82092
1-丙醇
purum, ≥99.0% (GC)
别名:
丙醇
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关于此项目
线性分子式:
CH3CH2CH2OH
化学文摘社编号:
分子量:
60.10
EC Number:
200-746-9
UNSPSC Code:
12352001
PubChem Substance ID:
Beilstein/REAXYS Number:
1098242
MDL number:
Assay:
≥99.0% (GC)
Technique(s):
GC/GC: suitable
Vapor pressure:
10 mmHg ( 147 °C), 14.9 mmHg ( 20 °C)
InChI key
BDERNNFJNOPAEC-UHFFFAOYSA-N
InChI
1S/C3H8O/c1-2-3-4/h4H,2-3H2,1H3
SMILES string
CCCO
Quality Level
vapor pressure
10 mmHg ( 147 °C), 14.9 mmHg ( 20 °C)
grade
purum
assay
≥99.0% (GC)
form
liquid
autoignition temp.
700 °F
expl. lim.
13.7 %
technique(s)
GC/GC: suitable
impurities
≤0.3% water
refractive index
n20/D 1.384 (lit.), n20/D 1.385
pH
8.5 (20 °C, 200 g/L)
mp
−127 °C (lit.)
density
0.804 g/mL at 25 °C (lit.)
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signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 2 - STOT SE 3
target_organs
Central nervous system
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
71.6 °F - closed cup
flash_point_c
22 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
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Eagleson M.
Concise Encyclopedia Chemistry, 896-896 (1994)
Mesoporous alumina (I): comparison of synthesis schemes using anionic, cationic, and non-ionic surfactants.
Ray JC, et al.
Microporous and Mesoporous Materials : The Official Journal of the International Zeolite Association, 100(1), 183-190 (2007)
Dynamics of glass-forming liquids. III. Comparing the dielectric α-and β-relaxation of 1-propanol and o-terphenyl.
Hansen C, et al.
J. Chem. Phys. , 107, 1086-1093 (1997)
Evaluation of Ethanol, 1-Propanol, and 2-Propanol in a Direct Oxidation Polymer-Electrolyte Fuel Cell A Real-Time Mass Spectrometry Study.
Wang J, et al.
Journal of the Electrochemical Society, 142(12), Wang J-Wang J (1995)
Sheba D Bergman et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(33), 10393-10398 (2012-07-13)
A general directed Ru-catalyzed C(sp(3))-H α-alkylation protocol for piperidines (less-reactive substrates than the corresponding five-membered cyclic amines) has been developed. The use of a hindered alcohol (2,4-dimethyl-3-pentanol) as the solvent and catalyst activator, and a catalytic amount of trans-1,2-cyclohexanedicarboxylic acid
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