chuanli Qin.  (2023)  Phosphate ester functionalized fluorene-benzothiadiazole alternating copolymer/hydroxylated g-C3N4 heterojunctions for efficient hydrogen evolution under visible-light irradiation.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,  652  (1405). 
4. Fan Wu, Hao Li, Yang Pan, Yingjia Wang, Yonghui Sun, Jianming Pan.  (2023)  Sustainable utilization of palladium from industrial catalytic waste by a smart magnetic nano stirring robot.  SEPARATION AND PURIFICATION TECHNOLOGY,  315  (123536). 
5. Hao Ling, Lei Wang, Qixuan Lin, Quanbo Huang, Xiaoqian Zhang, Junli Ren, Ning Li, Cheng Zhou, Zhiwei Lin, Jingpeng Zhou, Wenguang Wei, Xiaohui Wang.  (2023)  Antimicrobial cellulose paper tuned with chitosan fibers for high-flux oil/water separation.  CARBOHYDRATE POLYMERS,  312  (120794). 
6. Qiuyu Lin, Luyun Xue, Jiannan Sun, Yuanchao Wang, Heyong Cheng.  (2022)  Suzuki C–C Coupling in Paper Spray Ionization: Microsynthesis of Biaryls and High-Sensitivity MS Detection of Aryl Bromides.  JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY,  33  (10): (1921–1935). 
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8. Yaoxia Li, Zehang Cui, Guoqiang Li, Haoyu Bai, Ruyuan Dai, Yingzi Zhou, Yan Jiao, Yuegan Song, Yi Yang, Senyun Liu, Moyuan Cao.  (2022)  Directional and Adaptive Oil Self-Transport on a Multi-Bioinspired Grooved Conical Spine.  ADVANCED FUNCTIONAL MATERIALS,  32  (27): (2201035). 
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11. Danning Gao, Qi Zhang, Zhifeng Liu, Fureng Zhang, Faliang Gou, Guiying Xing, Shujing Zhou, Linjun Shao, Jinjing Li, Yijun Du, Chenze Qi.  (2021)  Stabilization of palladium nanoparticles inside chitosan derived N-doped carbon nanofibers for Heck reaction.  JOURNAL OF APPLIED POLYMER SCIENCE,  139  (10): (51742). 
12. Shangjie Jiang, Shisheng Zhou.  (2021)  A method for preparing the pH-responsive superhydrophobic paper with high stability.  Materials Research Express,  (6): (65306). 
13. Yuan Li, Biao Pei, Junjie Chen, Shaosuo Bing, Linxiao Hou, Qi Sun, Gang Xu, Zhikan Yao, Lin Zhang.  (2021)  Hollow nanosphere construction of covalent organic frameworks for catalysis: (Pd/C)@TpPa COFs in Suzuki coupling reaction.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,  591  (273). 
14. Dandan Lu, Keyang Yin, Ya Zhao, Zelin Gao, Nicolas Godbert, Hongmei Li, Hongguang Li, Jingcheng Hao.  (2021)  Facile synthesis of alkylated carbon dots with blue emission in halogenated benzene solvents.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,  613  (126129). 
15. Zhong Shaofeng.  (2020)  Preparation of chitosan/poly(methacrylic acid) supported palladium nanofibers as an efficient and stable catalyst for Heck reaction.  JOURNAL OF CHEMICAL SCIENCES,  132  (1): (1-9). 
16. Benben Zhang, Zeyu Ye, Min Qin, Qingqing Wang, Yijun Du, Chenze Qi, Linjun Shao.  (2020)  Palladium complex embedded crosslinked polystyrene nanofibers as a green and efficient heterogeneous catalyst for coupling reactions.  JOURNAL OF APPLIED POLYMER SCIENCE,  138  (2): (49666). 
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22. Li Jiali, Kong Xianggui, Jiang Meihong, Lei Xiaodong.  (2018)  Uniformly dispersed Pd nanoparticles anchored Co(OH)2/Cu(OH)2 hierarchical nanotube array as high active structured catalyst for Suzuki–Miyaura coupling reactions.  JOURNAL OF MATERIALS SCIENCE,  53  (24): (16263-16275). 
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24. Kaitao Zhang, Minggui Shen, He Liu, Shibin Shang, Dan Wang, Henrikki Liimatainen.  (2018)  Facile synthesis of palladium and gold nanoparticles by using dialdehyde nanocellulose as template and reducing agent.  CARBOHYDRATE POLYMERS,  186  (132). 
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