D144207
1-二甲氨基-2-丙醇
99%
别名:
N,N-二甲基异丙醇胺
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关于此项目
线性分子式:
CH3CH(OH)CH2N(CH3)2
化学文摘社编号:
分子量:
103.16
EC Number:
203-556-4
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1209244
MDL number:
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.)
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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
新产品
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The metabolism and excretion in man of NN-dimethylamino-isopropanol and p-acetamido-benzoic acid after administration of isoprinosine.
P Nielsen et al.
The Journal of pharmacy and pharmacology, 33(8), 549-550 (1981-08-01)
Xiang Zhang et al.
Journal of mass spectrometry : JMS, 42(2), 218-224 (2006-12-19)
The methyl migration between the protonated N,N-dimethylisopropylamine and other neutral aliphatic amines in the gas phase has been investigated by a hybrid external chemical ionization source ion trap mass spectrometer. Similar reactions have been found in the aqueous solution by
Jaimie L Gosselin et al.
The journal of physical chemistry. A, 110(12), 4251-4255 (2006-03-24)
The energy flow and fragmentation dynamics of N,N-dimethylisopropylamine (DMIPA) upon excitation to the 3p Rydberg states has been investigated with use of time-resolved photoelectron and mass spectrometry. The 3p states are short-lived, with a lifetime of 701 +/- 45 fs.
D G Streeter et al.
Drug metabolism and disposition: the biological fate of chemicals, 12(2), 199-203 (1984-03-01)
The principal excretion products derived from radiolabeled N,N-dimethylaminoisopropanol (Dip) and p-acetamidobenzoic acid (PAcBA) components of inosiplex (Isoprinosine) were identified and quantified in urine following single iv and oral administration of the drug in rhesus monkeys. The major metabolite derived from
B Ballantyne et al.
Veterinary and human toxicology, 38(6), 422-426 (1996-12-01)
The acute handling hazards of several alkylalkanolamines were determined by investigating their potential acute toxicity and primary irritancy. Materials studied were N-methylethanolamine (MEA), N, N, -dimethylethanolamine (DMEA), N, N, -dimethylisopropanolamine (DMIPA), N-methyldiethanolamine (MDEA), and tertbutyldiethanolamine (BDEA). All these alkylalkanolamines were
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