471526
1-二甲氨基-2-丙醇
≥99%
别名:
N,N-二甲基异丙醇胺
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线性分子式:
CH3CH(OH)CH2N(CH3)2
化学文摘社编号:
分子量:
103.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-556-4
Beilstein/REAXYS Number:
1209244
MDL number:
产品名称
1-二甲氨基-2-丙醇, ≥99%
InChI key
NCXUNZWLEYGQAH-UHFFFAOYSA-N
InChI
1S/C5H13NO/c1-5(7)4-6(2)3/h5,7H,4H2,1-3H3
SMILES string
CC(O)CN(C)C
vapor density
3.6 (vs air)
vapor pressure
8 mmHg ( 20 °C)
assay
≥99%
refractive index
n20/D 1.419 (lit.)
bp
121-127 °C (lit.)
density
0.837 g/mL at 25 °C (lit.)
Quality Level
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Application
1-二甲氨基-2-丙醇溶液可用于合成以下物质：
- 新型不对称2,3,9,10,16,17,23-七（烷氧基）-24-单（二甲氨基烷氧基）酞菁化合物
- 均配的镍（II）氨基醇盐
- 与2,4-戊二酮酸钴（II）的加合物（acac）
General description
1-二甲基氨基-2-丙醇（1DMA2P，DMAPH）是一种叔胺，是一种具有高沸点的二甲基氨基醇。它是可抵抗氮芥细胞毒性的一种有效保护剂以及胆碱摄取的一种抑制剂。已使用停流技术研究了二氧化碳（CO2）与1-二甲基氨基-2-丙醇在水中的均相反应动力学。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
78.8 °F - DIN 51755 Part 1
flash_point_c
26 °C - DIN 51755 Part 1
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Zhaopin Bai et al.
Inorganic chemistry, 49(19), 9005-9011 (2010-09-04)
A new pathway by means of transetherification has been developed to synthesize novel unsymmetrical 2,3,9,10,16,17,23-heptakis(alkoxyl)-24-mono(dimethylaminoalkoxyl)phthalocyanine compounds. Cyclic tetramerization of 4,5-di(alkoxyl)phthalonitrile in refluxing dimethylamino-alcohol with high boiling point such as dimethylaminoethanol (DMAE) and 1-dimethylamino-2-propanol in the presence of lithium and pyrazino[2,3-f][1,10]phenanthroline-2,3-dicarbonitrile
Synthesis and molecular structures of cobalt (II) ?-diketonate complexes as new MOCVD precursors for cobalt oxide films.
Pasko S, et al.
Polyhedron, 23(5), 735-741 (2004)
S A Naujokaitis et al.
Journal of pharmaceutical sciences, 73(1), 34-39 (1984-01-01)
The structure-activity relationships of 2-dimethylaminoethanol and its analogues as protectors against mechlorethamine cytotoxicity and as inhibitors of choline uptake were evaluated. Of a series of inhibitors and protectors, 2-dimethylaminoethanol was the most potent inhibitor of choline uptake and the most
Kinetics of carbon dioxide (CO 2) with ethylenediamine, 3-amino-1-propanol in methanol and ethanol, and with 1-dimethylamino-2-propanol and 3-dimethylamino-1-propanol in water using stopped-flow technique
Kadiwala S, et al.
Chemical Engineering Journal, 179, 262-271 (2012)
Soluble Ni II alkoxides based on dimethylaminoisopropoxide ligands: molecular structure of [Li (Pr i OH) Ni (η 2-OR)2 Cl]2 and of cis-NiCl2 (ROH)2 (R= CHMeCH2NMe2).
Hubert-Pfalzgraf LG, et al.
Polyhedron, 16(24), 4197-4203 (1997)
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