| Identification | Back Directory | [Name]
PROSULFOCARB | [CAS]
52888-80-9 | [Synonyms]
DEFI
BOXER
arkade
r15574
PROSULFOCARB
prosulfocarb (bsi,iso)
boxer(iciagrochemicals)
benzyldipropylthiolcarbamate
S-BENZYL DIPROPYLTHIOCARBAMATE
s-benzyldipropylthiolcarbamate
S-BENZYL N,N-DIPROPYLTHIOCARBAMATE)
dipropylthio-carbamicacis-benzylester
s-(phenylmethyl)dipropylcarbamothioate
PROSULFOCARB PESTANAL (S-BENZYLDI-PROPY
dipropyl-carbamothioicacis-(phenylmethyl)ester
S-benzyl N,N-dipropylthiocarbamate prosulfocarb
Carbamothioic acid, dipropyl-, S-(phenylmethyl) ester | [EINECS(EC#)]
401-730-6 | [Molecular Formula]
C14H21NOS | [MDL Number]
MFCD00145179 | [MOL File]
52888-80-9.mol | [Molecular Weight]
251.39 |
| Chemical Properties | Back Directory | [Melting point ]
25°C | [Boiling point ]
129 °C | [density ]
1.0696 (rough estimate) | [refractive index ]
1.7500 (estimate) | [Fp ]
100 °C | [storage temp. ]
2-8°C | [form ]
neat | [pka]
-1.22±0.70(Predicted) | [BRN ]
4804364 | [Henry's Law Constant]
7.6×102 mol/(m3Pa) at 25℃, Duchowicz et al. (2020) | [Major Application]
agriculture
environmental | [InChI]
1S/C14H21NOS/c1-3-10-15(11-4-2)14(16)17-12-13-8-6-5-7-9-13/h5-9H,3-4,10-12H2,1-2H3 | [InChIKey]
NQLVQOSNDJXLKG-UHFFFAOYSA-N | [SMILES]
CCCN(CCC)C(=O)SCc1ccccc1 | [LogP]
4.650 | [EPA Substance Registry System]
Prosulfocarb (52888-80-9) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn,N | [Risk Statements ]
22-43-51/53 | [Safety Statements ]
24-37-61 | [RIDADR ]
UN 3082 9/PG 3 | [WGK Germany ]
2 | [RTECS ]
FD3835000 | [REACH Registrations]
Inactive | [HS Code ]
29302000 | [Storage Class]
10 - Combustible liquids | [Hazard Classifications]
Acute Tox. 4 Oral
Aquatic Chronic 2
Skin Sens. 1 |
| Hazard Information | Back Directory | [Air & Water Reactions]
Thio and dithiocarbamates slowly decompose in aqueous solution to form carbon disulfide and methylamine or other amines. Such decompositions are accelerated by acids. | [Reactivity Profile]
PROSULFOCARB is a thiocarbamate. Flammable gases are generated by the combination of thiocarbamates and dithiocarbamates with aldehydes, nitrides, and hydrides. Thiocarbamates and dithiocarbamates are incompatible with acids, peroxides, and acid halides. | [Uses]
Prosulfocarb is a pesticide used in the protection of crops such as barley for its herbicidal activity. | [Definition]
ChEBI: A monothiocarbamic ester that is carbamothioic S-acid substituted by two propyl groups at the nitrogen atom and a benzyl group at the the sulfur atom. | [Production Methods]
Prosulfocarb is commercially produced via a two-step process starting from diisopropylamine, which is reacted with carbon disulphide in the presence of sodium hydroxide in aqueous or toluene medium at to form sodium diisopropylcarbamodithioate. This intermediate is then alkylated with benzyl chloride in a phase-transfer catalysed system, yielding prosulfocarb. | [Synthesis Reference(s)]
Tetrahedron, 49, p. 2403, 1993 DOI: 10.1016/S0040-4020(01)86319-5 | [Mechanism of action]
Selective, absorbed by leaves and roots. Lipid synthesis inhibitor. | [Pesticide Type]
Herbicide |
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| Company Name: |
Spectrum Chemical Manufacturing Corp.
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| Tel: |
021-021-021-67601398-809-809-809 15221380277 |
| Website: |
www.spectrumchemical.com/oa_html/index.jsp?minisite=10020&respid=22372&language=us |
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