• 原料直供
• 试剂商城
• 直接询价

分类

• {SNA} Building Blocks, Chemical Synthesis, Nitrogen Compounds, Organic Building Blocks, Protected Amines
• {uni_hamburg} no charge; carbocycle; aromatic; 6RingOnly; 6ring; amide; 1fragment

相关文献及参考

• Short: EINECS Title: EINECS (European Inventory of Existing Commercial Chemical Substances) Source: Official Journal of the European Communities Volume: C 146 A (15.06.1990) Page: 1 Year: 1990 Internet Resource: http://ecb.jrc.ec.europa.e
• Short: III/35D2 Title: Nuclear Magnetic Resonance (NMR) Data: Chemical Shifts for Carbon-13, Part 2: Aromatic Compounds Author: Mikhova, B. Editor: Gupta, R.R.; Lechner, M.D. Source: Landolt-Börnstein, New Series Volume: III/35D2 Year: 2005 Keyword: aromatic compounds; carbon-13; chemical shift; coupling constant; molecular structure ISBN: 978-3-540-20189-2 ISBN: 3-540-20189-0 Internet Resource: DOI:10.1007/b83345 RefComment: VIII, 291 p., Hardcover RefComment: Written for Science and engineers in the fields of physics, chemistry and physical chemistry who inted to use NMR to study the structure and the binding of molecules Abstract: Nuclear Magnetic Resonance (NMR) is based on the fact that certain nuclei exhibit a magnetic moment, orient by a magnetic field, and absorb characteristic frequencies in the radiofrequency part of the spectrum. The spectral lines of the nuclei are highly influenced by the chemical environment i.e. the structure and interaction of the molecules. NMR is now the leading technique and a powerful tool for the investigation of the structure and interaction of molecules. The present Landolt-Börnstein volume III/35 Nuclear Magnetic Resonance (NMR) Data is therefore of major interest to all scientists and engineers who intend to use NMR to study the structure and the binding of molecules. Volume III/35 "NMR-Data" is divided into several subvolumes and parts. Subvolume III/35A contains the nuclei 11B and 31P, subvolume III/35B contains the nuclei 19F and 15N, subvolume III/35C contains the nucleus 1H, subvolume III/35D contains the nucleus 13C, subvolume III/35E contains the nucleus 17O, and subvolume III/35G contains the nucleus 77Se. More nuclei will be presented later.

安全信息

GHS Symbol

TYPE OF TEST            : LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE       : Intravenous
SPECIES OBSERVED        : Rodent - mouse
DOSE/DURATION           : 320 mg/kg
TOXIC EFFECTS :
   Details of toxic effects not reported other than lethal dose value
REFERENCE :
   CSLNX* U.S. Army Armament Research & Development Command, Chemical Systems
   Laboratory, NIOSH Exchange Chemicals.  (Aberdeen Proving Ground, MD 21010)
   Volume(issue)/page/year: NX#02899

TYPE OF TEST            : Mutation in microorganisms
TEST SYSTEM             : Bacteria - Salmonella typhimurium
DOSE/DURATION           : 333 ug/plate
REFERENCE :
   EMMUEG Environmental and Molecular Mutagenesis.  (Alan R. Liss, Inc., 41 E.
   11th St., New York, NY 10003)  V.10-    1987-  Volume(issue)/page/year:
   11(Suppl 12),1,1988

其他信息

• 下游产品:活性金黄KM-G --> 活性金黄 K-2RA --> 活性黄3 --> 活性黄KE-RN --> 酸性兰BGL
• 图谱信息:间氨基乙酰苯胺(102-28-3)质谱(MS) 间氨基乙酰苯胺(102-28-3)红外图谱(IR2) 间氨基乙酰苯胺(102-28-3)红外图谱(IR1)
• 用途一:主要用作反应染料和分散染料的中间体
• 间氨基乙酰苯胺价格(试剂级):更新日期 产品编号 产品名称 包装 价格 2014/06/02 A1533 3'-氨基乙酰苯胺 3'-Aminoacetanilide 25G 209元 2014/06/02 A1533 3'-氨基乙酰苯胺 3'-Aminoacetanilide 500G 891元 2010/06/21 344150050 间氨基乙酰苯胺 3'-Aminoacetanilide 98% 5 GR 390元
• 毒性分级:中毒
• 急性毒性:静脉-小鼠LD50: 320 毫克/公斤
• MSDS 信息:N1-(3-Aminophenyl)acetamide(102-28-3).msds
• 方法一:由间苯二胺酰化而得。向反应锅中加入水及间苯二胺，使溶解。再加入30%盐酸，搅拌半小时，然后加入乙酸，控制反应温度在40℃，保温搅拌1h，加入精盐盐析，过滤。经中和得间氨基乙酰苯胺。酰化操作也可能采用乙酐作为原料。原料消耗定额间苯二胺1021kg/t、乙酐1013kg/t、盐酸475kg/t。
• Acros Organics:3-氨基乙酰苯胺 3'-Aminoacetanilide, 98%(102-28-3)
• 用途二:染料中间体。主要用于制备活性黄K-RN及分散染料。
• 上游原料:乙酸 --> 间苯二胺 --> 3-硝基苯胺 --> 硫化钙
• MOL 文件:102-28-3.mol
• 可燃性危险特性:可燃;燃烧产生有毒氮氧化物烟雾
• 灭火剂:干粉、泡沫、砂土、二氧化碳, 雾状水
• 刺激数据:眼睛-兔子 500 毫克/24小时 重度
• 储运特性:库房通风低温干燥
• TCI Shanghai:3'-氨基乙酰苯胺 3'-Aminoacetanilide,>;98.0%(LC)(T)(102-28-3)
• Sigma Aldrich:102-28-3(sigmaaldrich)
• 类别:有毒物品