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Merck

50803

Supelco

Hexylamine

analytical standard

Synonim(y):

1-Aminohexane

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About This Item

Wzór liniowy:
CH3(CH2)5NH2
Numer CAS:
Masa cząsteczkowa:
101.19
Beilstein:
1731298
Numer WE:
Numer MDL:
Kod UNSPSC:
85151701
Identyfikator substancji w PubChem:
NACRES:
NA.24

klasa czystości

analytical standard

Poziom jakości

Próba

≥99.0% (GC)

okres trwałości

limited shelf life, expiry date on the label

granice wybuchowości

2.1-9.3 %

metody

HPLC: suitable
gas chromatography (GC): suitable

zanieczyszczenia

≤0.5% water

współczynnik refrakcji

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

tw

131-132 °C (lit.)

mp

−23 °C (lit.)

gęstość

0.766 g/mL at 25 °C (lit.)

Zastosowanie

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

format

neat

ciąg SMILES

CCCCCCN

InChI

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

Klucz InChI

BMVXCPBXGZKUPN-UHFFFAOYSA-N

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Zastosowanie

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

Danger

Zwroty wskazujące rodzaj zagrożenia

Klasyfikacja zagrożeń

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

Kod klasy składowania

3 - Flammable liquids

Klasa zagrożenia wodnego (WGK)

WGK 1

Temperatura zapłonu (°F)

80.6 °F - closed cup

Temperatura zapłonu (°C)

27 °C - closed cup


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Certyfikaty analizy (CoA)

Lot/Batch Number

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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

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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