1-OCTYLIMIDAZOLE

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Company Name: Shanghai Daken Advanced Materials Co.,Ltd
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Products Intro: Product Name:1-octylimidazole
CAS:21252-69-7
Purity:>=99% Package:1KG,5KG,10KG
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Products Intro: CAS:21252-69-7
Purity:98% Package:g-Kg
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Products Intro: Product Name:1-OCTYLIMIDAZOLE
CAS:21252-69-7
Purity:97-99% Package:1KG;1USD
Company Name: AFINE CHEMICALS LIMITED
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Products Intro: Product Name:1 - OCTYL - 1H - IMIDAZOLE
CAS:21252-69-7
Purity:98%+ Package:Standard or custom package Remarks:excellent quality and reliable supplier
Company Name: Alfa Chemistry
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Products Intro: Product Name:1-octylimidazole
CAS:21252-69-7
Purity:0.98

1-OCTYLIMIDAZOLE manufacturers

  • 1-OCTYLIMIDAZOLE
  • 1-OCTYLIMIDAZOLE pictures
  • $1.00 / 1KG
  • 2019-12-20
  • CAS:21252-69-7
  • Min. Order: 1KG
  • Purity: 97-99%
  • Supply Ability: 1000KGS
1-OCTYLIMIDAZOLE Basic information
Product Name:1-OCTYLIMIDAZOLE
Synonyms:1-OCTYLIMIDAZOLE;n-octylimidazole;OIM;1H-Imidazole, 1-octyl-;1-Octylimidazole >=98.0%;SKL1369;SKL1557
CAS:21252-69-7
MF:C11H20N2
MW:180.29
EINECS:
Product Categories:
Mol File:21252-69-7.mol
1-OCTYLIMIDAZOLE Structure
1-OCTYLIMIDAZOLE Chemical Properties
Boiling point 135 °C(Press: 4 Torr)
density 0.91 g/mL at 20 °C (lit.)
refractive index n20/D1.475
storage temp. Inert atmosphere,Room Temperature
form liquid
pka7.09±0.10(Predicted)
AppearanceColorless to light yellow Liquid
BRN 122643
InChIInChI=1S/C11H20N2/c1-2-3-4-5-6-7-9-13-10-8-12-11-13/h8,10-11H,2-7,9H2,1H3
InChIKeyKLMZKZJCMDOKFE-UHFFFAOYSA-N
SMILESC1N(CCCCCCCC)C=CN=1
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26
WGK Germany 3
Storage Class10 - Combustible liquids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
1-OCTYLIMIDAZOLE Usage And Synthesis
Synthesis
Imidazole

288-32-4

1-Bromooctane

111-83-1

1-OCTYLIMIDAZOLE

21252-69-7

Imidazole (1.36 g, 20.0 mmol) was mixed with sodium hydroxide (0.80 g, 20.0 mmol) in DMSO, heated to 90 °C and maintained for 2 h, then cooled to room temperature. A DMSO solution of 1-bromooctane (3.46 g, 19.0 mmol) was added slowly and dropwise to the reaction mixture. The reaction mixture was stirred at room temperature for 3 hours and then gradually warmed to 65 °C and stirred continuously at this temperature for 16 hours. After completion of the reaction, the reaction solution was mixed with water and extracted with ether four times. The ether phases were combined and dried with anhydrous sodium sulfate. The ether was removed by distillation under reduced pressure to give Intermediate 9 as a yellow liquid (2.89 g, 89% yield).1H NMR (DMSO-d6) data were as follows: δ 7.61 (s, 2H), 7.15 (s, 1H), 6.87 (s, 1H), 3.93 (t, 2H), 1.68 (m, 2H), 1.25 (m, 10H), 0.85 (t 3H).

References[1] Synthetic Communications, 1993, vol. 23, # 13, p. 1783 - 1786
[2] Journal of Physical Chemistry B, 2013, vol. 117, # 48, p. 15014 - 15022
[3] ChemMedChem, 2017, vol. 12, # 11, p. 835 - 840
[4] Patent: WO2018/56902, 2018, A1. Location in patent: Page/Page column 32
[5] Patent: CN103951702, 2016, B. Location in patent: Paragraph 0039; 0040
1-OCTYLIMIDAZOLE Preparation Products And Raw materials
Raw materialsImidazole-->1-Bromooctane-->1-Bromoheptane-->Sodium hydroxide-->Dimethyl sulfoxide
Tag:1-OCTYLIMIDAZOLE(21252-69-7) Related Product Information
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