Catechol solution - analytical standard, 1000ug/ml in methanol , CAS No.120-80-9

CAS: 120-80-9 Cat. No.: C117392 Fórmula: C6H6O2 Peso molecular: 110.11 Beilstein Registry Number: 471401 Número EC: 204-427-5
Disponible para pedir
CALIDAD & PUREZA Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. 1000ug/ml in methanol
Synonyms
Pyrocatechol|1,2-Benzenediol|1,2-Dihydroxybenzene|o-dihydroxybenzene
Storage
Protected from light,Room temperature
Shipped In
FedEx DG Service
★
Talla
USA
Alemania (EU)*
Precio
Cantidad
2ml
C117392-2ml
Fabricado bajo pedido · 8–12 semanas
63,90US$
Enter a quantity for the sizes you want to add.

Especificaciones

Sinónimos
Pyrocatechol | 1,2-Benzenediol | 1,2-Dihydroxybenzene | o-dihydroxybenzene
Especificaciones y pureza
analytical standard, 1000ug/ml in methanol
Condiciones de almacenamiento de almacenamiento
Protected from light,Room temperature
Enviado en
FedEx DG Service
Grado
Analytical standard
Nombres e identificadores
Sonrisas canónicas
Oc1ccccc1O
InChIKey
YCIMNLLNPGFGHC-UHFFFAOYSA-N
INCHI
1S/C6H6O2/c7-5-3-1-2-4-6(5)8/h1-4,7-8H
Isómeros SMILES
C1=CC=C(C(=C1)O)O
WGK Alemania
2
RTECS
UX1050000
Número ONU
2811
Grupo de embalaje
I
Peso molecular
110.11
Beilstein
471401
Reaxy-Rn
471401
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=471401&ln=

Datos avanzados

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClasePhenols
SubclassBenzenediols
Intermediate Tree Nodes Not available
Direct ParentCatechols
Alternative Parents 1-hydroxy-4-unsubstituted benzenoids  1-hydroxy-2-unsubstituted benzenoids  Benzene and substituted derivatives  Organooxygen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Catechol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as catechols. These are compounds containing a 1,2-benzenediol moiety.
External Descriptors a catechol
Estructura 3D
Modelo de Estructura Química Interactiva





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.

5 results found

Lot NumberCertificate TypeFechaArticulo
G2610286G2610286Certificate of AnalysisJul 02, 2026 C117392
K2528192K2528192Certificate of AnalysisNov 24, 2025 C117392
I2126011I2126011Certificate of AnalysisApr 03, 2025 C117392
H2219086H2219086Certificate of AnalysisJul 23, 2022 C117392
C2208295C2208295Certificate of AnalysisJan 19, 2022 C117392
Propiedades químicas y físicas
SensibilidadLight sensitive.
Punto de inflamación (°F)260.6 °F - closed cup
Punto de inflamación (°C)127°C- closed cup
Punto de ebullición (°C)245°C
Punto de fusión (°C)100-103 °C (lit.)
Preguntas frecuentes y artículos
Tyrosinase: a key regulatory enzyme in melanin synthesis and its biological and applied significance
Strategies and Progress in the Asymmetric Catalytic Synthesis of Chiral 1,2-Bis(boronic) Esters: Route Types, Selectivity Challenges, and Sequential Site Utilization (with Product Selection Navigator and Tables 1–4)
Choosing Boron Sources to Make Reactions Robust: How Boronic Acids, Boronate Esters, BF₃K Salts, and MIDA Improve Suzuki–Miyaura Start-Up and Scale-Up Reproducibility (with Product Tables 1–5)
Enzymatic Hydroxylation Mechanism of Salicylate Conversion to Catechol
The Chemical Basis of Natural Lacquer Durability: Urushiol Structure, Oxidative Polymerization Film Formation, and Coating Film Properties
Electron Transfer and Nucleophilic Reactions of Benzoquinones: Effects of the Conjugated Dicarbonyl Structure, Substituents, and Medium
Citations of This Product
Calculadoras de soluciones
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