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Key Documents

Outros documentos

50803

Supelco

Hexylamine

analytical standard

Sinônimo(s):

1-Aminohexane

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About This Item

Fórmula linear:
CH3(CH2)5NH2
Número CAS:
111-26-2
Peso molecular:
101.19
Beilstein:
1731298
Número CE:
203-851-8
Número MDL:
MFCD00008240
Código UNSPSC:
85151701
ID de substância PubChem:
329757637

grau

analytical standard

Nível de qualidade

100

Ensaio

≥99.0% (GC)

prazo de validade

limited shelf life, expiry date on the label

Lim. expl.

2.1-9.3 %

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

Impurezas

≤0.5% water

índice de refração

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

pb

131-132 °C (lit.)

pf

−23 °C (lit.)

densidade

0.766 g/mL at 25 °C (lit.)

aplicação(ões)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

formato

neat

cadeia de caracteres SMILES

CCCCCCN

InChI

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

chave InChI

BMVXCPBXGZKUPN-UHFFFAOYSA-N

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Categorias relacionadas

Aplicação

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

Palavra indicadora

Danger

Classificações de perigo

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

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

80.6 °F - closed cup

Ponto de fulgor (°C)

27 °C - closed cup

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
BCCD4573
BCBX4173
BCBX0061
BCBV3831
BCBS2818V

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Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

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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
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
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
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
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
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