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49636

Supelco

N-Methylaniline

analytical standard

Sinonimo/i:

Monomethylaniline

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About This Item

Formula condensata:
C6H5NHCH3
Numero CAS:
100-61-8
Peso molecolare:
107.15
Beilstein:
741982
Numero CE:
202-870-9
Numero MDL:
MFCD00008283
Codice UNSPSC:
41116107
ID PubChem:
329757499
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Saggio

≥98.5%

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Indice di rifrazione

n20/D 1.571 (lit.)
n20/D 1.571

P. ebollizione

196 °C (lit.)

Punto di fusione

−57 °C (lit.)

Densità

0.989 g/mL at 25 °C (lit.)

applicazioni

environmental

Formato

neat

Stringa SMILE

CNc1ccccc1

InChI

1S/C7H9N/c1-8-7-5-3-2-4-6-7/h2-6,8H,1H3
AFBPFSWMIHJQDM-UHFFFAOYSA-N

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Categorie correlate

Applicazioni

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Avvertenze

Danger

Indicazioni di pericolo

H301 + H311 + H331,H319,H373,H410

Classi di pericolo

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - STOT RE 2 Oral

Organi bersaglio

Liver,spleen,Bone marrow

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

185.0 °F - closed cup

Punto d’infiammabilità (°C)

85 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
BCCF9518
BCBZ7926
BCBV3692
BCBT2462

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Sigma-Aldrich

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Supelco

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N,N-Dimethylaniline ReagentPlus®, 99%

Sigma-Aldrich

515124

N,N-Dimethylaniline

Cloroformio anhydrous, ≥99%, contains 0.5-1.0% ethanol as stabilizer

Sigma-Aldrich

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Sodium hydrosulfite technical grade

Sigma-Aldrich

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Sodium hydrosulfite

Anita Horváth et al.
Steroids, 71(8), 706-711 (2006-06-06)
Efficient ring opening of steroidal 2,3-epoxides with stoichiometric amount of aromatic amines has been carried out using an ionic liquid ([bmim](+)[BF(4)](-)) both as solvent and catalyst. The reactions were completely regio- and stereoselective in each case. The aminoalcohol products have
Allison G Condie et al.
ChemMedChem, 7(12), 2194-2203 (2012-11-09)
Myelination is a fundamental biological process in the vertebrate nervous system. Damage to or malformation of myelin can lead to various neurological diseases; for example, demyelination in the spinal cord is a major cause of paralysis of patients suffering from
V Arjunan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 72(2), 436-444 (2008-12-17)
The Fourier transform infrared (FTIR) and FT-Raman spectra of 2-chloro-4-methylaniline and 2-chloro-6-methylaniline have been measured in the range 4000-400 and 4000-100cm(-1), respectively. Utilising the observed FTIR and FT-Raman data, a complete vibrational assignment and analysis of the fundamental modes of
S Ramalingam et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 76(1), 84-92 (2010-03-26)
The FTIR and FTRaman spectra of 2-bromo-4-methyl aniline (2-B-4-MA) molecule have been recorded using Brucker IFS 66V spectrometer in the range of 4000-100 cm(-1). The molecular geometry and vibrational frequencies in the ground state are calculated using the Hartree-Fock (HF)
V Kameshwara Rao et al.
Bioorganic & medicinal chemistry letters, 21(12), 3511-3514 (2011-05-27)
An efficient and economical method was developed for the synthesis of 3-substituted indoles by one-pot three-component coupling reaction of a substituted or unsubstituted benzaldehyde, N-methylaniline, and indole or N-methylindole using Yb(OTf)(3)-SiO(2) as a catalyst. All the synthesized compounds were evaluated
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