Merck
Todas las fotos(1)

D13208

Sigma-Aldrich

1,4-Diaminobutane

99%

Sinónimos:
1,4-Butanediamine, Putrescine, Tetramethylenediamine
Fórmula lineal:
NH2(CH2)4NH2
Número de CAS:
Peso molecular:
88.15
Beilstein:
605282
Número de EC:
Número MDL:
ID de la sustancia en PubChem:
NACRES:
NA.22

Nivel de calidad

200

ensayo

99%

formulario

solid

lim. expl.

9.08 %

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.)

SMILES string

NCCCCN

InChI

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

InChI key

KIDHWZJUCRJVML-UHFFFAOYSA-N

Gene Information

rat ... Odc1(24609)

¿Está buscando productos similares? Visit Guía de comparación de productos

Categorías relacionadas

Envase

25, 100, 500 g in glass bottle

Aplicación

GABA precursor in many biological systems and synthon for amido-ureas.

pictogramas

CorrosionSkull and crossbones

Palabra de señalización

Danger

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

WGK

WGK 1

Punto de inflamabilidad F

113.0 °F - closed cup

Punto de inflamabilidad C

45 °C - closed cup

Equipo de protección personal

Eyeshields, Faceshields, Gloves, type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges

Certificado de Análisis

Introduzca el número de lote para buscar un certificado de análisis (COA).

Certificado de origen

Introduzca el número de lote para buscar un Certificado de origen (COO).

Journal of the Chemical Society. Perkin Transactions 1, 3179-3179 (1992)
M C de Mello et al.
Neurochemistry international, 22(3), 249-253 (1993-03-01)
Cultured retina cells from chick embryos took up [3H]putrescine and approx 10.8% of the incorporated amine was converted into [3H]GABA. The putrescine-derived GABA accumulated in a pool that was released in the medium at a rate corresponding to 3.66% of
Juhani Jänne et al.
European journal of biochemistry, 271(5), 877-894 (2004-03-11)
The polyamines putrescine, spermidine and spermine are organic cations shown to participate in a bewildering number of cellular reactions, yet their exact functions in intermediary metabolism and specific interactions with cellular components remain largely elusive. Pharmacological interventions have demonstrated convincingly
Chi Yang et al.
PloS one, 7(10), e47314-e47314 (2012-10-17)
The phosphate starvation response in bacteria has been studied extensively for the past few decades and the phosphate-limiting signal is known to be mediated via the PhoBR two-component system. However, the global DNA binding profile of the response regulator PhoB
A Raina et al.
Medical biology, 53(3), 121-147 (1975-06-01)
The biochemistry and biological function of the naturally occurring polyamines, putrescine, spermidine, and spermine, have been reviewed with special reference to animal organisms. These compounds are universally distributed in all living material. Their biosynthesis from ornithine and methionine is accurately

Protocolos

HPLC Analysis of Biogenic Amines on Ascentis® RP-Amide

HPLC Analysis of Biogenic Amines on Ascentis® RP-Amide

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico