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Lovastatin Impurity D
| 产品编号： | 4119938 |
| 规格： | Pharmaceutical Secondary Standard; Certified Reference Material |
| CAS NO： | 149756-62-7 |
| 包装规格： | 20 mg |
| 产品类别： | 进口试剂 |
| 品牌： | Supelco |
| 优惠价： | 立即咨询 |
产品别名
149756-62-7
Lovastatin Impurity D
[(4R)-2-[2-[(1S,2S,6R,8S,8aR)-2,6-Dimethyl-8-[(2S)-2-methylbutanoyl]oxy-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl]-6-oxooxan-4-yl] (3R,5R)-7-[(1S,2S,6R,8S,8aR)-2,6-dimethyl-8-[(2S)-2-methylbutanoyl]oxy-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoate
基本信息
| Empirical Formula【经验(实验)分子式】 | C48H72O10 |
| Molecular weight | 809.08 |
| General description【一般描述】 | Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards |
| Analysis Note【分析说明】 | These secondary standards offer multi-traceability to the USP, EP and BP primary standards, where they are available. |
| Other Notes【其他说明】 | This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis. |
| Footnote【附注】 | To see an example of a Certificate of Analysis for this material enter LRAC3719 in the Documents slot below. This is an example certificate only and may not be the lot that you receive. |
产品性质
| grade【等级】 | certified reference material pharmaceutical secondary standard |
| form【形式】 | powder |
| packaging【包装】 | pkg of 20 mg |
| storage temp.【储存温度】 | -10 to -25℃ |
安全信息
| Pictograms【象形图】 | GHS08 |
| Signal word【警示用语：】 | Warning |
| Hazard Statements | H351 - H361f - H413 |
| Precautionary Statements | P201 - P273 - P308 + P313 |
| Hazard Classifications【危险分类】 | Aquatic Chronic 4 - Carc. 2 - Repr. 2 |
| Storage Class Code【储存分类代码】 | 11 - Combustible Solids |
| WGK | WGK 3 |
