4-Nitroaniline - AR, ≥99% , CAS No.100-01-6

CAS: 100-01-6 Cat. No.: N111641 Fórmula: C6H6N2O2 Peso molecular: 138.12 Beilstein Registry Number: 508690 Número CE: 202-810-1
Disponível para encomenda
GRAU & PUREZA AR ? Analytical Reagent grade — high-purity chemicals meeting strict assay limits for lab analysis. Use when accuracy matters and trace impurities could skew results. ≥99%
Synonyms
DTXSID8020961 | InChI=1/C6H6N2O2/c7-5-1-3-6(4-2-5)8(9)10/h1-4H,7H | NCGC00091426-02 | 4-Nitroaniline, >=99% | Fast Red GG Salt | MFCD00007858 | Nitrazol CF extra | p-Nitroaniline | Fast Red Salt 2J | Red 2G Base | SMR001372024 | 4-Nitroaniline, 99% | CHEB
Storage
Room temperature
Shipped In
FedEx DG Service
★
Tamanho
Alemanha (EU)
USA*
Preço
Qtd
100g
N111641-100g
—
1 Em stock
12,93€
500g
N111641-500g
—
2 Em stock
46,77€
Enter a quantity for the sizes you want to add.
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Por que este grau

AR, ≥99% AR para fluxos de trabalho cromatográficos e analíticos sensíveis que exigem interferência mínima da linha de base.

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Armazenamento e envio

Room temperature Envio FedEx DG Service. Consulte o COA específico do lote para obter as especificações exatas.

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Documentos de qualidade

SDS, COA, ficha técnica e folha de especificações disponíveis para download. COA específico do lote acessível por meio de pesquisa por número de lote.

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Comprovação documental

Citado em 152 publicações revisadas por pares nas áreas de cromatografia, síntese orgânica e reações de acoplamento cruzado.

Visão geral

A common chromophore and potentially useful syntetic reagent.

Especificações

Sinónimos
DTXSID8020961 | InChI=1/C6H6N2O2/c7-5-1-3-6(4-2-5)8(9)10/h1-4H,7H | NCGC00091426-02 | 4-Nitroaniline, >=99% | Fast Red GG Salt | MFCD00007858 | Nitrazol CF extra | p-Nitroaniline | Fast Red Salt 2J | Red 2G Base | SMR001372024 | 4-Nitroaniline, 99% | CHEB
Especificações e pureza
AR, ≥99%
Mecanismos bioquímicos e fisiológicos
4-Nitroaniline forms molecular adducts with 4-amino benzoic acid. It reacts with nitrite ion in hydrochloric acid medium to form 4-nitrophenyldiazonium chloride, which couples with naphth-1-ol in alkaline medium to give a purple azo dye. Photocatalytic de
Condições de armazenamento de armazenamento
Room temperature
Enviado em
FedEx DG Service
Grau
AR
Pureza
≥99%
Nomes e identificadores
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508813299
Sorrisos canónicos
C1=CC(=CC=C1N)[N+](=O)[O-]
IUPAC Name
4-nitroaniline
InChIKey
TYMLOMAKGOJONV-UHFFFAOYSA-N
INCHI
1S/C6H6N2O2/c7-5-1-3-6(4-2-5)8(9)10/h1-4H,7H2
SMILES isoméricas
C1=CC(=CC=C1N)[N+](=O)[O-]
WGK Alemanha
2
RTECS
BY7000000
Número UN
1661
Grupo de embalagem
II
Peso molecular
138.12
Beilstein
508690
Reaxy-Rn
508690
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=508690&ln=

Documentação

📋 Ficha de dados de segurança (FDS)

Documento abrangente sobre perigos, manuseamento, armazenamento e conformidade regulamentar.

<<<<<<< HEAD Baixar SDS → ======= Baixar SDS → >>>>>>> release248-p3

✅ Certificado de análise (COA)

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📊 Ficha técnica

Resumo de referência rápida das especificações e aplicações do produto.

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🔬 Folha de especificações

Atributos de qualidade completos e critérios de aceitação para este grau.

