256226
N,N-二甲基正辛胺
95%
别名:
1-(二甲氨基)辛烷, N-二甲基正辛胺, Adma 8, DMOA
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关于此项目
线性分子式:
CH3(CH2)7N(CH3)2
化学文摘社编号:
分子量:
157.30
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
230-939-3
Beilstein/REAXYS Number:
1698081
MDL number:
Assay:
95%
Form:
liquid
产品名称
N,N-二甲基正辛胺, 95%
InChI key
UQKAOOAFEFCDGT-UHFFFAOYSA-N
InChI
1S/C10H23N/c1-4-5-6-7-8-9-10-11(2)3/h4-10H2,1-3H3
SMILES string
CCCCCCCCN(C)C
vapor density
5.4 (vs air)
vapor pressure
0.8 mmHg ( 25 °C)
assay
95%
form
liquid
refractive index
n20/D 1.424 (lit.)
bp
195 °C (lit.)
mp
−57 °C (lit.)
density
0.765 g/mL at 25 °C (lit.)
functional group
amine
Quality Level
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Application
N , N -二甲基辛胺已被用于：
- 离子对色谱法测定药物制剂中甲硫酸噻嗪铵的含量
- 反相离子对色谱法分离四环素及其潜在杂质
- 人血浆中 ( R )-和 ( S )-丙吡胺直接分离和定量的流动相
- 毛细管区带电泳中蛋白质络合拆分手性化合物的研究
signalword
Danger
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Repr. 1B - Skin Corr. 1B - Skin Sens. 1
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
156.2 °F - closed cup
flash_point_c
69 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Journal of Chromatography A, 635, 119-119 (1993)
J Hermansson et al.
Journal of chromatography, 336(2), 321-328 (1984-12-12)
The direct resolution and quantitation of (R)- and (S)-disopyramide, isolated from human plasma, was accomplished using a chiral alpha 1-acid glycoprotein column. A LiChrosorb RP-2 column (50 X 3.0 mm I.D.) was used as a precolumn. Phosphate buffer, pH 6.20
E Smet et al.
Journal of pharmaceutical and biomedical analysis, 23(1), 175-183 (2000-07-18)
The phenothiazine derivative thiazinamium methylsulphate is a drug with antihistaminic and anticholinergic properties, often used in some types of obstructive lung diseases. Because there is a lack of chromatographic data available for its determination, the objective of the present investigation
J Hermansson et al.
Journal of pharmaceutical sciences, 71(2), 222-229 (1982-02-01)
Methods are presented for the separation of tetracycline, tetracycline analogs, and their potential impurities by reversed-phase ion-pair chromatography. The mobile phase consisted of a phosphate buffer with tripropylamine or N,N-dimethyloctylamine as counterions and acetonitrile as the organic modifier. The chromatographic
T T Nikiforov et al.
Analytical biochemistry, 227(1), 201-209 (1995-05-01)
A reliable, simple, and cost-effective method for the immobilization of relatively short (12-30 mer) oligonucleotide probes to 96-well polystyrene plates was required in our laboratory for use in DNA hybridization-based assays. We compared three different approaches to achieve this immobilization.
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