3-Isobutylaniline

3-Isobutylaniline Suppliers list
Company Name: Shanghai Raise Chemical Technology Co.,Ltd  
Tel: 15026594951
Email: rs@raise-chem.com
Company Name: Zouping Mingxing Chemical Co.,Ltd.  
Tel: 86-13605431940 13605431940
Email: zpmxchemical@126.com
Company Name: Mashilabs (Shanghai) Co.,Ltd.  
Tel: 19916721580
Email: mafarm@126.com
Company Name: Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.  
Tel: 025-66028182 17714375163
Email: yftan@aikonchem.com
Company Name: Suzhou Nuoouman Biological Technology Co., Ltd.  
Tel: 15026866316
Email: 180642609@qq.com

3-Isobutylaniline manufacturers

  • 3-Isobutylaniline
  • 3-Isobutylaniline pictures
  • $6.60
  • 2019-12-31
  • CAS:131826-11-4
  • Min. Order: 1KG
  • Purity: 97%-99%
  • Supply Ability: 1kg-1000kg
3-Isobutylaniline Basic information
Product Name:3-Isobutylaniline
Synonyms:3-Isobutylaniline;Benzenamine, 3-(2-methylpropyl)-;3-(2-Methylpropyl)aniline;3-(2-methylpropyl)-Benzenamine
CAS:131826-11-4
MF:C10H15N
MW:149.23
EINECS:
Product Categories:
Mol File:131826-11-4.mol
3-Isobutylaniline Structure
3-Isobutylaniline Chemical Properties
Boiling point 245.7±9.0 °C(Predicted)
density 0.944±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka4.60±0.10(Predicted)
Safety Information
HS Code 2921490090
MSDS Information
3-Isobutylaniline Usage And Synthesis
Uses3-Isobutylaniline (cas# 131826-11-4) is a useful research chemical. It is used in the development of novel carboxanilide acaricide, pyflubumide that exhibits excellent acaricidal activity against Tetranychus and Panonychus species.
Synthesis
Benzene, 1-(2-methyl-1-propenyl)-3-nitro-

6026-73-9

3-Isobutylaniline

131826-11-4

The general procedure for the synthesis of 3-isobutylaniline from the compound (CAS: 6026-73-9) was as follows: in a 50 mL round bottom flask, 0.976 g of the oil obtained in Example 11, 1.60 g (15.0 mmol) of sodium hypophosphite monohydrate, 0.27 g (2.5 mmol) of sodium carbonate, and 115 mg of palladium(0)/carbon catalyst ( 5% loading, 50% water content). Subsequently, 2.5 mL of n-butyl acetate and 2.5 mL of water were added and the mixture was reacted under reflux conditions for 3 hours. Upon completion of the reaction, the mixture was processed as in Example 12 and the organic layer was quantitatively analyzed by HPLC internal standard method to yield 0.698 g of 3-isobutyryl aniline (1) (Analytical Condition A). The yield was 93% based on 1-bromo-3-nitrobenzene.

References[1] Patent: JP2017/14131, 2017, A. Location in patent: Paragraph 0049
[2] Patent: US5212320, 1993, A
3-Isobutylaniline Preparation Products And Raw materials
Raw materialsBenzene, 1-(2-methyl-1-propenyl)-3-nitro--->Palladium-->Water-->Sodium carbonate-->Sodium hypophosphite monohydrate-->Butyl acetate
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