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4-Bromobenzylamine - 96%, high purity , CAS No.3959-07-7

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4-Bromobenzylamine - 96%, high purity , CAS No.3959-07-7

1 Citations

COA

Grade & Purity:

≥96%

Cas Number: 3959-07-7
Molecular Weight: 186.05
EC Number: 223-559-4
MDL number: MFCD00047931
PubChem CID: 77571

In stock

Item Number

B136595

Grouped product items
SKU	Size	Availability	Price
B136595-1g	1g	3	$67.90
B136595-5g	5g	3	$303.90
B136595-25g	25g	3	$1,365.90
B136595-100g	100g	2	$4,917.90
B136595-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$22,126.90

View related series

Nitrogenous compounds (2445) Non heterocyclic block (8163)

Basic Description

Synonyms

AC-25942 | BP-10081 | DTXSID70192704 | Q27464641 | AE-562/43286501 | B4713 | S-21O | J-200169 | SCHEMBL112119 | 4-Bromobenzenemethanamine | NSC-172131 | ZZB9N2KNT7 | 4-Bromobenzylamine, 96% | PZH | DETMS | FT-0659695 | STL185672 | AM86931 | p-Bromobenzyla

Specifications & Purity

≥96%

Storage Temp

Store at 2-8°C,Argon charged

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Product Description

Product Introduction

4-Bromobenzylamine (BBA), also known as p-bromobenzylamine, is an aryl bromide. The selective formation of nitrile or imine from BBA in the presence of red copper has been reported. The formal [4+4] reaction of BBA to form 2,6,9-triazabicyclo[3.3.1]nonane derivatives has been investigated.

Product Usage

4-Bromobenzylamine (p-Bromobenzylamine) may be used to synthesize 7-[(p-bromobenzyl)ureido]-7,8-dihydro-α-bisabolene.
It may be used to synthesize the following 4-biphenylmethylamine derivatives:
• (4′-fluoro-4-biphenyl)methylamine
• (4′-methoxy-4-biphenyl)methylamine
• (2′-methoxy-4-biphenyl)methylamine
• (3′-cyano-4-biphenyl)methylamine

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Benzene and substituted derivatives
    - Subclass Phenylmethylamines

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Benzene and substituted derivatives
Subclass	Phenylmethylamines
Intermediate Tree Nodes	Not available
Direct Parent	Phenylmethylamines
Alternative Parents	Benzylamines Bromobenzenes Aralkylamines Aryl bromides Organopnictogen compounds Organobromides Monoalkylamines Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Benzylamine - Phenylmethylamine - Aralkylamine - Bromobenzene - Halobenzene - Aryl bromide - Aryl halide - Amine - Organobromide - Organohalogen compound - Primary aliphatic amine - Organonitrogen compound - Primary amine - Hydrocarbon derivative - Organopnictogen compound - Organic nitrogen compound - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as phenylmethylamines. These are compounds containing a phenylmethtylamine moiety, which consists of a phenyl group substituted by an methanamine.
External Descriptors	Not available
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

Associated Targets(Human)

PNMT Tchem Phenylethanolamine N-methyltransferase (540 Activities)

Discover Target: PNMT

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	(4-bromophenyl)methanamine
INCHI	InChI=1S/C7H8BrN/c8-7-3-1-6(5-9)2-4-7/h1-4H,5,9H2
InChIKey	XRNVSPDQTPVECU-UHFFFAOYSA-N
Smiles	C1=CC(=CC=C1CN)Br
Isomeric SMILES	C1=CC(=CC=C1CN)Br
WGK Germany	3
Molecular Weight	186.05
Reaxy-Rn	2689604
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2689604&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.

13 results found

Lot Number	Certificate Type	Date	Item
F2424515	Certificate of Analysis	Jul 01, 2024	B136595
E2430077	Certificate of Analysis	Jan 05, 2024	B136595
C2218433	Certificate of Analysis	Jan 05, 2024	B136595
C2218432	Certificate of Analysis	Jan 05, 2024	B136595
C2218451	Certificate of Analysis	Jan 05, 2024	B136595
C2218442	Certificate of Analysis	Jan 05, 2024	B136595
H1507034	Certificate of Analysis	Mar 15, 2023	B136595
D2121131	Certificate of Analysis	Feb 09, 2023	B136595
D2121132	Certificate of Analysis	Feb 09, 2023	B136595
D2121133	Certificate of Analysis	Feb 09, 2023	B136595
E1921141	Certificate of Analysis	Jan 25, 2023	B136595
J2214268	Certificate of Analysis	Oct 22, 2022	B136595
F2019010	Certificate of Analysis	Apr 27, 2022	B136595

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Chemical and Physical Properties

Sensitivity	air & Heat &light sensitive
Flash Point(°F)	>230 °F
Flash Point(°C)	>110 °C
Boil Point(°C)	125 °C
Melt Point(°C)	26 °C
Molecular Weight	186.050 g/mol
XLogP3	1.900
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	1
Exact Mass	184.984 Da
Monoisotopic Mass	184.984 Da
Topological Polar Surface Area	26.000 Å²
Heavy Atom Count	9
Formal Charge	0
Complexity	77.000
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

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Zhizhu Yue, Yonghe Yu, Tianjun Hu, Ying Wang, Lulu Cao, Yanxia Zhang, Yuhong Chang, Linjuan Pei, Jianfeng Jia. (2024) One-step solvothermal formation of Cu - Doped Cu2WO4(OH)2 nanocatalysts for efficient photocatalytic amine oxidation coupling. Materials Today Chemistry, 36 (101932).

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