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Merck
CN

284025

二亚乙基三胺五乙酸二酐

98%

别名:

N,N-二[2-(2,6-二氧吗啉代)乙基]氨基乙酸, DTPA 二酐, DTPA 酸酐

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关于此项目

经验公式(希尔记法):
C14H19N3O8
化学文摘社编号:
分子量:
357.32
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1230954
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产品名称

二亚乙基三胺五乙酸二酐, 98%

InChI

1S/C14H19N3O8/c18-10(19)5-15(1-3-16-6-11(20)24-12(21)7-16)2-4-17-8-13(22)25-14(23)9-17/h1-9H2,(H,18,19)

SMILES string

OC(=O)CN(CCN1CC(=O)OC(=O)C1)CCN2CC(=O)OC(=O)C2

InChI key

RAZLJUXJEOEYAM-UHFFFAOYSA-N

assay

98%

form

powder

mp

182-184 °C (lit.)

storage temp.

−20°C

Quality Level

Application

用于合成用作核磁共振成像增强剂的大环配合物和镧系络合物。

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves


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分析证书(COA)

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Yongbo Yang et al.
ACS applied materials & interfaces, 9(28), 23450-23457 (2017-06-29)
A bimodal contrast nanoagent was developed by chelating gadolinium ions to 2-[bis[2-[carboxymethyl-[2-oxo-2-(2-sulfanylethyl-amino)ethyl]amino]ethyl]amino]acetic acid (DTDTPA)-modified CuInS
Farid N Faruqu et al.
Theranostics, 9(6), 1666-1682 (2019-05-01)
Extracellular vesicles, in particular exosomes, have recently gained interest as novel drug delivery vectors due to their biological origin and inherent intercellular biomolecule delivery capability. An in-depth knowledge of their in vivo biodistribution is therefore essential. This work aimed to
Inorganic Chemistry, 33, 5794-5794 (1994)
Yuanyuan Li et al.
Theranostics, 7(19), 4689-4698 (2017-12-01)
Biodegradable polymeric nanomaterials can be directly broken down by intracellular processes, offering a desirable way to solve toxicity issues for cancer diagnosis and treatment. Among them, aliphatic polycarbonates are approved for application in biological fields by the United States Food
Paweł K Halik et al.
Molecules (Basel, Switzerland), 25(16) (2020-08-23)
Aprepitant, a lipophilic and small molecular representative of neurokinin 1 receptor antagonists, is known for its anti-proliferative activity on numerous cancer cell lines that are sensitive to Substance P mitogen action. In the presented research, we developed two novel structural

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