453021
Allyl alcohol
≥98.5%
Synonym(s):
2-Propen-1-ol
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About This Item
Linear Formula:
CH2=CHCH2OH
CAS Number:
Molecular Weight:
58.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-470-7
Beilstein/REAXYS Number:
605307
MDL number:
Assay:
≥98.5%
vapor density
2 (vs air)
Quality Level
vapor pressure
23.8 mmHg ( 25 °C)
assay
≥98.5%
autoignition temp.
712 °F
expl. lim.
18 %
refractive index
n20/D 1.412 (lit.)
bp
96-98 °C (lit.)
mp
−129 °C (lit.)
density
0.854 g/mL at 25 °C (lit.)
functional group
hydroxyl
SMILES string
OCC=C
InChI
1S/C3H6O/c1-2-3-4/h2,4H,1,3H2
InChI key
XXROGKLTLUQVRX-UHFFFAOYSA-N
Application
Used to induce a mouse model of liver damage that has been used to study the mechanisms of hepatotoxicity and hepatic stem cell-mediated repair.
Packaging
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signalword
Danger
Hazard Classifications
Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 2 - Repr. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
71.6 °F - closed cup
flash_point_c
22 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Muhammad A Khosa et al.
Journal of hazardous materials, 278, 360-371 (2014-07-06)
Chemical modification of chicken feathers (CF) and their subsequent role in arsenic removal from water is presented in this paper. The ground CF were chemically treated with four selective dopants such as poly (ethylene glycol) (PEG) diglycidyl ether, poly (N-isopropylacrylamide)
Hidenori Kinoshita et al.
Organic letters, 6(22), 4085-4088 (2004-10-22)
[reaction: see text] An aqueous biphasic reaction system enables the direct use of allyl alcohol in the Tsuji-Trost reaction without the help of any activating reagents for allyl alcohol. The reaction conditions are neutral to basic, allowing the use of
Madeleine C Warner et al.
Organic letters, 14(19), 5094-5097 (2012-09-26)
A general and efficient route for the synthesis of enantiomerically pure α-substituted ketones and the corresponding lactones has been developed. Ruthenium- and enzyme-catalyzed dynamic kinetic resolution (DKR) with a subsequent Cu-catalyzed α-allylic substitution are the key steps of the route.