Saltar al contenido
Merck
Todas las fotos(1)

Key Documents

View All Documentation

36766

Supelco

2,6-Dimethylaniline

PESTANAL®, analytical standard

Sinónimos:

2,6-Xylidine, 2-Amino-1,3-dimethylbenzene, 2-Amino-m-xylene

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización
Todas las fotos(1)

About This Item

Fórmula lineal:
(CH3)2C6H3NH2
Número de CAS:
87-62-7
Peso molecular:
121.18
Beilstein/REAXYS Number:
636332
EC Number:
201-758-7
MDL number:
MFCD00007747
UNSPSC Code:
41116107
PubChem Substance ID:
329755502
NACRES:
NA.24

grade

analytical standard

Quality Level

100

vapor pressure

<0.01 mmHg ( 20 °C)

product line

PESTANAL®

assay

~99%

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.560 (lit.)

bp

214 °C/739 mmHg (lit.)

mp

10-12 °C (lit.)

density

0.984 g/mL at 25 °C (lit.)

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

Cc1cccc(C)c1N

InChI

1S/C8H11N/c1-6-4-3-5-7(2)8(6)9/h3-5H,9H2,1-2H3

InChI key

UFFBMTHBGFGIHF-UHFFFAOYSA-N

¿Está buscando productos similares? Visita Guía de comparación de productos

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

195.8 °F - closed cup

flash_point_c

91 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

Los clientes también vieron

Slide 1 of 6

1 of 6

4-Chloroaniline PESTANAL&#174;, analytical standard

Supelco

35823

4-Chloroaniline

Lidocaine Related Compound H United States Pharmacopeia (USP) Reference Standard

USP

1366080

Lidocaine Related Compound H

Mepivacaine hydrochloride Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1955

Mepivacaine hydrochloride

2-Octanone analytical standard

Supelco

02479

2-Octanone

2,6-Dimethylphenol PESTANAL&#174;, analytical standard

Supelco

36715

2,6-Dimethylphenol

Lidocaine Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1034

Lidocaine

Bozena Kaczmarczyk et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 68(2), 369-376 (2007-03-03)
The reaction of aniline with p-dibenzoylobenzene (K1) can lead to Z/Z, Z/E and E/E isomers however the only Z/Z and E/E were formed. At room temperature these isomers may be separated, thus the corresponding FTIR spectra could be recorded. The
Paul L Skipper et al.
Chemical research in toxicology, 19(8), 1086-1090 (2006-08-22)
Aromatic amines such as 2-naphthylamine and 4-aminobiphenyl are established human bladder carcinogens. Experimental evidence for carcinogenicity of monocylic aromatic amines is limited mostly to other organs, but a recent epidemiologic study of bladder cancer found that 2,6-dimethyl- (2,6-DMA), 3,5-dimethyl- (3,5-DMA)
Ana P Ferreira Gregorio et al.
Mycological research, 110(Pt 2), 161-168 (2006-02-21)
During the interaction of two tropical agaric fungi, Marasmius pallescens and Marasmiellus troyanus, on agar media, initial deadlock between the two mycelia was ultimately followed by take-over by M. troyanus. When shaken liquid cultures of these two fungi were mixed
Nalinrut Masomboon et al.
Journal of hazardous materials, 192(1), 347-353 (2011-06-08)
The kinetics of 2,6-dimethylaniline degradation by Fenton process, electro-Fenton process and photoelectro-Fenton process was investigated. This study attempted to eliminate the potential interferences from intermediates by making a kinetics comparison of Fenton, electro-Fenton and photoelectro-Fenton methods through use initial rate
Ming-Wei Chao et al.
Toxicological sciences : an official journal of the Society of Toxicology, 130(1), 48-59 (2012-07-27)
Several alkylanilines with structures more complex than toluidines have been associated epidemiologically with human cancer. Their mechanism of action remains largely undetermined, and there is no reported evidence that it replicates that of multicyclic aromatic amines even though the principal
Ver todos los artículos relacionados

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico