| Company Name: |
Alchemie Shanghai Co.,Ltd. |
| Tel: |
+8615921545397 |
| Email: |
cindy_hu@alchemie-shanghai.com |
| Products Intro: |
Product Name:2,6-Diethylaniline;Benzenamine, 2,6-diethyl-;2,6-Diethylbenzenamine;Aniline, 2,6-diethyl-;2,6-Diethyl aniline;2,6-diethylphenylamine;2,6-Diethyl-Benzenamine;(2,6-diethyl-phenyl)-amine;26DEA
CAS:579-66-8
Purity:100% Package:-
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- 2,6-Diethylaniline
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- $100.00 / 200KG
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2026-05-18
- CAS:579-66-8
- Min. Order: 200KG
- Purity: 99%
- Supply Ability: 20ton
- 2,6-Diethylaniline
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- $0.00 / 25KG
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2025-12-01
- CAS:579-66-8
- Min. Order: 1KG
- Purity: 98.0%
- Supply Ability: 10000KGS
- 2,6-Diethylaniline
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- $1.10 / 1g
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2025-11-18
- CAS:579-66-8
- Min. Order: 1g
- Purity: 99.00%
- Supply Ability: 100 Tons Min
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| | 2,6-Diethylaniline Basic information |
| Product Name: | 2,6-Diethylaniline | | Synonyms: | 2,6-Diethylaniline,2-Amino-1,3-diethylbenzene;2,6-Diethylaniline, 98% 1LT;2,6-diethyl-anilin;2,6-diethyl-benzenamin;2,6-Diethylbenzenamine;2,6-diethyl-Benzenamine;DEA) 2,6-Diethy;2,6- twoethyl aniline | | CAS: | 579-66-8 | | MF: | C10H15N | | MW: | 149.23 | | EINECS: | 209-445-7 | | Product Categories: | Organics;Aniline Derivatives;o-alkylated Anilines;Intermediates of Dyes and Pigments | | Mol File: | 579-66-8.mol |  |
| | 2,6-Diethylaniline Chemical Properties |
| Melting point | 3-4 °C | | Boiling point | 243 °C (lit.) | | density | 0.906 g/mL at 25 °C (lit.) | | vapor pressure | 0.02 mm Hg ( 20 °C) | | refractive index | n20/D 1.545(lit.) | | Fp | 254 °F | | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | | solubility | Chloroform (Slightly), Methanol (Slightly) | | form | Liquid | | pka | 4.13±0.10(Predicted) | | color | Clear yellow to reddish-brown | | Water Solubility | 0.67g/L(26.7 ºC) | | Sensitive | Air Sensitive | | BRN | 1423626 | | Henry's Law Constant | 8.8×100 mol/(m3Pa) at 25℃, Duchowicz et al. (2020) | | Stability: | Air Sensitive | | InChI | 1S/C10H15N/c1-3-8-6-5-7-9(4-2)10(8)11/h5-7H,3-4,11H2,1-2H3 | | InChIKey | FOYHNROGBXVLLX-UHFFFAOYSA-N | | SMILES | CCc1cccc(CC)c1N | | CAS DataBase Reference | 579-66-8(CAS DataBase Reference) | | NIST Chemistry Reference | Benzenamine, 2,6-diethyl-(579-66-8) | | EPA Substance Registry System | 2,6-Diethylaniline (579-66-8) |
| Hazard Codes | Xn | | Risk Statements | 22 | | Safety Statements | 23-24 | | RIDADR | 2810 | | WGK Germany | 2 | | RTECS | BX3500000 | | F | 8-9-23 | | TSCA | TSCA listed | | HazardClass | 6.1(b) | | PackingGroup | III | | HS Code | 29214200 | | Storage Class | 10 - Combustible liquids | | Hazard Classifications | Acute Tox. 4 Oral | | Hazardous Substances Data | 579-66-8(Hazardous Substances Data) |
| | 2,6-Diethylaniline Usage And Synthesis |
| Chemical Properties | Clear liquid | | Uses | 2,6-Diethylaniline is used as a reagent in the synthesis of herbicides, for instance Butachlor (B689925); a pre-emergent chloroacetanalide herbicide commonly used for weed control in rice as well as cotton, maize, wheat and other crops. | | Production Methods | 2,6-Diethylaniline is obtained in high yield when aniline is heated with ethylene at 200-300°C under high pressure in the presence of aluminum anilide (Northcott 1978). | | General Description | The 2,6-diethylaniline complexes with iodine, as a sigma-acceptor, were studied spectrophotometrically in chloroform, dichloromethane and carbontetrachloride solutions. It is an intermediate for the production of alachlor, butachlor, metolachlor-herbicides, tiafentiurone-insecticide, carbodiimide and RIM-PUR. | | Industrial uses | 2,6-Diethylaniline is used in the synthesis of herbicides such as Nevirex G and butachlor (Vertesi and Miklos 1982; Lee et al 1982). | | Metabolic pathway | Incubation of 2,6-diethylaniline (DEA) with NADPH-
fortified rat liver microsomal enzymes produces 4-
amino-3,5-diethylphenol (ADEP) as the major
oxidation product. ADEP is shown to undergo further
oxidation to 3,5-diethylbenzoquinone-4-imine (DEBQI),
which is isolated as a minor metabolite during DEA
oxidation. | | Metabolism | Incubation of 2,6-diethylaniline with NADPH-fortified microsomes produced 4-amino-3,5-diethylphenol (ADEP) as the major oxidation product (Feng and Wratten 1987). ADEP underwent further oxidation to 3,5-diethyl-benzoquinone-4-imine which is isolated as a minor metabolite during 2,6-diethylaniline metabolism. 2,6-Diethylaniline is produced under aerobic soil conditions as a minor metabolite of the herbicide butachlor (Lee et al 1982). 2,6-Diethylaniline is degraded by the soil microorganism Chaetomium globosum to 2,6-diethylacetanilide and 2,6-diethyl-p-benzoquinone (Lee and Ryu 1982). 2,6-Diethylaniline was also very persistent towards biodegradation in pond water with and without sewage sludge inoculation (Lyons et al 1985). |
| | 2,6-Diethylaniline Preparation Products And Raw materials |
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