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Merck
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Documentos

W424201

Sigma-Aldrich

Amylamine

≥99%, FG

Sinônimo(s):

Pentylamine, 1-Aminopentane, n-Amylamine

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About This Item

Fórmula linear:
CH3(CH2)4NH2
Número CAS:
110-58-7
Peso molecular:
87.16
Número FEMA:
4242
Beilstein:
505953
Número CE:
203-780-2
Número MDL:
MFCD00008236
Código UNSPSC:
12164502
ID de substância PubChem:
24901991
Número de Flavis:
11.021
NACRES:
NA.21

fonte biológica

synthetic

grau

FG

conformidade reg.

EU Regulation 1334/2008 & 872/2012
FDA 21 CFR part 172.515

densidade de vapor

3.01 (vs air)

Ensaio

≥99%

Lim. expl.

22 %

índice de refração

n20/D 1.411 (lit.)

pb

104 °C (lit.)

pf

−50 °C (lit.)

densidade

0.752 g/mL at 25 °C (lit.)

aplicação(ões)

flavors and fragrances

Documentação

see Safety & Documentation for available documents

alérgeno alimentar

no known allergens

Organoléptico

fishy

cadeia de caracteres SMILES

CCCCCN

InChI

1S/C5H13N/c1-2-3-4-5-6/h2-6H2,1H3

chave InChI

DPBLXKKOBLCELK-UHFFFAOYSA-N

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Categorias relacionadas

Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

44.6 °F

Ponto de fulgor (°C)

7 °C

Equipamento de proteção individual

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.

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V V Novokhatny et al.
Thrombosis research, 53(3), 243-252 (1989-02-01)
The interaction of the isolated kringles 4 and 5 from human plasminogen with 6-aminohexanoic acid, pentylamine, pentanoic acid and arginine has been quantitatively characterized by scanning calorimetry and fluorescent spectroscopy. It has been found that the ligands with the positively
C Guffroy et al.
The Journal of pharmacy and pharmacology, 35(7), 416-420 (1983-07-01)
n-Pentylamine is deaminated by homogenates of rat heart. Clorgyline inhibition curves at 10 and 100 microM n-pentylamine indicated that this substrate was deaminated by MAO-A, -B and a clorgyline-resistant amine oxidase sensitive to inhibition by semicarbazide. These results have been
Zan Xie et al.
Journal of chromatography. A, 1104(1-2), 173-178 (2005-12-27)
Volatile organic amine was used as the mobile phase addictive during the separation of four bisphosphonates (alendronate, pamidronate, zoledronic acid and etidronate). An isocratic liquid chromatography method with evaporative light-scattering detection (ELSD) was developed for these bisphosphonates which are not
Y V Matsuka et al.
European journal of biochemistry, 190(1), 93-97 (1990-05-31)
The ligand binding of kringle 1 + 2 + 3 and kringle 1 from human plasminogen has been investigated by fluorescence spectroscopy. Analysis of fluorescence titration of kringle 1 + 2 + 3 with 6-aminohexanoic acid shows that this fragment
J G Liehr et al.
Carcinogenesis, 6(6), 829-836 (1985-06-01)
In a search for the carcinogenic metabolite of diethylstilbestrol, the interactions of 4',4"-diethylstilbestrol quinone with peptides and nucleic acids were investigated. Nonextractable binding of 4',4"-diethylstilbestrol quinone to calf thymus DNA or poly G were observed. However, adduct nucleosides could not
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Protocolos

GC Analysis of Primary Amines on Carbowax® Amine

Separation of Propylamine; Butylamine; Pentylamine; Hexylamine; Heptylamine; Octylamine; Nonylamine; Decylamine

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