BUTAMIFOS
- Product Name
- BUTAMIFOS
- CAS No.
- 36335-67-8
- Chemical Name
- BUTAMIFOS
- Synonyms
- s28;s2846;h26905;tufler;kremart;CREMART;Cremarat;BUTAMIFOS;metacrefos;hercules26905
- CBNumber
- CB6152868
- Molecular Formula
- C13H21N2O4PS
- Formula Weight
- 332.36
- MOL File
- 36335-67-8.mol
BUTAMIFOS Property
- Melting point:
- <25 °C
- Boiling point:
- 422.1±55.0 °C(Predicted)
- Density
- 1.223±0.06 g/cm3(Predicted)
- storage temp.
- 0-6°C
- pka
- -0.51±0.70(Predicted)
- BRN
- 2165895
- EPA Substance Registry System
- Phosphoramidothioic acid, (1-methylpropyl)-, O-ethyl O-(5-methyl-2-nitrophenyl) ester (36335-67-8)
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H410Very toxic to aquatic life with long lasting effects
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P273Avoid release to the environment.
P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P391Collect spillage. Hazardous to the aquatic environment
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- 37046
- Product name
- Butamifos
- Purity
- PESTANAL
- Packaging
- 25mg
- Price
- $128
- Updated
- 2022/05/15
- Product number
- 1553BA
- Product name
- Butamifos
- Packaging
- 25mg
- Price
- $320
- Updated
- 2021/12/16
- Product number
- CHM0165659
- Product name
- BUTAMIFOS
- Purity
- 98.00%
- Packaging
- 10MG
- Price
- $750.75
- Updated
- 2021/12/16
- Product number
- CHM0165659
- Product name
- BUTAMIFOS
- Purity
- 98.00%
- Packaging
- 100MG
- Price
- $1963.5
- Updated
- 2021/12/16
- Product number
- CHM0165659
- Product name
- BUTAMIFOS
- Purity
- 98.00%
- Packaging
- 50ML
- Price
- $2695
- Updated
- 2021/12/16
BUTAMIFOS Chemical Properties,Usage,Production
Definition
ChEBI: Butamifos is a C-nitro compound.
Metabolic pathway
In water, butamifos undergoes photoinduced intramolecular oxygen transfer from the nitro group to the P=?S moiety, resulting in the formation of the nitrosooxon derivative. Through the successive reduction of the nitroso group to hydroxyamino and amino groups, as well as oxidation to the nitro group, the nitrosooxon derivative is finally photodegraded to various polar compounds. The isomer of butamifos is photodegraded more slowly than butamifos in air, and its main photodegradation pathway in water is oxidation of the arylmethyl group to form a corresponding carboxylic acid derivative.