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50803

Supelco

Hexylamine

analytical standard

Synonyme(s) :

1-Aminohexane

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About This Item

Formule linéaire :
CH3(CH2)5NH2
Numéro CAS:
111-26-2
Poids moléculaire :
101.19
Numéro Beilstein :
1731298
Numéro CE :
203-851-8
Numéro MDL:
MFCD00008240
Code UNSPSC :
85151701
ID de substance PubChem :
329757637
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Pureté

≥99.0% (GC)

Durée de conservation

limited shelf life, expiry date on the label

Limite d'explosivité

2.1-9.3 %

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Impuretés

≤0.5% water

Indice de réfraction

n20/D 1.417-1.419
n20/D 1.418 (lit.)

Point d'ébullition

131-132 °C (lit.)

Pf

−23 °C (lit.)

Densité

0.766 g/mL at 25 °C (lit.)

Application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Format

neat

Chaîne SMILES 

CCCCCCN

InChI

1S/C6H15N/c1-2-3-4-5-6-7/h2-7H2,1H3

Clé InChI

BMVXCPBXGZKUPN-UHFFFAOYSA-N

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Catégories apparentées

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Mention d'avertissement

Danger

Mentions de danger

H226,H301 + H311,H314,H411

Classification des risques

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

80.6 °F - closed cup

Point d'éclair (°C)

27 °C - closed cup

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Certificats d'analyse (COA)

Lot/Batch Number
BCCK7243
BCCH9871
BCCD4573
BCBX4173
BCBX0061

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Consulter la Bibliothèque de documents

J Z Zhou et al.
Oncogene, 34(14), 1831-1842 (2014-05-20)
Extracellular ATP has been shown to either inhibit or promote cancer growth and migration; however, the mechanism underlying this discrepancy remained elusive. Here we demonstrate the divergent roles of ATP and adenosine released by bone osteocytes on breast cancers. We
Maria Notou et al.
Journal of chromatography. A, 1356, 272-276 (2014-07-06)
A novel zone-fluidics/high pressure liquid chromatographic (ZF-HPLC) method is described for the simultaneous determination of six biogenic monoamines, in the presence of hexylamine as internal standard. Automated on-line derivatization of the analytes with naphthalene-2,3-dicarboxaldehyde/cyanide ions was performed using the ZF
Tomáš Taubner et al.
International journal of biological macromolecules, 72, 11-18 (2014-08-12)
Carboxymethylcellulose (CMC) was selected as substrate for amidation based on previous results described for monocarboxy cellulose (MCC) with the aim to prepare highly substituted products. In comparison with MCC containing uronic carboxyl groups at C-6 position, O-carboxymethyl groups in CMC
Ilaria Naldi et al.
PloS one, 9(5), e98101-e98101 (2014-05-24)
Epigenetic events are critical contributors to the pathogenesis of cancer, and targeting epigenetic mechanisms represents a novel strategy in anticancer therapy. Classic demethylating agents, such as 5-Aza-2'-deoxycytidine (Decitabine), hold the potential for reprograming somatic cancer cells demonstrating high therapeutic efficacy
Anton Podjava et al.
European journal of mass spectrometry (Chichester, England), 20(6), 467-475 (2014-01-01)
This paper describes non-covalent complexes between zwitterionic 3-(1-alkyl-3N-imidazolio)- propane-1-sulfonates and different amines. Electrospray ionization (ESI) mass spectrometry and collision- induced dissociation were used to measure the stability of such complexes in solution and in the gas phase. Generally, zwitterionic sulfonates
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