Přejít k obsahu
Merck
Všechny fotografie(2)

Key Documents

View All Documentation

H13303

Sigma-Aldrich

1-Hexanol

reagent grade, 98%

Synonyma:

Hexyl alcohol

Přihlásitk zobrazení cen stanovených pro organizaci a smluvních cen
Všechny fotografie(2)

About This Item

Lineární vzorec:
CH3(CH2)5OH
Číslo CAS:
111-27-3
Molekulová hmotnost:
102.17
Beilstein/REAXYS Number:
969167
EC Number:
203-852-3
MDL number:
MFCD00002982
UNSPSC Code:
12352104
PubChem Substance ID:
329815159
NACRES:
NA.21

grade

reagent grade

Quality Level

200

vapor density

4.5 (vs air)

vapor pressure

1 mmHg ( 25.6 °C)

assay

98%

form

liquid

autoignition temp.

559 °F

expl. lim.

0.34-6.3 %

refractive index

n20/D 1.418 (lit.)

bp

156-157 °C (lit.)

mp

−52 °C (lit.)

density

0.814 g/mL at 25 °C (lit.)

SMILES string

CCCCCCO

InChI

1S/C6H14O/c1-2-3-4-5-6-7/h7H,2-6H2,1H3

InChI key

ZSIAUFGUXNUGDI-UHFFFAOYSA-N

Hledáte podobné produkty? Navštivte Průvodce porovnáváním produktů

Související kategorie

General description

1-Hexanol is a linear primary alcohol, made up of six carbon atoms and is produced by the oligomerization of ethylene. There is a wide range of uses for 1-hexanol, including plasticizers, antiseptics, fragrances, pharmaceuticals, textiles, and leather finishing agents.

Application

1-Hexanol is used:
  • As an oil phase in the preparation of manganese zinc ferrite nanoparticles by precipitation in reverse microemulsion system.
  • As a solvent in the separation of carboxylic acids and tetrahydrofurfuryl alcohol from water.
  • As a solvent in the synthesis of ZnO (zinc oxide) quantum particles from zinc acetate by precipitation method.

Features and Benefits

1-Hexanol or Hexyl alcohol exhibits high reactivity at a lower temperature due to the alkane-like reaction pathways that begin at a secondary carbon site.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

140.0 °F - closed cup

flash_point_c

60 °C - closed cup

Osvědčení o analýze (COA)

Vyhledejte osvědčení Osvědčení o analýze (COA) zadáním čísla šarže/dávky těchto produktů. Čísla šarže a dávky lze nalézt na štítku produktu za slovy „Lot“ nebo „Batch“.

Již tento produkt vlastníte?

Dokumenty související s produkty, které jste v minulosti zakoupili, byly za účelem usnadnění shromážděny ve vaší Knihovně dokumentů.

Navštívit knihovnu dokumentů

Zákazníci si také prohlíželi

Slide 1 of 5

1 of 5

Heptane ReagentPlus®, 99%

Sigma-Aldrich

H2198

Heptane

1-Pentanol ACS reagent, ≥99%

Sigma-Aldrich

398268

1-Pentanol

1-Octanol anhydrous, ≥99%

Sigma-Aldrich

297887

1-Octanol

N,N′-Dimethylthiourea 99%

Sigma-Aldrich

D188700

N,N′-Dimethylthiourea

1-Nonanol 98%

Sigma-Aldrich

131210

1-Nonanol

Erik Jue et al.
Scientific reports, 10(1), 1940-1940 (2020-02-08)
The success of fundamental and applied nucleic acid (NA) research depends on NA purity, but obtaining pure NAs from raw, unprocessed samples is challenging. Purification using solid-phase NA extractions utilizes sequential additions of lysis and wash buffers followed by elution.
Annie Handler et al.
Cell, 178(1), 60-75 (2019-06-25)
Animals rely on the relative timing of events in their environment to form and update predictive associations, but the molecular and circuit mechanisms for this temporal sensitivity remain incompletely understood. Here, we show that olfactory associations in Drosophila can be
Maria Eugenia Villar et al.
Cell reports, 30(8), 2603-2613 (2020-02-27)
Research on honeybee memory has led to a widely accepted model in which a single pairing of an odor stimulus with sucrose induces memories that are independent of protein synthesis but is unable to form protein-synthesis-dependent long-term memory (LTM). The
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)
Zobrazit všechny související dokumenty

Náš tým vědeckých pracovníků má zkušenosti ve všech oblastech výzkumu, včetně přírodních věd, materiálových věd, chemické syntézy, chromatografie, analytiky a mnoha dalších..

Obraťte se na technický servis.