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Dados avançados

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClasseBenzene and substituted derivatives
SubclassNitrobenzenes
Intermediate Tree Nodes Not available
Direct ParentNitrobenzenes
Alternative Parents Nitroaromatic compounds  Aniline and substituted anilines  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Primary amines  Organopnictogen compounds  Organic zwitterions  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Nitrobenzene - Nitroaromatic compound - Aniline or substituted anilines - C-nitro compound - Organic nitro compound - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic nitrogen compound - Organic zwitterion - Primary amine - Organonitrogen compound - Amine - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Aromatic homomonocyclic compound
DescriçãoThis compound belongs to the class of organic compounds known as nitrobenzenes. These are compounds containing a nitrobenzene moiety, which consists of a benzene ring with a carbon bearing a nitro group.
External Descriptors a small molecule
Estrutura 3D
Modelo de Estrutura Química Interativa





Alvos associados (humanos)
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1B1 Tchem Cytochrome P450 1B1 (1148 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
GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Lymphoblastoid cell (5959 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BAZ2B Tchem Bromodomain adjacent to zinc finger domain protein 2B (56204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ATXN2 Tbio Ataxin-2 (54410 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Alvos associados (não humanos)
PREP Prolyl endopeptidase (14 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GCN5 Histone acetyltransferase GCN5 (89 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Colon (26 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TGR Thioredoxin glutathione reductase (28579 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de ação
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
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.

25 results found

Lot NumberCertificate TypeDataItem
I2622632I2622632Certificate of AnalysisSep 12, 2026 N111641
I2622634I2622634Certificate of AnalysisSep 12, 2026 N111641
I2622633I2622633Certificate of AnalysisSep 12, 2026 N111641
C2521876C2521876Certificate of AnalysisFeb 13, 2025 N111641
D2620031D2620031Certificate of AnalysisFeb 13, 2025 N111641
C2510252C2510252Certificate of AnalysisFeb 13, 2025 N111641
C2510250C2510250Certificate of AnalysisFeb 13, 2025 N111641
G2402377G2402377Certificate of AnalysisApr 24, 2024 N111641
G2402378G2402378Certificate of AnalysisApr 24, 2024 N111641
J2414399J2414399Certificate of AnalysisAug 30, 2023 N111641
A2507204A2507204Certificate of AnalysisAug 30, 2023 N111641
F2604119F2604119Certificate of AnalysisAug 30, 2023 N111641
F2604120F2604120Certificate of AnalysisAug 30, 2023 N111641
I2328483I2328483Certificate of AnalysisAug 30, 2023 N111641
I2328484I2328484Certificate of AnalysisAug 30, 2023 N111641
I2328485I2328485Certificate of AnalysisAug 30, 2023 N111641
K2211742K2211742Certificate of AnalysisOct 13, 2022 N111641
K2211388K2211388Certificate of AnalysisOct 13, 2022 N111641
K2211389K2211389Certificate of AnalysisOct 13, 2022 N111641
B2318881B2318881Certificate of AnalysisOct 12, 2022 N111641
B2318876B2318876Certificate of AnalysisOct 12, 2022 N111641
B2318854B2318854Certificate of AnalysisOct 12, 2022 N111641
A2220215A2220215Certificate of AnalysisDec 13, 2021 N111641
A2220210A2220210Certificate of AnalysisDec 13, 2021 N111641
A2220208A2220208Certificate of AnalysisDec 13, 2021 N111641
Propriedades químicas e físicas
SolubilidadeSoluble in hot water and alcohol.
SensibilidadeMoisture sensitive.
Ponto de inflamação (°C)199 °C
Ponto de ebulição (°C)332 °C
Ponto de fusão (°C)146°C
Peso molecular138.120 g/mol
XLogP31.400
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count0
Exact Mass138.043 Da
Monoisotopic Mass138.043 Da
Topological Polar Surface Area71.800 Ų
Heavy Atom Count10
Formal Charge0
Complexity124.000
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
FAQs e artigos
Citations of This Product
Calculadoras de soluções
Revisões

Avaliações dos Clientes

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