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Merck
CN

T5783

2,3,4,6-四乙基-O-乙酰基-β-D-吡喃葡萄糖基异硫氰酸酯

derivatization grade (chiral), LiChropur, ≥98.0% (HPLC)

别名:

GITC

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关于此项目

经验公式(希尔记法):
C15H19NO9S
化学文摘社编号:
分子量:
389.38
UNSPSC Code:
41115711
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
56699
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产品名称

2,3,4,6-四乙基-O-乙酰基-β-D-吡喃葡萄糖基异硫氰酸酯, derivatization grade (chiral), LiChropur, ≥98.0% (HPLC)

InChI

1S/C15H19NO9S/c1-7(17)21-5-11-12(22-8(2)18)13(23-9(3)19)14(24-10(4)20)15(25-11)16-6-26/h11-15H,5H2,1-4H3/t11-,12-,13+,14-,15-/m1/s1

SMILES string

CC(=O)OC[C@H]1O[C@@H](N=C=S)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O

InChI key

WOWNQYXIQWQJRJ-UXXRCYHCSA-N

grade

derivatization grade (chiral)

assay

≥98.0% (HPLC)

quality

LiChropur

technique(s)

HPLC: suitable

mp

114-116 °C (lit.)

storage temp.

2-8°C

Quality Level

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Other Notes

探索最适于 HPLCLC-MS 分析的 LiChropur 试剂

Packaging

无底玻璃瓶。内含物装在插入的融合锥内。

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Application

GITC可能已用于非对映异构体的形成以及氨基酸对映体的反相高效液相色谱解析。
用于解析氨基酸衍生物的手性试剂。

General description

2,3,4,6-四-O-乙酰基-β-D-吡喃葡萄糖基异硫氰酸酯是一种手性衍生化试剂,主要与对映体氨基酸发生反应。

pictograms

Health hazardExclamation mark

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Klaas E A Max et al.
Proceedings of the National Academy of Sciences of the United States of America, 115(23), E5334-E5343 (2018-05-20)
Circulating extracellular RNAs (exRNAs) have the potential to serve as biomarkers for a wide range of medical conditions. However, limitations in existing exRNA isolation methods and a lack of knowledge on parameters affecting exRNA variability in human samples may hinder
X Li et al.
Journal of chromatography. B, Biomedical sciences and applications, 742(2), 433-439 (2000-07-20)
A reversed-phase high-performance liquid chromatographic method for the determination of the enantiomers of atenolol in rat hepatic microsome has been developed. Racemic atenolol was extracted from alkalinized rat hepatic microsome by ethyl acetate. The organic layer was dried with anhydrous
Sherry Wang et al.
Journal of pharmaceutical and biomedical analysis, 43(2), 701-707 (2006-09-09)
A stable isotopically labeled (SIL) analogue is believed to be the most appropriate internal standard in a quantitative bioanalytical liquid chromatography/tandem mass spectrometry (LC/MS/MS) assay. It is assumed that a SIL internal standard always compensates for variability in chemical derivatization
J Gal et al.
Journal of pharmacological methods, 16(3), 261-269 (1986-11-01)
Many established and experimental adrenergic agonists are derivatives of 2-aminoethanol with a phenol or catechol moiety in the 1-position. There is considerable interest in the stereochemical aspects of the actions of such chiral drugs. Surprisingly, however, little has been published
Boris Pastorino et al.
Viruses, 12(6) (2020-06-12)
Clinical samples collected in coronavirus disease 19 (COVID-19), patients are commonly manipulated in biosafety level 2 laboratories for molecular diagnostic purposes. Here, we tested French norm NF-EN-14476+A2 derived from European standard EN-14885 to assess the risk of manipulating infectious viruses

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