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Merck

94664

Supelco

無水テトラサイクリン 塩酸塩

certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

別名:

(4S,4aS,12aS)-4-(ジメチルアミノ)-1,4,4a,5,12,12a-ヘキサヒドロ-3,10,11,12a-テトラヒドロキシ-6-メチル-1,12-ジオキソ-2-ナフタセンカルボキサミド 一塩酸塩

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About This Item

実験式(ヒル表記法):
C22H22N2O7 · HCl
CAS番号:
分子量:
462.88
Beilstein:
4228856
MDL番号:
UNSPSCコード:
41116107
PubChem Substance ID:
NACRES:
NA.24

グレード

certified reference material
TraceCERT®

品質水準

製品種目

TraceCERT®

シェルフライフ

limited shelf life, expiry date on the label

メーカー/製品名

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

保管条件

under inert gas (argon)

テクニック

HPLC: suitable
gas chromatography (GC): suitable

アプリケーション

forensics and toxicology
pharmaceutical (small molecule)

フォーマット

neat

輸送温度

wet ice

保管温度

−20°C

SMILES記法

Cl[H].[H][C@@]12Cc3c(C)c4cccc(O)c4c(O)c3C(=O)[C@]1(O)C(=O)C(C(N)=O)=C(O)[C@H]2N(C)C

InChI

1S/C22H22N2O7.ClH/c1-8-9-5-4-6-12(25)13(9)17(26)14-10(8)7-11-16(24(2)3)18(27)15(21(23)30)20(29)22(11,31)19(14)28;/h4-6,11,16,25-27,31H,7H2,1-3H3,(H2,23,30);1H/t11-,16-,22-;/m0./s1

InChI Key

XBSQEFHDCDFNJU-WPJNXPDPSA-N

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詳細

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com.

アプリケーション

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

包装

底の開いたガラス瓶内容物は内部に挿入され接着された円錐部に入っています。

法的情報

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany

保管分類コード

11 - Combustible Solids

WGK

WGK 3

引火点(°F)

Not applicable

引火点(℃)

Not applicable


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Today's proteome is the result of innumerous gene duplication, mutagenesis, drift and selection processes. Whereas random mutagenesis introduces predominantly only gradual changes in protein function, a case can be made that an abrupt switch in function caused by single amino
Subtype selective tetracycline agonists and their application for a two-stage regulatory system.
Christian Berens et al.
Chembiochem : a European journal of chemical biology, 7(9), 1320-1324 (2006-07-28)
Wenjun Zhang et al.
Journal of the American Chemical Society, 130(19), 6068-6069 (2008-04-22)
The cyclohexenone ring A of tetracyclines exhibits unique structural features not observed among other aromatic polyketides. These substitutions include the C2 primary amide, C4 dimethylamine, and the C12a tertiary alcohol. Here we report the identification and reconstitution of the minimum
Marta Gratacós-Cubarsí et al.
Journal of agricultural and food chemistry, 55(11), 4610-4616 (2007-05-10)
Tetracycline (TC) and 4-epitetracycline (4eTC) degradation, as well as anhydrotetracycline (ATC) and 4-epianhydrotetracycline (4eATC) formation, has been evaluated in thermally treated chicken breast, pig loin, and pig loin with added back-fat. Samples containing TC and 4eTC residues were submitted to

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