Specifications
- Purity
- ≥97% (NMR)
- Appearance
- Buff or brown liquid
- Identity
- 1H-NMR
Properties
- Solvents
- chloroform, ethyl acetate, acetone, ethanol, methanol, water (insoluble)
Available from stock
Prosulfocarb
- SKU
- P0187
Category: Herbicides
- Synonyms
- S-Benzyl dipropylthiocarbamate , BRN 4804364
- 52888-80-9
- CAS-Number
- C14H21NOS
- Molecular Formula
- 251.39
- Molecular Weight
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
- Shipping
- AMBIENT
- Short Term Storage
- +4°C
- Long Term Storage
- -20°C
- Handling Advice
- Protect from light and moisture.
- Use / Stability
- Stable for at least 2 years after receipt when stored at -20°C.
- Hazard statements
- H302, H317, H411
- Precautionary statements
- P273, P280
- GHS Symbol
- GHS07+GHS09
- Signal word
- Warning
- RIDADR
- UN3082 / 9
- Transportation
- Packing Group III
- Description
- Thiocarbamate herbicide. Targets the meristematic region, or growing points, of plants – on both roots and shoots. Mode of action is through inhibition of lipid synthesis in plant cells. In particular, it inhibits fatty acid elongase enzymes, altering cell membranes and disrupting vital cell processes. It also effects the development of cutin and suberin, two waxy polymers that help to form plant cuticles. The result is that meristems are inhibited, root and shoot development is stunted, new leaves fail to emerge and shoots twist and turn dark green. Used for post-emergence control of grass and broad-leaved weeds in a wide range of crops. Compound can be used as analytical reference material.
- Smiles
- O=C(SCC1=CC=CC=C1)N(CCC)CCC
- InChi Key
- NQLVQOSNDJXLKG-UHFFFAOYSA-N
- References
- (1) D.Callens & R. Bulcke , Meded. Fac. Landbouwwet, Univ. Gent 60, 141 (1995) , (2) The Pesticide Manual, 11th Edition: C. Tomlin , British Crop Protection Council (1997) , (3) M. Gennari, et al. , J. Environ. Sci. Health B 37, 297 (2002)
Thiocarbamate herbicide. Targets the meristematic region, or growing points, of plants – on both roots and shoots. Mode of action is through inhibition of lipid synthesis in plant cells. In particular, it inhibits fatty acid elongase enzymes, altering cell membranes and disrupting vital cell processes. It also effects the development of cutin and suberin, two waxy polymers that help to form plant cuticles. The result is that meristems are inhibited, root and shoot development is stunted, new leaves fail to emerge and shoots twist and turn dark green. Used for post-emergence control of grass and broad-leaved weeds in a wide range of crops. Compound can be used as analytical reference material.
Additional information
| Synonyms | S-Benzyl dipropylthiocarbamate, BRN 4804364 |
|---|---|
| Purity | ≥97% (NMR) |
| Appearance | Buff or brown liquid |
| CAS-Number | 52888-80-9 |
| Molecular Formula | C14H21NOS |
| Molecular Weight | 251.39 |
| Identity | 1H-NMR |
| Solvents | chloroform, ethyl acetate, acetone, ethanol, methanol, water (insoluble) |
| Smiles | O=C(SCC1=CC=CC=C1)N(CCC)CCC |
| InChi Key | NQLVQOSNDJXLKG-UHFFFAOYSA-N |
| Shipping | AMBIENT |
| Short Term Storage | +4°C |
| Long Term Storage | -20°C |
| Handling Advice | Protect from light and moisture. |
| Use / Stability | Stable for at least 2 years after receipt when stored at -20°C. |
| Hazard statements | H302, H317, H411 |
| Precautionary statements | P273, P280 |
| GHS Symbol | GHS07+GHS09 |
| Signal word | Warning |
| RIDADR | UN3082 / 9 |
| Transportation | Packing Group III |
| References | (1) D.Callens & R. Bulcke, Meded. Fac. Landbouwwet, Univ. Gent 60, 141 (1995), (2) The Pesticide Manual, 11th Edition: C. Tomlin, British Crop Protection Council (1997), (3) M. Gennari, et al., J. Environ. Sci. Health B 37, 297 (2002) |
| Quantity | 500 mg, 1 g, Bulk |
