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线性分子式:
(CH3)2CHOH
化学文摘社编号:
分子量:
60.10
UNSPSC Code:
12352001
PubChem Substance ID:
EC Number:
200-661-7
Beilstein/REAXYS Number:
635639
MDL number:
Assay:
≥99.5%
Grade:
ACS reagent
Bp:
82 °C (lit.)
Vapor pressure:
33 mmHg ( 20 °C), 44 mmHg ( 25 °C)
产品名称
2-丙醇, ACS reagent, ≥99.5%
SMILES string
CC(C)O
grade
ACS reagent
vapor density
2.1 (vs air)
vapor pressure
33 mmHg ( 20 °C), 44 mmHg ( 25 °C)
assay
≥99.5%
form
liquid
autoignition temp.
750 °F
expl. lim.
2.0-12.7 %, 93 °C
Quality Level
greener alternative product characteristics
Safer Solvents and Auxiliaries
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
dilution
(for analytical testing)
impurities
≤0.0001 meq/g Titr. acid or base, ≤0.002% carbonyl compounds (propionaldehyde or acetone), ≤0.2% water
evapn. residue
≤0.001%
color
APHA: ≤10
bp
82 °C (lit.)
mp
−89.5 °C (lit.)
solubility
H2O: passes test
density
0.785 g/mL at 25 °C (lit.)
greener alternative category
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General description
Our premium ACS solvents are ideal for routine chemical synthesis, drying, purification, and critical labware cleaning. They meet or exceed the rigorous standards of the American Chemical Society (ACS), ensuring high-quality results for your research needs.
Premium ACS Solvents: Our solvents meet or exceed the stringent standards set by the American Chemical Society, ensuring high quality and reliability for your laboratory applications.
Replicable and Publishable Results: Designed for consistency, our solvents deliver results that can be reliably reproduced, making them ideal for research that requires publication.
Versatile Applications: Suitable for routine chemical synthesis, drying, purification, and critical labware cleaning, our solvents cater to a wide range of research needs in the laboratory.
Premium ACS Solvents: Our solvents meet or exceed the stringent standards set by the American Chemical Society, ensuring high quality and reliability for your laboratory applications.
Replicable and Publishable Results: Designed for consistency, our solvents deliver results that can be reliably reproduced, making them ideal for research that requires publication.
Versatile Applications: Suitable for routine chemical synthesis, drying, purification, and critical labware cleaning, our solvents cater to a wide range of research needs in the laboratory.
Application
2-Propanol may be used in the following processes:
- As a solvent in the synthesis of di- and trisubstituted ortho biaryls by Suzuki-Miyaura cross-coupling reaction.
- As an alternate solvent to benzene in the analysis of total carbonyl compounds in heated and frying oils.
- As a reaction medium in the preparation of cyclic ureas by reacting CO2 with diamines in the presence of pure cerium oxide (CeO2).
Features and Benefits
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This solvent is safe to use and thus aligns with "Safer Solvents and Auxiliaries". Click here for more information.
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
53.6 °F - closed cup
flash_point_c
12.0 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
A modified method for the estimation of total carbonyl compounds in heated and frying oils using 2-propanol as a solvent.
Endo Y, et al.
Journal of the American Oil Chemists' Society, 78(10), 1021-1024 (2001)
A general method for the Suzuki-Miyaura cross-coupling of sterically hindered aryl chlorides: Synthesis of di-and tri-ortho-substituted biaryls in 2-propanol at room temperature.
Navarro O, et al.
Journal of the American Chemical Society, 125(52), 16194-16195 (2003)
Solubility of benzoic acid in acetone, 2-propanol, acetic acid and cyclohexane: Experimental measurement and thermodynamic modeling.
Long B, et al.
Fluid Phase Equilibria, 297(1), 113-120 (2010)
Influence of activated carbon in TiO2 and ZnO mediated photo-assisted degradation of 2-propanol in gas-solid regime.
Matos J, et al.
Applied Catalysis. B, Environmental, 99(1), 170-180 (2010)
Highly efficient synthesis of cyclic ureas from CO2 and diamines by a pure CeO2 catalyst using a 2-propanol solvent.
Tamura M, et al.
Green Chemistry, 15(6), 1567-1577 (2013)
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