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Merck

51799

Supelco

1,4-Diaminobutano

analytical standard

Sinónimos:

1,4-Butanodiamina, Putrescina, Tetrametilenodiamina

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About This Item

Fórmula lineal:
NH2(CH2)4NH2
Número de CAS:
Peso molecular:
88.15
Beilstein:
605282
Número CE:
Número MDL:
Código UNSPSC:
85151701
ID de la sustancia en PubChem:
NACRES:
NA.24

grado

analytical standard

Nivel de calidad

Análisis

≥98.5% (GC)

caducidad

limited shelf life, expiry date on the label

lim. expl.

9.08 %

técnicas

HPLC: suitable
gas chromatography (GC): suitable

índice de refracción

n20/D 1.457 (lit.)

bp

158-160 °C (lit.)

mp

25-28 °C (lit.)

densidad

0.877 g/mL at 25 °C (lit.)

aplicaciones

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

formato

neat

temp. de almacenamiento

2-8°C

cadena SMILES

NCCCCN

InChI

1S/C4H12N2/c5-3-1-2-4-6/h1-6H2

Clave InChI

KIDHWZJUCRJVML-UHFFFAOYSA-N

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Aplicación



  • Putrescine in food analysis: A study demonstrated a novel method for the selective extraction of dietary polyamines, including putrescine, from chicken breast, utilizing lab-on-a-chip electromembrane and dispersive liquid-liquid microextraction techniques for enhanced food analysis (Barzegar et al., 2024).


  • Putrescine in biochemical analysis: The application of Electrostatic Repulsion Hydrophilic Interaction Liquid Chromatography (ERLIC) for the quantitative analysis of polyamines such as putrescine showcases its importance in biochemical assays, providing precise measurement tools for research and development (Dörfel et al., 2024).


Otras notas

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

Productos recomendados

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Pictogramas

Skull and crossbonesCorrosion

Palabra de señalización

Danger

Frases de peligro

Clasificaciones de peligro

Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B

Código de clase de almacenamiento

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

113.0 °F - closed cup

Punto de inflamabilidad (°C)

45 °C - closed cup


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Los clientes también vieron

The biosynthesis of spermidine and spermine from putrescine and methionine
Tabor H, et al.
The Journal of Biological Chemistry, 233, 907-914 (1958)
A comparison of the TLC-densitometry and HPLC method for the determination of biogenic amines in fish and fishery products
Shakila J.R, et al.
Food Chemistry, 75, 255-259 (2001)
Advances and Technical Standards in Neurosurgery, Volume 24 (2012)
Stefan Biastoff et al.
Phytochemistry, 70(15-16), 1708-1718 (2009-08-05)
Putrescine N-methyltransferase (PMT) catalyses S-adenosylmethionine (SAM) dependent methylation of the diamine putrescine. The product N-methylputrescine is the first specific metabolite on the route to nicotine, tropane, and nortropane alkaloids. PMT cDNA sequences were cloned from tobacco species and other Solanaceae
Barry J Shelp et al.
Plant science : an international journal of experimental plant biology, 193-194, 130-135 (2012-07-17)
4-Aminobutyrate (GABA) accumulates in various plant parts, including bulky fruits such as apples, in response to abiotic stress. It is generally believed that the GABA is derived from glutamate, although a contribution from polyamines is possible. Putrescine, but not spermidine

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