- Pyributicarb
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- $63.00 / 50mg
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2026-04-22
- CAS:88678-67-5
- Min. Order:
- Purity: 99.70%
- Supply Ability: 10g
- Pyributicarb
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- $1.00 / 1KG
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2020-02-14
- CAS:88678-67-5
- Min. Order: 1KG
- Purity: Min98% HPLC
- Supply Ability: G/KG/TON
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| | Pyributicarb Basic information |
| Product Name: | Pyributicarb | | Synonyms: | carbamothioicacid,(6-methoxy-2-pyridinyl)methyl-,o-(3-(1,1-dimethylethyl)p;henyl)ester;n-(6-methoxy-2-pyridyl)-n-methyl-thiocarbamicacio-3-tert-butylphenyleste;tsh-888;PYRIBUTICARB;PYRIBUTYCARB;n-(6-methoxy-2-pyridyl)-n-methylthiocarbamic acid o-3-tert-butylphenyl ester;O-3-tert-Butylphenyl (6-methoxy-2-pyridyl)(methyl)thiocarbamate | | CAS: | 88678-67-5 | | MF: | C18H22N2O2S | | MW: | 330.44 | | EINECS: | | | Product Categories: | | | Mol File: | 88678-67-5.mol |  |
| | Pyributicarb Chemical Properties |
| Melting point | 85～88℃ | | Boiling point | 427.8±55.0 °C(Predicted) | | density | 1.1453 (rough estimate) | | refractive index | 1.6000 (estimate) | | storage temp. | 0-6°C | | solubility | DMSO : 100 mg/mL (302.63 mM);Water : < 0.1 mg/mL (insoluble) | | form | Solid | | pka | 1.22±0.10(Predicted) | | color | White to off-white | | Henry's Law Constant | 4.3×101 mol/(m3Pa) at 25℃, Ebert et al. (2023) | | InChI | InChI=1S/C18H22N2O2S/c1-18(2,3)13-8-6-9-14(12-13)22-17(23)20(4)15-10-7-11-16(19-15)21-5/h6-12H,1-5H3 | | InChIKey | VTRWMTJQBQJKQH-UHFFFAOYSA-N | | SMILES | C(=S)(OC1=CC=CC(C(C)(C)C)=C1)N(C1=NC(OC)=CC=C1)C |
| Hazard Codes | N | | Risk Statements | 50/53 | | Safety Statements | 61 | | RIDADR | UN 3077 9 / PGIII | | WGK Germany | 3 | | RTECS | XK4962000 | | HS Code | 29333990 |
| | Pyributicarb Usage And Synthesis |
| Chemical Properties | Barnyard Fear is a white crystalline solid, melting point 85.7 ~ 86.2 ℃, vapor pressure 0.0119mPa (40 ℃), relative density of 1.20 (20 ℃), solubility in water 0.15mg / L (20 ℃), organic solvents in the solubility (20 ℃, g / L): acetone 454, methanol 21, ethanol 33, xylene 355, ethyl acetate 384. 273 ℃ are stable. Stable below 273℃. | | Uses | Pyributicarb, is a carbamate-type herbicide, acting as a potent activator of both CYP3A4 gene and human pregnane X receptor (hPXR). | | Definition | ChEBI: A monothiocarbamic ester that is carbamic acid in which the oxygen of the oxo group is replaced by sulfur, the hydrogens attached to the nitrogen are replaced by methyl and 6-methoxypyridin-2-yl groups, and the hydrogen of the hydroxy group is replaced by
p-tert-butylphenyl group. It has fungicidal and herbicidal activity and is used in paddy rice and turf production. | | in vivo | Pyributicarb causes enhancement of CYP3A4-derived reporter activity in mouse livers introduced with hPXR by adenovirus[1]. |
| | Pyributicarb Preparation Products And Raw materials |
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