491799
苯胺-1-13C
99 atom % 13C
别名:
Benzenamine-1-13C
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关于此项目
经验公式（希尔记法）:
13CC5H7N
化学文摘社编号:
分子量:
94.12
UNSPSC Code:
12352202
PubChem Substance ID:
MDL number:
Isotopic purity:
99 atom % 13C
Assay:
99% (CP)
Mass shift:
M+1
InChI
1S/C6H7N/c7-6-4-2-1-3-5-6/h1-5H,7H2/i6+1
SMILES string
N[13c]1ccccc1
InChI key
PAYRUJLWNCNPSJ-PTQBSOBMSA-N
isotopic purity
99 atom % 13C
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
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
存储类别
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
法规信息
新产品
此项目有
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
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
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
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
Huaxian Ma et al.
Toxicology and applied pharmacology, 267(3), 276-283 (2013-01-29)
Mechanisms by which aniline exposure elicits splenotoxicity, especially a tumorigenic response, are not well-understood. Earlier, we have shown that aniline exposure leads to oxidative DNA damage and up-regulation of OGG1 and NEIL1/2 DNA glycosylases in rat spleen. However, the contribution
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