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Merck

51799

Supelco

Putrescine

analytical standard

Synonim(y):

1,4-Diaminobutane, 1,4-Butanediamine, Putrescine, Tetramethylenediamine

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About This Item

Wzór liniowy:
NH2(CH2)4NH2
Numer CAS:
Masa cząsteczkowa:
88.15
Beilstein:
605282
Numer WE:
Numer MDL:
Kod UNSPSC:
85151701
Identyfikator substancji w PubChem:
NACRES:
NA.24

klasa czystości

analytical standard

Poziom jakości

Próba

≥98.5% (GC)

okres trwałości

limited shelf life, expiry date on the label

granice wybuchowości

9.08 %

metody

HPLC: suitable
gas chromatography (GC): suitable

współczynnik refrakcji

n20/D 1.457 (lit.)

tw

158-160 °C (lit.)

mp

25-28 °C (lit.)

gęstość

0.877 g/mL at 25 °C (lit.)

Zastosowanie

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

format

neat

temp. przechowywania

2-8°C

ciąg SMILES

NCCCCN

InChI

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

Klucz InChI

KIDHWZJUCRJVML-UHFFFAOYSA-N

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Zastosowanie



  • 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).


Inne uwagi

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

Polecane produkty

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.
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Piktogramy

Skull and crossbonesCorrosion

Hasło ostrzegawcze

Danger

Zwroty wskazujące rodzaj zagrożenia

Klasyfikacja zagrożeń

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

Kod klasy składowania

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

Klasa zagrożenia wodnego (WGK)

WGK 1

Temperatura zapłonu (°F)

113.0 °F - closed cup

Temperatura zapłonu (°C)

45 °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.

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Klienci oglądali również te produkty

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)
The biosynthesis of spermidine and spermine from putrescine and methionine
Tabor H, et al.
The Journal of Biological Chemistry, 233, 907-914 (1958)
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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