4-Hydroxy benzaldehyde - 10mM in DMSO , CAS No.123-08-0

CAS: 123-08-0 Cat. No.: H421000 Fórmula: C7H6O2 Peso molecular: 122.12 Beilstein Registry Number: 471352 Número CE: 204-599-1
Disponível para encomenda
GRAU & PUREZA 10mM in DMSO
Synonyms
1k03 | AC-2984 | CCRIS 8911 | p-Hydroxybenzaldehyde, Pract. | P-HYDROXYBENZALDEHYDE [MI] | 4-Formylphenol | 4-formyl-phenol | Benzaldehyde, p-hydroxy- | FT-0669408 | 4-Hydroxy-benzaldehyde-1,2,3,4,5,6-13C6 | AB-131/40191192 | FEMA NO. 3984 | 4-Hydroxybenz
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
★
Tamanho
Alemanha (EU)
USA*
Preço
Qtd
1ml
H421000-1ml
—
2 Em stock
25,08€
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Por que este grau

10mM in DMSO para fluxos de trabalho cromatográficos e analíticos sensíveis que exigem interferência mínima da linha de base.

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Armazenamento e envio

Store at -80°C Envio Dry ice packs + Cold packs. 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 238 publicações revisadas por pares nas áreas de cromatografia, síntese orgânica e reações de acoplamento cruzado.

Visão geral

application:

4-Hydroxybenzaldehyde is used as a chemical that maintains bactericidal activity when tested against certain bacteria strains.

Especificações

Sinónimos
1k03 | AC-2984 | CCRIS 8911 | p-Hydroxybenzaldehyde, Pract. | P-HYDROXYBENZALDEHYDE [MI] | 4-Formylphenol | 4-formyl-phenol | Benzaldehyde, p-hydroxy- | FT-0669408 | 4-Hydroxy-benzaldehyde-1,2,3,4,5,6-13C6 | AB-131/40191192 | FEMA NO. 3984 | 4-Hydroxybenz
Especificações e pureza
10mM in DMSO
Condições de armazenamento de armazenamento
Store at -80°C
Enviado em
Dry ice packs + Cold packs
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Nomes e identificadores
Pubchem Sid
Sorrisos canónicos
C1=CC(=CC=C1C=O)O
IUPAC Name
4-hydroxybenzaldehyde
InChIKey
RGHHSNMVTDWUBI-UHFFFAOYSA-N
INCHI
1S/C7H6O2/c8-5-6-1-3-7(9)4-2-6/h1-5,9H
SMILES isoméricas
C1=CC(=CC=C1C=O)O
WGK Alemanha
2
RTECS
CU6475000
Número UN
1988
Peso molecular
122.12
Beilstein
471352
Reaxy-Rn
471352
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=471352&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)

Dados de qualidade específicos do lote. Introduza o número de lote para obter o COA exato.

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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
SuperclassOrganic oxygen compounds
ClasseOrganooxygen compounds
SubclassCarbonyl compounds
Intermediate Tree Nodes Aldehydes - Aryl-aldehydes - Benzaldehydes
Direct ParentHydroxybenzaldehydes
Alternative Parents Benzoyl derivatives  1-hydroxy-2-unsubstituted benzenoids  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Hydroxybenzaldehyde - Benzoyl - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Benzenoid - Monocyclic benzene moiety - Organic oxide - Hydrocarbon derivative - Aromatic homomonocyclic compound
DescriçãoThis compound belongs to the class of organic compounds known as hydroxybenzaldehydes. These are organic aromatic compounds containing a benzene ring carrying an aldehyde group and a hydroxyl group.
External Descriptors a small molecule
Estrutura 3D
Modelo de Estrutura Química Interativa





Alvos associados (humanos)
TYR Tclin Tyrosinase (717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A1 Tclin GABA transporter 1 (308 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ABAT Tclin Gamma-amino-N-butyrate transaminase (140 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH5A1 Tclin Succinate semialdehyde dehydrogenase (19 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCHE Tclin Butyrylcholinesterase (7174 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MPO Tchem Myeloperoxidase (1002 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AOX1 Tchem Aldehyde oxidase (429 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-1080 (3966 Activities)
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MCF7 (126967 Activities)
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A549 (127892 Activities)
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T47D (39041 Activities)
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HCT-116 (91556 Activities)
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WiDr (1835 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HepG2 (196354 Activities)
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HUVEC (11049 Activities)
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KB (17409 Activities)
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HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SIRT1 Tchem NAD-dependent deacetylase sirtuin 1 (3505 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
IDO1 Tchem Indoleamine 2,3-dioxygenase (6650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SW1573 (1008 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Y79 (258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Alvos associados (não humanos)
Staphylococcus aureus (210822 Activities)
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Bacillus subtilis (32866 Activities)
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Mycobacterium tuberculosis (203094 Activities)
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Plasmodium falciparum (966862 Activities)
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Candida tropicalis (8381 Activities)
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Meloidogyne incognita (862 Activities)
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Mus musculus (284745 Activities)
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HT-22 (3261 Activities)
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B16-F10 (4610 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
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Perknaster fuscus (7 Activities)
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Cirsium arvense (30 Activities)
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Mecanismos de ação
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propriedades químicas e físicas
Ponto de inflamação (°F)345°F
Ponto de inflamação (°C)174℃
Ponto de fusão (°C)117 °C
Peso molecular122.120 g/mol
XLogP31.400
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass122.037 Da
Monoisotopic Mass122.037 Da
Topological Polar Surface Area37.300 Ų
Heavy Atom Count9
Formal Charge0
Complexity93.100
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

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