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제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
CH3(CH2)3OH
CAS 번호:
Molecular Weight:
74.12
UNSPSC Code:
12352001
NACRES:
NA.21
PubChem Substance ID:
EC Number:
200-751-6
Beilstein/REAXYS Number:
969148
MDL number:
Assay:
99.9%
Bp:
116-118 °C (lit.)
Vapor pressure:
5.5 mmHg
vapor density
2.55 (vs air)
Quality Level
vapor pressure
5.5 mmHg
assay
99.9%
autoignition temp.
649 °F
expl. lim.
11.2 %
impurities
≤0.005% Acidity (as Acetic acid), ≤0.020% n-Butyraldehyde, ≤0.05 mg/mL Nonvolatile matter, ≤0.050% Carbonyl (as C=O), ≤0.1% water (Karl Fischer), ≤0.100% Di-n-butyl ether, ≤0.100% Isobutyl alcohol
color
APHA: ≤10
refractive index
n20/D 1.399 (lit.)
pH
7 (20 °C, 70 g/L)
bp
116-118 °C (lit.)
mp
−90 °C (lit.)
solubility
water: soluble
density
0.81 g/mL at 25 °C (lit.)
cation traces
Fe: ≤0.3 ppm
SMILES string
CCCCO
InChI
1S/C4H10O/c1-2-3-4-5/h5H,2-4H2,1H3
InChI key
LRHPLDYGYMQRHN-UHFFFAOYSA-N
General description
1-Butanol is an industrial solvent that can be obtained either from petroleum feedstock or by biomass fermentation. Some of its characteristic properties include high energy content, low vapor pressure and a better capability to combine with gasoline. Synthesis of di-n-butyl ether (DBE) in a fixed-bed flow reactor via dehydration of 1-butanol in the presence of γ-alumina, zeolites, and Amberlyst ion-exchange resins has been investigated. Its thermophysical properties have been calculated. Formation of fatty acid butyl esters (FABE) via transesterification of rapeseed and jatropha oil with 1-butanol in the presence of acid catalyst has been studied under varying conditions.
Application
1-Butanol may be used for the esterification of lactic acid in the presence of lipase from Candida antarctica and hexane solvent.
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signalword
Danger
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Central nervous system, Respiratory system
저장 등급
3 - Flammable liquids
wgk
WGK 1
flash_point_f
95.0 °F - Pensky-Martens closed cup
flash_point_c
35 °C - Pensky-Martens closed cup
Salting-out of acetone, 1-butanol, and ethanol from dilute aqueous solutions.
Xie S, et al.
AIChE Journal, 61(10), 3470-3478 (2015)
Optimization of acid catalyzed transesterification of jatropha and rapeseed oil with 1-butanol.
Bynes AN, et al.
Fuel: The Science and Technology of Fuel and Energy, 137, 94-99 (2014)
Flow reactor synthesis of cetane-enhancing fuel additive from 1-butanol.
Samoilov VO, et al.
Fuel Processing Technology, 140, 312-323 (2015)


