4-Bromoaniline - ≥99% , CAS No.106-40-1

CAS: 106-40-1 Cat. No.: B103946 Peso molecular: 172.03 Beilstein Registry Number: 742031 Número EC: 203-393-9
Disponible para pedir
GRADE & PURITY ≥99%
Synonyms
4-Bromanilinu [Czech] | NSC7085 | NSC-7085 | P-BROMOANILINE | p-bromo-aniline | Q412773 | EINECS 203-393-9 | SMR001252237 | AM10670 | 0RR61TC330 | NCGC00260008-01 | AI3-17277 | NCGC00256346-01 | DTXCID301867 | Tox21_302910 | AC-13468 | Aniline, p-bromo |
Storage
Room temperature,Argon charged
Shipped In
FedEx DG Service
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
B103946-5g
10
9,90US$
25g
B103946-25g
6
17,90US$
100g
B103946-100g
3
31,90US$
250g
B103946-250g
1
59,90US$
500g
B103946-500g
1
104,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Argon charged Ships FedEx DG Service Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 30 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

4-Bromoaniline can be used as a starting material for the preparation of:
Sharpless asymmetric ligands for dihydroxylation of alkenes.
Chemical intermediates such as 4-bromophenyl azide , 4-bromonitrosobenzene , N-(4-bromophenyl)-4-methylbenzenesulfonamide , and ethyl 4-(4-(4-methylphenylsulfonamido)phenyl)butanoate.
It is also used in the surface functionalization of carbon nanotubes via preparation of 4-bromo benzenediazonium derivatives.

Specifications

Sinónimos
4-Bromanilinu [Czech] | NSC7085 | NSC-7085 | P-BROMOANILINE | p-bromo-aniline | Q412773 | EINECS 203-393-9 | SMR001252237 | AM10670 | 0RR61TC330 | NCGC00260008-01 | AI3-17277 | NCGC00256346-01 | DTXCID301867 | Tox21_302910 | AC-13468 | Aniline, p-bromo |
Especificaciones y pureza
≥99%
Mecanismos bioquímicos y fisiológicos
4-Bromoaniline reduces gluconeogenesis in renal cortical slices obtained from the kidneys of untreated, male Fischer 344 rats.
Condiciones de almacenamiento de almacenamiento
Room temperature, Argon charged
Enviado en
FedEx DG Service
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥99%
Nombres e identificadores
Pubchem Sid488180571
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488180571
Sonrisas canónicasC1=CC(=CC=C1N)Br
IUPAC Name4-bromoaniline
InChIKeyWDFQBORIUYODSI-UHFFFAOYSA-N
INCHI1S/C6H6BrN/c7-5-1-3-6(8)4-2-5/h1-4H,8H2
Isómeros SMILES C1=CC(=CC=C1N)Br
WGK Alemania 3
RTECS BW9280000
Número ONU 2811
Grupo de embalaje I
Peso molecular 172.03
Beilstein 742031
Reaxy-Rn 742031
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=742031&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClaseBenzene and substituted derivatives
SubclassAniline and substituted anilines
Intermediate Tree Nodes Not available
Direct ParentAniline and substituted anilines
Alternative Parents Bromobenzenes  Aryl bromides  Primary amines  Organopnictogen compounds  Organobromides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Aniline or substituted anilines - Halobenzene - Bromobenzene - Aryl halide - Aryl bromide - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Organobromide - Organohalogen compound - Amine - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as aniline and substituted anilines. These are organic compounds containing an aminobenzene moiety.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTH1R Tclin Parathyroid hormone receptor (47172 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1B1 Tchem Cytochrome P450 1B1 (1148 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALB Tchem Serum albumin (2651 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A1 Tchem Cytochrome P450 1A1 (1169 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLI Tchem DNA polymerase iota (116820 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Mapk1 MAP kinase ERK2 (650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

34 results found

Lot NumberCertificate TypeFechaArticulo
L2207207Certificate of AnalysisJun 09, 2026 B103946
L2207209Certificate of AnalysisJun 09, 2026 B103946
L2207464Certificate of AnalysisJun 09, 2026 B103946
C2429067Certificate of AnalysisJan 19, 2026 B103946
A2608114Certificate of AnalysisJan 17, 2026 B103946
B2624324Certificate of AnalysisJan 17, 2026 B103946
J2530133Certificate of AnalysisNov 03, 2025 B103946
B2225551Certificate of AnalysisSep 09, 2025 B103946
B2225501Certificate of AnalysisSep 09, 2025 B103946
B2225500Certificate of AnalysisSep 09, 2025 B103946
L2314016Certificate of AnalysisSep 09, 2025 B103946
G2502319Certificate of AnalysisJul 14, 2025 B103946
E2520127Certificate of AnalysisMay 24, 2025 B103946
B2512059Certificate of AnalysisFeb 19, 2025 B103946
I2412066Certificate of AnalysisSep 21, 2024 B103946
L2207198Certificate of AnalysisSep 20, 2024 B103946
L2207388Certificate of AnalysisSep 20, 2024 B103946
L2207210Certificate of AnalysisSep 20, 2024 B103946
L2207465Certificate of AnalysisSep 20, 2024 B103946
J2215136Certificate of AnalysisJul 18, 2024 B103946
B2225574Certificate of AnalysisDec 22, 2023 B103946
B2225558Certificate of AnalysisDec 22, 2023 B103946
H2109287Certificate of AnalysisMay 10, 2023 B103946
H2109286Certificate of AnalysisMay 10, 2023 B103946
H2109313Certificate of AnalysisMay 10, 2023 B103946
E2112146Certificate of AnalysisFeb 10, 2023 B103946
A2309396Certificate of AnalysisJan 16, 2023 B103946
A2309395Certificate of AnalysisJan 13, 2023 B103946
L2207206Certificate of AnalysisNov 24, 2022 B103946
L2207208Certificate of AnalysisNov 24, 2022 B103946
C2414022Certificate of AnalysisNov 24, 2022 B103946
A2507191Certificate of AnalysisNov 24, 2022 B103946
J2215140Certificate of AnalysisOct 21, 2022 B103946
E2015105Certificate of AnalysisApr 13, 2022 B103946

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Propiedades químicas y físicas
SolubilidadSoluble in alcohol and ether. Insoluble in cold water.
SensibilidadAir & Light sensitive.
Punto de ebullición (°C)124°C
Punto de fusión (°C)56-62°C
Peso molecular172.020 g/mol
XLogP32.300
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass170.968 Da
Monoisotopic Mass170.968 Da
Topological Polar Surface Area26.000 Ų
Heavy Atom Count8
Formal Charge0
Complexity66.900
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
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13. Da Xu, Yanwei Gao, Yang Sun, Zhaoyang Wang, Zhenhua Jiang, Xiangyu Jiang, Haibo Zhang.  (2019)  A Novel Graphene Nanoplatelets (GNPs) Dispersant: Polyaryletherketones with Pendent Pyrene Groups.  MACROMOLECULAR CHEMISTRY AND PHYSICS,  220  (9): (1800553).  [PMID:] [10.1002/macp.201800553]
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