Accéder au contenu
Merck
Toutes les photos(2)

Documents

H13303

Sigma-Aldrich

1-Hexanol

reagent grade, 98%

Synonyme(s) :

Hexyl alcohol

Se connecterpour consulter vos tarifs contractuels et ceux de votre entreprise/organisme
Toutes les photos(2)

About This Item

Formule linéaire :
CH3(CH2)5OH
Numéro CAS:
111-27-3
Poids moléculaire :
102.17
Numéro Beilstein :
969167
Numéro CE :
203-852-3
Numéro MDL:
MFCD00002982
Code UNSPSC :
12352104
ID de substance PubChem :
329815159
Nomenclature NACRES :
NA.21

Qualité

reagent grade

Niveau de qualité

200

Densité de vapeur

4.5 (vs air)

Pression de vapeur

1 mmHg ( 25.6 °C)

Pureté

98%

Forme

liquid

Température d'inflammation spontanée

559 °F

Limite d'explosivité

0.34-6.3 %

Indice de réfraction

n20/D 1.418 (lit.)

Point d'ébullition

156-157 °C (lit.)

Pf

−52 °C (lit.)

Densité

0.814 g/mL at 25 °C (lit.)

Chaîne SMILES 

CCCCCCO

InChI

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

Clé InChI

ZSIAUFGUXNUGDI-UHFFFAOYSA-N

Vous recherchez des produits similaires ? Visite Guide de comparaison des produits

Catégories apparentées

Description générale

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.

Caractéristiques et avantages

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.

Pictogrammes

FlameExclamation mark
GHS02,GHS07

Mention d'avertissement

Warning

Mentions de danger

H226,H302 + H312,H319

Classification des risques

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

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

140.0 °F - closed cup

Point d'éclair (°C)

60 °C - closed cup

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

Déjà en possession de ce produit ?

Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Les clients ont également consulté

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.
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
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
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)
Afficher tous les articles scientifiques apparentés

Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..

Contacter notre Service technique