281549
1-Butanol
anhydrous, 99.8%
동의어(들):
n-Butanol, Butyl alcohol
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
CH3(CH2)3OH
CAS 번호:
Molecular Weight:
74.12
UNSPSC Code:
12352001
NACRES:
NA.05
PubChem Substance ID:
EC Number:
200-751-6
Beilstein/REAXYS Number:
969148
MDL number:
Assay:
99.8%
Grade:
anhydrous
Bp:
116-118 °C (lit.)
Vapor pressure:
5 (4 mmHg) at 20 °C hPa
InChI key
LRHPLDYGYMQRHN-UHFFFAOYSA-N
InChI
1S/C4H10O/c1-2-3-4-5/h5H,2-4H2,1H3
SMILES string
CCCCO
grade
anhydrous
vapor density
2.55 (vs air)
vapor pressure
5 (4 mmHg) at 20 °C hPa
assay
99.8%
form
liquid
autoignition temp.
649 °F
expl. lim.
11.2 %
impurities
<0.005% water
evapn. residue
<0.0005%
color
colorless
Quality Level
pH
7 (20 °C, 70 g/L)
bp
116-118 °C (lit.)
mp
−90 °C (lit.)
density
0.81 g/mL at 25 °C (lit.)
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Application
1-Butanol may be used as a solvent for the deoxygenation of O-protected alcohols via Barton-McCombie protocol.
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
flash_point_f
95.0 °F - Pensky-Martens closed cup
flash_point_c
35 °C - Pensky-Martens closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Iwona Żur et al.
Plant reproduction, 26(3), 297-307 (2013-07-05)
Miscanthus × giganteus is a popular energy crop, which due to its hybrid origin is only vegetatively reproduced. Asexual embryogenesis in anther and microspore culture leading to double haploids production could allow to regain the ability for sexual reproduction and to increase
Hong Wang et al.
Advanced materials (Deerfield Beach, Fla.), 28(43), 9545-9549 (2016-09-14)
An organic Schottky barrier diode is created in a single planar PEDOT:Tos film by treating a half of the PEDOT:Tos film with TDAE vapor. Current is rectified in one direction by the Schottky barrier at the junction. The unique planar
Tributylstannane (Bu3SnH)-catalyzed barton-mccombie deoxygenation of alcohols: 3-deoxy-1,2:5,6-bis-O-(1-methylethylidene)-a-D-ribo-hexofuranose
Tormo J and Fu GC
Organic Syntheses, 78, 239-239 (2002)
Shane A Kasten et al.
Chirality, 26(12), 817-824 (2014-10-10)
Chemical warfare nerve agents (CWNAs) are extremely toxic organophosphorus compounds that contain a chiral phosphorus center. Undirected synthesis of G-type CWNAs produces stereoisomers of tabun, sarin, soman, and cyclosarin (GA, GB, GD, and GF, respectively). Analytical-scale methods were developed using
Liquid phase esterification of acrylic acid with 1-butanol catalyzed by solid acid catalysts.
Chen X, et al.
Applied Catalysis A: General, 180(!), 261-269 (1999)
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