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主要文件

COO原产地证书/COA分析证书

PHR2279

Lovastatin Impurity D

Name: Lovastatin Impurity D
Brand: SIAL

Pharmaceutical Secondary Standard; Certified Reference Material

别名:

[(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

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About This Item

经验公式（希尔记法）:

C₄₈H₇₂O₁₀

CAS号:

149756-62-7

分子量:

809.08

UNSPSC代码:

41116107

NACRES:

NA.24

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Lovastatin Related Compound A

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Multiscreen^® 96 well Plate, hydrophilic PVDF membrane

PHL80307

红曲素K

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棒曲霉素溶液溶液

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Y0001721

罗伐他汀钙盐

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1344666

Iohexol Related Compound C

USP

1708773

Valsartan Related Compound A

Z183423

Foil/poly bag

等级

certified reference material
pharmaceutical secondary standard

质量水平

300

API类

lovastatin

表单

powder

包装

pkg of 20 mg

应用

pharmaceutical

储存温度

-10 to -25°C

SMILES字符串

O1C(C[C@H](CC1=O)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H]4[C@H]5[C@H](C[C@H](C=C5C=C[C@@H]4C)C)OC(=O)[C@H](CC)C)CC[C@@H]2[C@H]3[C@H](C[C@H](C=C3C=C[C@@H]2C)C)OC(=O)[C@H](CC)C

InChI

1S/C48H72O10/c1-9-29(5)47(53)57-41-21-27(3)19-33-13-11-31(7)39(45(33)41)17-15-35(49)23-36(50)24-43(51)56-38-25-37(55-44(52)26-38)16-18-40-32(8)12-14-34-20-28(4)22-42(46(34)40)58-48(54)30(6)10-2/h11-14,19-20,27-32,35-42,45-46,49-50H,9-10,15-18,21-26H2,1-8H3/t27-,28-,29-,30-,31-,32-,35+,36+,37?,38+,39-,40-,41-,42-,45-,46-/m0/s1

InChI key

GZGUDHDMNATZDU-CRMSOXFQSA-N

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

应用

These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

分析说明

These secondary standards offer multi-traceability to the USP, EP and BP primary standards, where they are available.

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.

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.

象形图

GHS08

警示用语：

Warning

危险声明

H351,H361f,H413

预防措施声明

P201 - P273 - P308 + P313

危险分类

Aquatic Chronic 4 - Carc. 2 - Repr. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 3

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主要文件

Lovastatin Impurity D

Pharmaceutical Secondary Standard; Certified Reference Material

About This Item

推荐产品

属性

等级

质量水平

API类

表单

包装

应用

储存温度

SMILES字符串

InChI

InChI key

相关类别

说明

一般描述

应用

分析说明

其他说明

附注

相关产品

相关产品

安全信息

象形图

警示用语：

危险声明

预防措施声明

危险分类

储存分类代码

WGK

文件

分析证书(COA)

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