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Merck
CN

488100

Aniline-15N

98 atom % 15N

Synonym(s):

Benzenamine-15N

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About This Item

Linear Formula:
C6H515NH2
CAS Number:
7022-92-6
Molecular Weight:
94.12
NACRES:
NA.12
PubChem Substance ID:
24872331
UNSPSC Code:
12352116
MDL number:
MFCD00084195

Key Documents

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Product Name

Aniline-15N, 98 atom % 15N

InChI

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

SMILES string

[15NH2]c1ccccc1

InChI key

PAYRUJLWNCNPSJ-CDYZYAPPSA-N

isotopic purity

98 atom % 15N

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

Quality Level

200

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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.

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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

Storage Class

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

wgk

WGK 3

flash_point_f

158.0 °F - closed cup

flash_point_c

70 °C - closed cup

Regulatory Information

危险化学品
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Certificates of Analysis (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
Yu Qian et al.
Chemical communications (Cambridge, England), 49(26), 2700-2702 (2013-02-26)
An enantioselective four-component reaction of a diazoketone, water, an aniline and ethyl glyoxylate in the presence of catalytic Rh2(OAc)4 and a chiral Brønsted acid was developed to efficiently produce β-hydroxy-α-amino acid derivatives in good yields with high diastereoselectivity and enantioselectivity.
Rongjun He et al.
Chemical communications (Cambridge, England), 49(20), 2064-2066 (2013-02-06)
Mycobacterium protein tyrosine phosphatase B (mPTPB) is essential for the survival and persistence of Mycobacterium in the host. Thus small molecule inhibitors of mPTPB are potential anti-TB agents. We developed an efficient organocatalytic multicomponent reaction (MCR) between pyrrole, formaldehyde and
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