Specifications
- Purity
- ≥98% (HPLC)
- Appearance
- Off-white solid
- Identity
- 1H-NMR
Properties
- Solvents
- acetone, toluene, ethanol, water (practically insoluble)
- Melting Point
- 138-148°C
- Density
- 1.70 g/cm3 at 20°C
Available from stock
Tralomethrin
- SKU
- T0116
Category: Insecticides
- Synonyms
- (S)-α-Cyano-3-phenoxybenzyl (1R,3S)-2,2-dimethyl-3-[(RS)-1,2,2,2-tetrabromoethyl]cyclopropanecarboxylate
- 66841-25-6
- CAS-Number
- C22H19Br4NO3
- Molecular Formula
- 665.01
- Molecular Weight
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
- Shipping
- AMBIENT
- Short Term Storage
- RT
- Long Term Storage
- +4°C
- Handling Advice
- Protect from light and moisture.
- Use / Stability
- Stable for at least 2 years after receipt when stored at +4°C.
- Hazard statements
- H302-H315-H319-H410
- Precautionary statements
- P273-P305 + P351 + P338-P501
- GHS Symbol
- GHS07+GHS09
- Signal word
- Warning
- RIDADR
- UN3077 9
- Transportation
- Packing Group III
- Description
- Potent pyrethroid insecticide. Mode of action is by modifying the gating kinetics of the sodium channels in neurons, increasing the length of time the channel remains open after a stimulus, thereby depolarizing the neuron for a longer period of time. This leads to uncontrolled spasming, paralysis and eventual death. It is effective against most members of class Arachnida as well as insects.
- Smiles
- O=C([C@H]1C(C)(C)[C@H]1C(Br)C(Br)(Br)Br)O[C@H](C#N)C2=CC=CC(OC3=CC=CC=C3)=C2
- InChi Key
- YWSCPYYRJXKUDB-KAKFPZCNSA-N
- References
- B. Hue & L. Mony, Comp. Biochem. Physiol. C 86, 349 (1987) , L.D. Brown & T. Narahashi, Toxicol. Appl. Pharmacol. 89, 305 (1987) , D.D. Amalraj, et al., Indian J. Malariol. 28, 141 (1991) , D.A. Laskowski, Review Env. Conat≥ Toxic. 174, 49 (2002)
- InChi
- InChI=1S/C22H19Br4NO3/c1-21(2)17(19(23)22(24,25)26)18(21)20(28)30-16(12-27)13-7-6-10-15(11-13)29-14-8-4-3-5-9-14/h3-11,16-19H,1-2H3/t16-,17-,18+,19?/m1/s1
Potent pyrethroid insecticide. Mode of action is by modifying the gating kinetics of the sodium channels in neurons, increasing the length of time the channel remains open after a stimulus, thereby depolarizing the neuron for a longer period of time. This leads to uncontrolled spasming, paralysis and eventual death. It is effective against most members of class Arachnida as well as insects.
Additional information
| Synonyms | (S)-α-Cyano-3-phenoxybenzyl (1R,3S)-2,2-dimethyl-3-[(RS)-1,2,2,2-tetrabromoethyl]cyclopropanecarboxylate |
|---|---|
| Purity | ≥98% (HPLC) |
| Appearance | Off-white solid |
| CAS-Number | 66841-25-6 |
| Molecular Formula | C22H19Br4NO3 |
| Molecular Weight | 665.01 |
| Identity | 1H-NMR |
| Solvents | acetone, toluene, ethanol, water (practically insoluble) |
| Melting Point | 138-148°C |
| Density | 1.70 g/cm3 at 20°C |
| Smiles | O=C([C@H]1C(C)(C)[C@H]1C(Br)C(Br)(Br)Br)O[C@H](C#N)C2=CC=CC(OC3=CC=CC=C3)=C2 |
| InChi Key | YWSCPYYRJXKUDB-KAKFPZCNSA-N |
| Shipping | AMBIENT |
| Short Term Storage | RT |
| Long Term Storage | +4°C |
| Handling Advice | Protect from light and moisture. |
| Use / Stability | Stable for at least 2 years after receipt when stored at +4°C. |
| Hazard statements | H302-H315-H319-H410 |
| Precautionary statements | P273-P305 + P351 + P338-P501 |
| GHS Symbol | GHS07+GHS09 |
| Signal word | Warning |
| RIDADR | UN3077 9 |
| Transportation | Packing Group III |
| References | B. Hue & L. Mony, Comp. Biochem. Physiol. C 86, 349 (1987), L.D. Brown & T. Narahashi, Toxicol. Appl. Pharmacol. 89, 305 (1987), D.D. Amalraj, et al., Indian J. Malariol. 28, 141 (1991), D.A. Laskowski, Review Env. Conat≥ Toxic. 174, 49 (2002) |
| InChi | InChI=1S/C22H19Br4NO3/c1-21(2)17(19(23)22(24,25)26)18(21)20(28)30-16(12-27)13-7-6-10-15(11-13)29-14-8-4-3-5-9-14/h3-11,16-19H,1-2H3/t16-,17-,18+,19?/m1/s1 |
| Quantity | 100 mg, 500 mg, Bulk |
