52828
1-Hexanol
ReagentPlus®, ≥99.5% (GC)
Sinónimos:
Alcohol hexílico
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Fórmula lineal:
CH3(CH2)5OH
Número CAS:
Peso molecular:
102.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-852-3
Beilstein/REAXYS Number:
969167
MDL number:
Assay:
≥99.5% (GC)
Servicio técnico
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Permítanos ayudarlevapor density
4.5 (vs air)
Quality Level
vapor pressure
1 mmHg ( 25.6 °C)
product line
ReagentPlus®
assay
≥99.5% (GC)
autoignition temp.
559 °F
refractive index
n20/D 1.418
bp
156-157 °C (lit.)
mp
−52 °C (lit.)
density
0.814 g/mL at 25 °C (lit.)
functional group
hydroxyl
SMILES string
CCCCCCO
InChI
1S/C6H14O/c1-2-3-4-5-6-7/h7H,2-6H2,1H3
InChI key
ZSIAUFGUXNUGDI-UHFFFAOYSA-N
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3
Clase de almacenamiento
3 - Flammable liquids
wgk
WGK 1
flash_point_f
140.0 °F - closed cup
flash_point_c
60 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Justin T Mohr et al.
Journal of medicinal chemistry, 48(12), 4172-4176 (2005-06-10)
The polyhydroxyalkanes 1,6,11,16-hexadecanetetraol (1) and 2,7,12,17-octadecanetetraol (2) were synthesized utilizing the thiophene ring as a scaffold to affix the hydroxyalkyl chains by lithiation of the acidic alpha-hydrogens and subsequent desulfurization. Both compounds exhibited significant anesthetic potency, individually and in additivity
Yasumasa Dekishima et al.
Journal of the American Chemical Society, 133(30), 11399-11401 (2011-06-29)
An Escherichia coli strain was engineered to synthesize 1-hexanol from glucose by extending the coenzyme A (CoA)-dependent 1-butanol synthesis reaction sequence catalyzed by exogenous enzymes. The C4-acyl-CoA intermediates were first synthesized via acetyl-CoA acetyltransferase (AtoB), 3-hydroxybutyryl-CoA dehydrogenase (Hbd), crotonase (Crt)
Mir Ali Farajzadeh et al.
Analytica chimica acta, 713, 70-78 (2011-12-28)
In the present work a new, simple, rapid and environmentally friendly dispersive liquid-liquid microextraction (DLLME) method has been developed for extraction/preconcentration of some triazole pesticides in aqueous samples and in grape juice. The extract was analyzed with gas chromatography-flame ionization