Name | thiacloprid |
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Synonyms |
(3-((6-chloro-3-pyridinyl)methyl)-2-thiazolidinylidene)cyanamide
Cyanamide, N-[(2E)-3-[(6-chloro-3-pyridinyl)methyl]-2-thiazolidinylidene]- {(2E)-3-[(6-Chloro-3-pyridinyl)methyl]-1,3-thiazolidin-2-ylidene}cyanamide Cyanamide, (3-((6-chloro-3-pyridinyl)methyl)-2-thiazolidinylidene)- (Z)-3-(6-chloro-3-pyridylmethyl)-1,3-thiazolidin-2-ylidenecyanamide {(2Z)-3-[(6-chloropyridin-3-yl)methyl]-1,3-thiazolidin-2-ylidene}cyanamide [3-[(6-chloropyridin-3-yl)methyl]-1,3-thiazolidin-2-ylidene]cyanamide (Z)-[3-[(6-chloro-3-pyridinyl)methyl]-2-thiazolidinylidene]cyanamide {(2E)-3-[(6-chloropyridin-3-yl)methyl]-1,3-thiazolidin-2-ylidene}cyanamide Thiacloprid MFCD02101042 |
Description | Thiacloprid, a chloronicotinyl insecticide, is targeted chiefly to control aphid pest species in orchards and vegetables[1]. Thiacloprid destabilizes DNA. Thiacloprid changes the structure and stability of DNA through binding into the minor groove by hydrophobic or hydrogen interactions[2]. |
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Related Catalog | |
References |
Density | 1.4±0.1 g/cm3 |
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Boiling Point | 423.1±55.0 °C at 760 mmHg |
Melting Point | 136ºC |
Molecular Formula | C10H9ClN4S |
Molecular Weight | 252.723 |
Flash Point | 209.7±31.5 °C |
Exact Mass | 252.023651 |
PSA | 77.58000 |
LogP | 0.55 |
Vapour Pressure | 0.0±1.0 mmHg at 25°C |
Index of Refraction | 1.691 |
Storage condition | 0-6°C |
Symbol |
GHS06, GHS08, GHS09 |
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Signal Word | Danger |
Hazard Statements | H301-H332-H336-H351-H360FD-H410 |
Precautionary Statements | Missing Phrase - N15.00950417-P201-P261-P280-P308 + P313 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Faceshields;Gloves |
Hazard Codes | Xn |
Risk Phrases | R20/22 |
Safety Phrases | S60 |
RIDADR | 2588 |
RTECS | GS6093749 |
Packaging Group | III |
Hazard Class | 6.1(b) |