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Merck
CN

586765

苯胺-4-13C

99 atom % 13C

别名:

Benzenamine-4-13C

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关于此项目

线性分子式:
13CC5H4NH2
化学文摘社编号:
分子量:
93.11
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
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同位素纯度

99 atom % 13C

沸点

184 °C (lit.)

mp

-6 °C (lit.)

密度

1.033 g/mL at 25 °C

质量偏移

M+1

储存温度

2-8°C

SMILES字符串

Nc1cc[13cH]cc1

InChI

1S/C6H7N/c7-6-4-2-1-3-5-6/h1-5H,7H2/i1+1

InChI key

PAYRUJLWNCNPSJ-OUBTZVSYSA-N

一般描述

Aniline-4-13C 99 atom % 13C is a high-purity isotope product with a unique chemical profile that belongs to the class of isotopes. Produced by Sigma-Aldrich, we are committed to providing quality isotope products and a reliable supply chain. Available in industrial and pre-pack quantities.

应用

- High-resolution NMR spectroscopy
- Metabolomic profiling and pathway analysis
- Stable Isotope probing in Environmental microbiology
- reaction mechanism investigations

特点和优势

Features
  • Cutting-edge technology in production.
  • Comprehensive support and documentation provided.
  • Flexible ordering options for different scales.
  • Expert technical assistance available.


Benefits
  • Streamlines the synthesis of complex molecules.
  • Supports innovative approaches in organic chemistry.
  • Enhances the efficiency of chemical reactions.
  • Facilitates the development of new therapeutic agents.

包装

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.

警示用语:

Danger

危险分类

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

储存分类代码

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

WGK

WGK 3

闪点(°F)

168.8 °F - closed cup

闪点(°C)

76 °C - closed cup


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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.
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
Ping-Xin Zhou et al.
Chemical communications (Cambridge, England), 49(31), 3254-3256 (2013-03-14)
Isoindolines are synthesized by palladium-catalyzed coupling reaction of N-(2-iodobenzyl) anilines with α,β-unsaturated N-tosylhydrazones. The reaction has several potential advantages: (1) toleration of a wide range of functional groups, (2) easy to handle and with mild conditions, (3) enriches the isoindoline
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

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