| 规格 | 价格 | |
|---|---|---|
| 500mg | ||
| 1g | ||
| Other Sizes |
| 药代性质 (ADME/PK) |
Absorption, Distribution and Excretion
Absorbed through the leaves from surface treatment, but the major significant route for uptake is via root system. ... Uptake through the roots is best described as osmotic diffusion. Metribuzin is translocated upward in the xylem and moves distally when applied at the base of leaves. After absorption, it is rapidly distributed and rapidly excreted unchangd or metabolized (oxidized) and excreted via the urine. Metabolism / Metabolites When (14)C metribuzin was applied to tomatoes, preliminary evidence indicated that the first (14)C metabolite may be a complex with deaminated diketometribuzin or metribuzin. Metribuzin applied to roots of soybean (Glycine max (Leguminatae) Merr. 'Cutler') seedlings was rapidly absorbed and translocated to the shoots. The major product observed was deaminated metribuzin. The 3,5-diketo and deaminated diketo derivatives were also observed. Identity of these metabolites was determined by cochromatography and MS. Roots and shoots both produced these compounds. The aglycones of four acid labile carbohydrate conjugates formed were identified as 3,5-diketo derivative and deaminated derivative. Potatoes were planted in soil treated with metribuzin. Analyses of plant material showed the presence of metribuzin, 3,5-diketo and deaminated derivative as well as conjugated material. Analyses indicated that deaminated diketo was the aglycone of one conjugate. When these studies were repeated in the same soil, another metabolite was found in the top part of the plants and identified as trimethylpyruvic acid semicarbazone. Similar results were observed with carrots and the soil in which these plants had been grown. |
|---|---|
| 毒性/毒理 (Toxicokinetics/TK) |
Non-Human Toxicity Values
LD50 Rat oral 1100 mg/kg LD50 Rat dermal >2000 mg/kg LD50 Rabbit dermal >2000 mg/kg LD50 Mouse oral 698-711 mg/kg For more Non-Human Toxicity Values (Complete) data for METRIBUZIN (16 total), please visit the HSDB record page. |
| 其他信息 |
Metribuzin is a colorless crystalline solid. Used as an herbicide. (NIOSH, 2024)
Metribuzin is a member of the class of 1,2,4-triazines that is 1,2,4-triazin-5(4H)-one substituted by an amino group at position 4, tert-butyl group at position 6 and a methylsulfanyl group at position 3. It has a role as a xenobiotic, an environmental contaminant, a herbicide and an agrochemical. It is a member of 1,2,4-triazines, an organic sulfide and a cyclic ketone. Metribuzin (4-amino-6-tert-butyl-3-(methylthio)-as-triazin-5 (4H)-one) is a herbicide used both pre- and post-emergence in crops including soy bean, potatoes, tomatoes and sugar cane. It acts by inhibiting photosynthesis by disrupting photosystem II. It is widely used in agriculture and has been found to contaminate groundwater. Mechanism of Action Inhibits photosynthesis |
