| Company Name: |
Sigma-Aldrich
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| Tel: |
021-61415566 800-8193336 |
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orderCN@merckgroup.com |
| Products Intro: |
Product Name:Triadimenol A
CAS:70585-35-2
Purity:PESTANAL(R), analytical standard Package:250MG Remarks:45694-250MG
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| Company Name: |
Alta Scientific Co., Ltd.
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| Tel: |
022-6537-8550 15522853686 |
| Email: |
sales@altasci.com.cn |
| Products Intro: |
Product Name:Triadimenol A
CAS:70585-35-2
Purity:99% Package:10mg,100mg
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| Company Name: |
TCI (Shanghai) Chemical Trading Co., Ltd.
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| Tel: |
021-61109150 |
| Email: |
sales@tcisct.com |
| Products Intro: |
Product Name:Triadimenol isomer A
CAS:70585-35-2
Package:1KG;10KG;100KG; Remarks: 纯度：根据客户需求提供
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| Company Name: |
guoyungurui
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| Tel: |
18162595016 |
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3287908757@qq.com |
| Products Intro: |
Product Name:*Aminocarb
CAS:70585-35-2
Purity:95%+HPLC Package:10mg;25mg;50mg;100mg;200mg
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| Company Name: |
Riedel-de Haen AG
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| Tel: |
800 558-9160 |
| Email: |
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| Products Intro: |
Product Name:Triadimenol A
CAS:70585-35-2
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| | (aR,)-rel-a-tert-Butyl-b-(4-chlorophenoxy)-1H-1,2,4-triazole-1-ethanol PESTANAL Basic information |
| Product Name: | (aR,)-rel-a-tert-Butyl-b-(4-chlorophenoxy)-1H-1,2,4-triazole-1-ethanol PESTANAL | | Synonyms: | (αR,βS)-rel-α-tert-Butyl-β-(4-chlorophenoxy)-1H-1,2,4-triazole-1-ethanol;(aR,)-rel-a-tert-Butyl-b-(4-chlorophenoxy)-1H-1,2,4-triazole-1-ethanol PESTANAL;1H-1,2,4-Triazole-1-ethanol, β-(4-chlorophenoxy)-α-(1,1-dimethylethyl)-, (αR,βS)-rel- | | CAS: | 70585-35-2 | | MF: | C14H18ClN3O2 | | MW: | 295.76 | | EINECS: | | | Product Categories: | | | Mol File: | 70585-35-2.mol |  |
| | (aR,)-rel-a-tert-Butyl-b-(4-chlorophenoxy)-1H-1,2,4-triazole-1-ethanol PESTANAL Chemical Properties |
| Boiling point | 465.4±55.0 °C(Predicted) | | density | 1.24±0.1 g/cm3(Predicted) | | Fp | 100 °C | | pka | 13.29±0.20(Predicted) |
| Hazard Codes | Xn | | Risk Statements | 22-52/53 | | Safety Statements | 61 | | WGK Germany | 2 |
| | (aR,)-rel-a-tert-Butyl-b-(4-chlorophenoxy)-1H-1,2,4-triazole-1-ethanol PESTANAL Usage And Synthesis |
| Uses | Triadimenol A is a fungicide and is formed through the enantioselective degradation, abiotic racemization, and chiral transformation of triadimefon in soils. |
| | (aR,)-rel-a-tert-Butyl-b-(4-chlorophenoxy)-1H-1,2,4-triazole-1-ethanol PESTANAL Preparation Products And Raw materials |
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