308102
N,N-二甲基己胺
98%
别名:
1-（二甲氨基）己烷, N,N-二甲基-1-己胺, N,N-二甲基-N-己胺, N,N-二甲基己胺, 正己基二甲胺
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关于此项目
线性分子式:
CH3(CH2)4CH2N(CH3)2
化学文摘社编号:
分子量:
129.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-491-8
Beilstein/REAXYS Number:
1732757
MDL number:
产品名称
N,N-二甲基己胺, 98%
InChI key
QMHNQZGXPNCMCO-UHFFFAOYSA-N
InChI
1S/C8H19N/c1-4-5-6-7-8-9(2)3/h4-8H2,1-3H3
SMILES string
CCCCCCN(C)C
assay
98%
form
liquid
refractive index
n20/D 1.414 (lit.)
bp
146-150 °C (lit.)
density
0.744 g/mL at 25 °C (lit.)
functional group
amine
Quality Level
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Application
N，N -二甲基己胺作为离子对试剂，用于研究尿苷二磷酸连接中间体在反相介质中保留较差的问题 。还用于测定婴儿食品中的 5 种单磷酸核苷酸（胞苷 5′-一磷酸尿苷 5′-单磷酸腺苷-单磷酸盐，肌苷 5'-一磷酸鸟苷-单磷酸盐）。
General description
游离盐霉素 (Sali) 对肿瘤干细胞 (CSCs) 具有选择性毒性，与添加剂 N,N -二甲基己胺一起被包封到纳米颗粒中 。
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
93.2 °F - closed cup
flash_point_c
34 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Harika Vemula et al.
Analytical biochemistry, 465, 12-19 (2014-08-03)
Bacterial cell wall biosynthesis is the target of several antibiotics and is of interest as a target for new inhibitor development. The cytoplasmic steps of this pathway involve a series of uridine diphosphate (UDP)-linked peptidoglycan intermediates. Quantification of these intermediates
Pilar Viñas et al.
Journal of chromatography. A, 1217(32), 5197-5203 (2010-06-29)
A liquid chromatography with diode array detection coupled to dual electrospray atmospheric pressure chemical ionization time-of-flight mass spectrometry (HPLC/ESI-APCI-TOF-MS) method is described for the rapid determination of five monophosphate nucleotides (cytidine 5'-monophosphate, uridine 5'-monophosphate, adenosine 5'-monophosphate, inosine 5'-monophosphate and guanosine
Peng Zhao et al.
Molecular pharmaceutics, 11(8), 2703-2712 (2014-06-25)
Salinomycin (Sali) has selective toxicity to cancer stem cells (CSCs), a subpopulation of cancer cells that have been recently linked with tumor multidrug resistance (MDR). To utilize its selective toxicity for cancer therapy, we sought to devise a nanoparticle (NP)
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