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线性分子式:
C2H5N=C=N(CH2)3N(CH3)3I
化学文摘社编号:
分子量:
297.18
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352116
EC Number:
245-095-1
MDL number:
产品名称
1-(3-二甲基氨丙基)-3-乙基碳二亚胺甲碘盐,
InChI key
AGSKWMRPXWHSPF-UHFFFAOYSA-M
InChI
1S/C9H20N3.HI/c1-5-10-9-11-7-6-8-12(2,3)4;/h5-8H2,1-4H3;1H/q+1;/p-1
SMILES string
[I-].CCN=C=NCCC[N+](C)(C)C
form
powder
reaction suitability
reaction type: Coupling Reactions
mp
97-99 °C (lit.)
application(s)
peptide synthesis
functional group
amine
storage temp.
2-8°C
Quality Level
Application
- 交联剂
反应物用于:
- 酰胺键形成(酰胺化)交联反应
蛋白质的水溶性羧基改性剂。
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Heparin was modified at carboxyl groups by reaction with several pharmacologically important amino-containing compounds in aqueous medium in the presence of 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide. In dependence on the nature of the amine and the ratio of reagents, conjugates containing 36-100% amide and
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