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491799

Sigma-Aldrich

Aniline-1-13C

99 atom % 13C

Sinônimo(s):

Benzenamine-1-13C

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About This Item

Fórmula empírica (Notação de Hill):
13CC5H7N
Número CAS:
18960-62-8
Peso molecular:
94.12
Número MDL:
MFCD01075583
Código UNSPSC:
12352202
ID de substância PubChem:
24872684

pureza isotópica

99 atom % 13C

Nível de qualidade

200

Ensaio

99% (CP)

índice de refração

n20/D 1.586 (lit.)

p.e.

184 °C (lit.)

pf

−6 °C (lit.)

densidade

1.033 g/mL at 25 °C

alteração de massa

M+1

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

N[13c]1ccccc1

InChI

1S/C6H7N/c7-6-4-2-1-3-5-6/h1-5H,7H2/i6+1

chave InChI

PAYRUJLWNCNPSJ-PTQBSOBMSA-N

Categorias relacionadas

Embalagem

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Dam. 1 - Muta. 2 - Resp. Sens. 1

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

158.0 °F - closed cup

Ponto de fulgor (°C)

70 °C - closed cup

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Certificados de análise (COA)

Lot/Batch Number
EB2439
TV0694
13975HS
12878EU
IS0606

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Ronald Besandre et al.
Organic letters, 15(7), 1666-1669 (2013-03-15)
N-substituted indoles are synthesized from primary amines through a tandem reaction sequence. Initial condensation of the amine with an α-(o-haloaryl)ketone or aldehyde is followed by intramolecular aryl amination catalyzed by CuI. A variety of anilines and alkyl amines, including those
Roman Spesyvtsev et al.
Faraday discussions, 157, 165-179 (2012-12-13)
Femtosecond time-resolved photoelectron imaging is employed to investigate ultrafast electronic relaxation in aniline, a prototypical aromatic amine. The molecule is excited at wavelengths between 269 and 238 nm. We observe that the S2(pi3s/pi sigma*) state is populated directly during the
Wen Chen et al.
Journal of the American Chemical Society, 135(11), 4438-4449 (2013-03-02)
A series of linear and cyclic, sequence controlled, DNA-conjoined copolymers of aniline (ANi) and 2,5-bis(2-thienyl)pyrrole (SNS) were synthesized. In one approach, linear copolymers were prepared from complementary DNA oligomers containing covalently attached SNS and ANi monomers. Hybridization of the oligomers
A Subashini et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 104, 403-408 (2013-01-01)
One of the Schiff base 4-bromo-4'dimethylamino benzylideneaniline (BDMABA) compounds was synthesized and single crystal of the material was grown by solvent evaporation method at room temperature. Molecular structure of BDMABA was confirmed by (1)H nuclear magnetic resonance and the presence
Timo Stahl et al.
Journal of the American Chemical Society, 135(4), 1248-1251 (2013-01-15)
Heterolytic splitting of the Si-H bond mediated by a Ru-S bond forms a sulfur-stabilized silicon cation that is sufficiently electrophilic to abstract fluoride from CF(3) groups attached to selected anilines. The ability of the Ru-H complex, generated in the cooperative
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