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Merck
CN

491799

Aniline-1-13C

99 atom % 13C

Synonym(s):

Benzenamine-1-13C

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About This Item

Empirical Formula (Hill Notation):
13CC5H7N
CAS Number:
18960-62-8
Molecular Weight:
94.12
UNSPSC Code:
12352202
PubChem Substance ID:
24872684
MDL number:
MFCD01075583
Isotopic purity:
99 atom % 13C
Assay:
99% (CP)
Mass shift:
M+1

Key Documents

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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

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

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Certificates of Analysis (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
Laya Siroos Rezaei et al.
Environmental technology, 33(19-21), 2273-2280 (2013-02-12)
Aerobic granules can be formed in sequencing batch airlift reactors (SBAR) and sequencing batch reactors (SBR). Comparing these two systems, the SBAR has excellent mixing condition, but due to a high height-to-diameter ratio (H/D), there is no performance capability at
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
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
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