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| CAS No.: | 4151-50-2 |
|---|---|
| Name: | Sulfluramid |
| Molecular Structure: | |
|
|
|
| Formula: | C10H6F17NO2S |
| Molecular Weight: | 527.202 |
| Synonyms: | AI 3-29757;Alstar;Alstar (pesticide);FX 12;FiniTron;GX 071;Mirex S;N-Ethylperfluorooctanesulfonamide;N-Ethylperfluorooctylsulfonamide;Volcano;Volcano (insecticide); |
| EINECS: | 223-980-3 |
| Density: | 1.665 g/cm3 |
| Melting Point: | 75-85 °C |
| Boiling Point: | 246.6 °C at 760 mmHg |
| Flash Point: | 102.9 °C |
| Solubility: | Insoluble (25 °C) |
| Appearance: | Tan powder |
| Hazard Symbols: |
 Xi
|
| Risk Codes: | 21-22-51/53 |
| Safety: | 36/37-61 |
| PSA: | 54.55000 |
| LogP: | 6.36430 |
- 483366-12-7(2S,4R)-1-Boc-2-cyano-4-hydroxypyrrolidine
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- 68439-39-4Poly(oxy-1,2-ethanediyl), alpha-(2-ethylhexyl)-omega-hydroxy-,
- 852475-26-4MC1568
- 43224-75-52,2,6,6-Tetramethyl-4-(2-propyleneoxy) Piperidine
- 307-35-7
perfluorooctyl sulfofluorure
- 75-04-7
ethylamine
- 4151-50-2
N-ethyl-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonamide
| Conditions | Yield |
|---|---|
| Stage #1: perfluorooctyl sulfofluorure; ethylamine With triethylamine In diethyl ether at 0 - 20℃; for 17h; Stage #2: With sodium hydrogencarbonate In diethyl ether for 3h; Heating; Further stages.; | 56% |
| In diethyl ether anhydr. ether, at -5 to 0°C, 2.75 h; | |
| With triethylamine In di-isopropyl ether for 4h; Reflux; | |
| In diethyl ether anhydr. ether, at -5 to 0°C, 2.75 h; |
- 423-60-9
perfluorooctanesulphonyl chloride
- 25152-55-0, 60435-94-1, 73602-62-7, 127322-37-6, 130089-03-1
tri-n-butylamine hydrofluoride
- 75-04-7
ethylamine
A
- 4151-50-2
N-ethyl-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonamide
| Conditions | Yield |
|---|---|
| In various solvent(s) | A 0.05 mol B 0.005 mol |
- 423-60-9
perfluorooctanesulphonyl chloride
- 75-04-7
ethylamine
A
- 4151-50-2
N-ethyl-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonamide
| Conditions | Yield |
|---|---|
| In dichloromethane Product distribution; var. solv, investigated; |
- 307-35-7
perfluorooctyl sulfofluorure
- 75-04-7
ethylamine
A
- 65756-36-7
hydrogen fluoride ethylamine
B
- 4151-50-2
N-ethyl-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonamide
| Conditions | Yield |
|---|---|
| In diethyl ether at -30-0°C,2.75 h; | |
| In diethyl ether at -30-0°C,2.75 h; |
- 4151-50-2
N-ethyl-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonamide
- 540-51-2
2-bromoethanol
- 1691-99-2
N-ethyl-N-(2-hydroxyethyl)-perfluorooctane-1-sulfonamide
| Conditions | Yield |
|---|---|
| With potassium carbonate; sodium iodide In acetone for 48h; Heating; | 99% |
- 4151-50-2
N-ethyl-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonamide
- 102229-10-7
2-(tert-butyldimethylsilyloxy)ethanol
- 1017593-64-4
1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonic acid [2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-ethyl-amide
| Conditions | Yield |
|---|---|
| With di-isopropyl azodicarboxylate; triphenylphosphine In diethyl ether at 0 - 25℃; Mitsunobu reaction; sonication; | 98% |
- 927-68-4
bromoethyl acetate
- 4151-50-2
N-ethyl-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonamide
- 1017593-63-3
2-(N-ethyl-perfluorooctylsulfonamido)ethyl acetate
| Conditions | Yield |
|---|---|
| With potassium carbonate; sodium iodide In acetone for 36h; Heating; | 92% |
- 4151-50-2
N-ethyl-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonamide
- 96-32-2
bromoacetic acid methyl ester
- 87988-69-0
methyl 2-(N-ethyl-perfluorooctanesulfonamido) acetate
| Conditions | Yield |
|---|---|
| With potassium carbonate; sodium iodide In acetone for 3h; Heating; | 90% |
- 108-77-0
1,3,5-trichloro-2,4,6-triazine
- 4151-50-2
N-ethyl-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonamide
| Conditions | Yield |
|---|---|
| Stage #1: N-ethyl-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonamide With sodium In ethanol for 0.5h; Metallation; Stage #2: 1,3,5-trichloro-2,4,6-triazine In acetone at -78 - 20℃; for 2h; Substitution; | 72% |
- 96-35-5
glycolic acid methyl ester
- 4151-50-2
N-ethyl-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonamide
- 87988-69-0
methyl 2-(N-ethyl-perfluorooctanesulfonamido) acetate
| Conditions | Yield |
|---|---|
| With di-isopropyl azodicarboxylate; triphenylphosphine In diethyl ether at 0 - 25℃; Mitsunobu reaction; sonication; | 67% |
This product is a nationally controlled contraband, and the Lookchem platform doesn't provide relevant sales information.
Chemistry
Empirical Formula: C10H6F17NO2S
Molecular Weight: 527.198 g/mol
EINECS: 223-980-3
Index of Refraction: 1.32
Density: 1.665 g/cm3
Flash Point: 102.9 °C
Melting point: 75-85 °C
Appearance: Tan powder
Enthalpy of Vaporization: 48.37 kJ/mol
Boiling Point: 246.6 °C at 760 mmHg
Vapour Pressure: 0.0269 mmHg at 25 °C
Structure of Sulfluramid (CAS NO.4151-50-2):
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IUPAC Name: N-Ethyl-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonamide
Product Category of Sulfluramid (CAS NO.4151-50-2): Organics;Sulfur & Selenium Compounds;Pesticide & intermediate;Metal Isotopes
Uses
Sulfluramid (CAS NO.4151-50-2) can be used as emulsifier, wetting agent, and organic fluorine.
Toxicity Data With Reference
| Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
|---|---|---|---|---|---|
| quail | LD50 | oral | 473mg/kg (473mg/kg) | Pesticide Manual. Vol. 9, Pg. 773, 1991. | |
| rat | LD50 | oral | 543mg/kg (543mg/kg) | Pesticide Manual. Vol. 9, Pg. 773, 1991. |
Safety Profile
Hazard Codes: 
Xi
Hazard Note: Irritant
Specification
Sulfluramid , its cas register number is 4151-50-2. It also can be N-Ethyl perfluorooctanesulfonamide ; and N-Ethyl-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluoro-octanesulfonamide .