| 分子式 |
C8H14N4OS
|
|---|---|
| 精确质量 |
214.088
|
| CAS号 |
21087-64-9
|
| PubChem CID |
30479
|
| 外观&性状 |
Colorless crytals
White crystalline solid |
| 密度 |
1.3±0.1 g/cm3
|
| 沸点 |
312.4±25.0 °C at 760 mmHg
|
| 熔点 |
125°C
|
| 闪点 |
142.7±23.2 °C
|
| 蒸汽压 |
0.0±0.7 mmHg at 25°C
|
| 折射率 |
1.618
|
| LogP |
1.3
|
| tPSA |
99.1
|
| 氢键供体(HBD)数目 |
1
|
| 氢键受体(HBA)数目 |
5
|
| 可旋转键数目(RBC) |
2
|
| 重原子数目 |
14
|
| 分子复杂度/Complexity |
316
|
| 定义原子立体中心数目 |
0
|
| SMILES |
O=C1N(C(SC)=NN=C1C(C)(C)C)N
|
| InChi Key |
FOXFZRUHNHCZPX-UHFFFAOYSA-N
|
| InChi Code |
InChI=1S/C8H14N4OS/c1-8(2,3)5-6(13)12(9)7(14-4)11-10-5/h9H2,1-4H3
|
| 化学名 |
4-amino-6-tert-butyl-3-methylsulfanyl-1,2,4-triazin-5-one
|
| 别名 |
Metribuzin DIC 1468 Sencor
|
| HS Tariff Code |
2934.99.9001
|
| 存储方式 |
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
| 运输条件 |
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
|
| 溶解度 (体外实验) |
May dissolve in DMSO (in most cases), if not, try other solvents such as H2O, Ethanol, or DMF with a minute amount of products to avoid loss of samples
|
|---|---|
| 溶解度 (体内实验) |
注意: 如下所列的是一些常用的体内动物实验溶解配方,主要用于溶解难溶或不溶于水的产品(水溶度<1 mg/mL)。 建议您先取少量样品进行尝试,如该配方可行,再根据实验需求增加样品量。
注射用配方
注射用配方1: DMSO : Tween 80: Saline = 10 : 5 : 85 (如: 100 μL DMSO → 50 μL Tween 80 → 850 μL Saline)(IP/IV/IM/SC等) *生理盐水/Saline的制备:将0.9g氯化钠/NaCl溶解在100 mL ddH ₂ O中,得到澄清溶液。 注射用配方 2: DMSO : PEG300 :Tween 80 : Saline = 10 : 40 : 5 : 45 (如: 100 μL DMSO → 400 μL PEG300 → 50 μL Tween 80 → 450 μL Saline) 注射用配方 3: DMSO : Corn oil = 10 : 90 (如: 100 μL DMSO → 900 μL Corn oil) 示例: 以注射用配方 3 (DMSO : Corn oil = 10 : 90) 为例说明, 如果要配制 1 mL 2.5 mg/mL的工作液, 您可以取 100 μL 25 mg/mL 澄清的 DMSO 储备液,加到 900 μL Corn oil/玉米油中, 混合均匀。 View More
注射用配方 4: DMSO : 20% SBE-β-CD in Saline = 10 : 90 [如:100 μL DMSO → 900 μL (20% SBE-β-CD in Saline)] 口服配方
口服配方 1: 悬浮于0.5% CMC Na (羧甲基纤维素钠) 口服配方 2: 悬浮于0.5% Carboxymethyl cellulose (羧甲基纤维素) 示例: 以口服配方 1 (悬浮于 0.5% CMC Na)为例说明, 如果要配制 100 mL 2.5 mg/mL 的工作液, 您可以先取0.5g CMC Na并将其溶解于100mL ddH2O中,得到0.5%CMC-Na澄清溶液;然后将250 mg待测化合物加到100 mL前述 0.5%CMC Na溶液中,得到悬浮液。 View More
口服配方 3: 溶解于 PEG400 (聚乙二醇400) 请根据您的实验动物和给药方式选择适当的溶解配方/方案: 1、请先配制澄清的储备液(如:用DMSO配置50 或 100 mg/mL母液(储备液)); 2、取适量母液,按从左到右的顺序依次添加助溶剂,澄清后再加入下一助溶剂。以 下列配方为例说明 (注意此配方只用于说明,并不一定代表此产品 的实际溶解配方): 10% DMSO → 40% PEG300 → 5% Tween-80 → 45% ddH2O (或 saline); 假设最终工作液的体积为 1 mL, 浓度为5 mg/mL: 取 100 μL 50 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀/澄清;向上述体系中加入50 μL Tween-80,混合均匀/澄清;然后继续加入450 μL ddH2O (或 saline)定容至 1 mL; 3、溶剂前显示的百分比是指该溶剂在最终溶液/工作液中的体积所占比例; 4、 如产品在配制过程中出现沉淀/析出,可通过加热(≤50℃)或超声的方式助溶; 5、为保证最佳实验结果,工作液请现配现用! 6、如不确定怎么将母液配置成体内动物实验的工作液,请查看说明书或联系我们; 7、 以上所有助溶剂都可在 Invivochem.cn网站购买。 |
计算结果:
工作液浓度: mg/mL;
DMSO母液配制方法: mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL)。如该浓度超过该批次药物DMSO溶解度,请首先与我们联系。
体内配方配制方法:取 μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL ddH2O,混匀澄清。
(1) 请确保溶液澄清之后,再加入下一种溶剂 (助溶剂) 。可利用涡旋、超声或水浴加热等方法助溶;
(2) 一定要按顺序加入溶剂 (助溶剂) 。