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Supelco

2,6-Dimethylaniline

PESTANAL®, analytical standard

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Synonym(s):
2,6-Xylidine, 2-Amino-1,3-dimethylbenzene, 2-Amino-m-xylene
Linear Formula:
(CH3)2C6H3NH2
CAS Number:
87-62-7
Molecular Weight:
121.18
Beilstein:
636332
EC Number:
201-758-7
MDL number:
MFCD00007747
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

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Legal Information

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

Signal Word

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 Code

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

WGK

WGK 3

Flash Point(F)

195.8 °F - closed cup

Flash Point(C)

91 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

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Wang-Ping Ting et al.
Journal of hazardous materials, 161(2-3), 1484-1490 (2008-06-17)
A new approach for promoting ferric reduction efficiency using a different electrochemical cell and the photoelectro-Fenton process has been developed to degrade organic toxic contaminants. The use of UVA light and electric current as electron donors can efficiently initiate the
Nonglak Boonrattanakij et al.
Journal of hazardous materials, 172(2-3), 952-957 (2009-08-21)
This research investigated the intrinsic second-order rate constant between 2,6-dimethyl-aniline (2,6-DMA) and hydroxyl radicals (OH) using Fenton's reactions under both batch and continuous operations. The competitive kinetics technique with aniline as a reference compound was employed. In the batch study
N W Puente et al.
Journal of analytical toxicology, 25(8), 711-715 (2002-01-05)
2,6-Dimethylaniline (2,6-xylidine; 2,6-DMA) is a nasal carcinogen in rats. Humans may be exposed to this compound via several routes: 2,6-DMA is found in cigarette smoke; it is a pharmacologically inactive metabolite of some drugs (e.g., the local anesthetic lidocaine) and
Eva Tydén et al.
Toxicological sciences : an official journal of the Society of Toxicology, 81(2), 263-272 (2004-07-16)
Whole-body low-temperature radioluminography of (3)H-2,6-xylidine in rats indicates that the nonmetabolized substance, which is a volatile and fat-soluble compound, is distributed throughout the body and accumulates in adipose tissues, e.g., in the abdominal and subcutaneous regions. Whole-body autoradiography with freeze-dried
Nalinrut Masomboon et al.
Environmental science & technology, 43(22), 8629-8634 (2009-12-24)
2,6-Dimethylaniline degradation by Fenton process has been studied in depth for the purpose of learning more about the reactions involved in the oxidation of 2,6-dimethylaniline under various reaction conditions. The effect of reaction conditions including the initial pH value, and
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