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Merck

488100

Aniline-15N

98 atom % 15N

Sinónimos:

Benzenamine-15N

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1 G

MXP 8,682.00

MXP 8,682.00

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Fórmula lineal:
C6H515NH2
Número CAS:
7022-92-6
Peso molecular:
94.12
MDL number:
MFCD00084195
UNSPSC Code:
12352116
PubChem Substance ID:
24872331
NACRES:
NA.12

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isotopic purity

98 atom % 15N

Quality Level

200

assay

99% (CP)

refractive index

n20/D 1.586 (lit.)

bp

184 °C (lit.)

mp

−6 °C (lit.)

density

1.033 g/mL at 25 °C

mass shift

M+1

storage temp.

2-8°C

SMILES string

[15NH2]c1ccccc1

InChI

1S/C6H7N/c7-6-4-2-1-3-5-6/h1-5H,7H2/i7+1

InChI key

PAYRUJLWNCNPSJ-CDYZYAPPSA-N

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1 of 4

Este artículo
491799488208485497
Aniline-15N 98 atom % 15N

Sigma-Aldrich

488100

Aniline-15N

Aniline-1-13C 99 atom % 13C

Sigma-Aldrich

491799

Aniline-1-13C

Benzylamine-15N 98 atom % 15N

Sigma-Aldrich

488208

Benzylamine-15N

Aniline-13C6 99 atom % 13C

Sigma-Aldrich

485497

Aniline-13C6

mass shift

M+1

mass shift

M+1

mass shift

M+1

mass shift

M+6

assay

99% (CP)

assay

99% (CP)

assay

99% (CP)

assay

99% (CP)

isotopic purity

98 atom % 15N

isotopic purity

99 atom % 13C

isotopic purity

98 atom % 15N

isotopic purity

99 atom % 13C

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

density

1.033 g/mL at 25 °C

density

1.033 g/mL at 25 °C

density

0.990 g/mL at 25 °C

density

1.087 g/mL at 25 °C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

-

storage temp.

2-8°C

Packaging

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.

signalword

Danger

Hazard Classifications

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

Clase de almacenamiento

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

wgk_germany

WGK 3

flash_point_f

158.0 °F - closed cup

flash_point_c

70 °C - closed cup

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Certificados de análisis (COA)

Lot/Batch Number
MBBD6217
MBBC9841
BGBC4580V
MBBB1297V
EB0980

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Conghui Tang et al.
Journal of the American Chemical Society, 134(46), 18924-18927 (2012-11-08)
A novel and efficient copper-catalyzed azidation reaction of anilines via C-H activation has been developed. This method, in which the primary amine acts as a directing group by coordinating to the metal center, provides ortho azidation products regioselectively under mild
Sung Jin Bae et al.
European journal of medicinal chemistry, 57, 383-390 (2012-11-15)
We attempted to design and synthesize (E)-N-substituted benzylidene-hydroxy or methoxy-aniline derivatives and to evaluate their inhibitory effect on tyrosinase activity and anti-melanogenesis activity in murine B16F10 melanoma cells. Derivatives with a 4-methoxy- or 4-hydroxy-anilino group exerted more potent inhibition against
Huihui Yang et al.
Electrophoresis, 34(4), 510-517 (2012-11-23)
A novel (3-sulfopropyl methacrylate potassium)-silica hybrid monolithic column for CEC has been prepared by a simple one-pot approach based on efficient thiol-ene click chemistry. In this process, the polycondensation of hydrolyzed alkoxysilanes and in situ click reaction of vinyl groups
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
Dongdong Liang et al.
Chemical communications (Cambridge, England), 49(2), 173-175 (2012-11-22)
An efficient synthesis of free (NH)-phenanthridinones through Pd-catalyzed C(sp(2))-H aminocarbonylation of unprotected o-arylanilines under an atmospheric pressure of CO has been developed. Some ortho heteroarene substituted anilines as well as N-alkyl protected o-arylanilines are also suitable substrates for this C-H
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