Saltar al contenido
Merck
Todas las fotos(1)

Documentos

639095

Sigma-Aldrich

3-(Methylthio)propylamine

97%

Sinónimos:

1-Amino-3-(methylthio)propane, 3-(Methylmercapto)propylamine, 3-(Methylsulfanyl)propylamine, 3-(Methylthio)-1-propanamine, 3-(Methylthio)-1-propylamine, 3-Aminopropyl methyl sulfide, 3-Methylsulfanyl-1-propylamine, 3-Methylsulfanylpropan-1-amine, S-Methylhomocysteamine

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización
Todas las fotos(1)

About This Item

Fórmula empírica (notación de Hill):
C4H11NS
Número de CAS:
4104-45-4
Peso molecular:
105.20
EC Number:
223-875-2
MDL number:
MFCD00041898
UNSPSC Code:
12352100
PubChem Substance ID:
24883004
NACRES:
NA.22

Quality Level

200

assay

97%

refractive index

n20/D 1.4940 (lit.)

bp

169 °C (lit.)

density

0.938 g/mL at 25 °C (lit.)

SMILES string

CSCCCN

InChI

1S/C4H11NS/c1-6-4-2-3-5/h2-5H2,1H3

InChI key

KKYSBGWCYXYOHA-UHFFFAOYSA-N

Categorías relacionadas

Application

3-(Methylthio)propylamine can be used in the synthesis of rhodium(III)complexes involving acyclic diaminedithioether(DADTE)ligands.

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

143.6 °F - closed cup

flash_point_c

62 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

Olga B Morozova et al.
The journal of physical chemistry. A, 109(45), 10459-10466 (2006-07-13)
Using time-resolved chemically induced dynamic nuclear polarization (CIDNP) techniques, we have studied the mechanism of the photoreactions of triplet excited 4-carboxybenzophenone (CBP) with l-methionine (Met) and 3-(methylthio)propylamine (MTPA) in aqueous solution and the details of the formation of CIDNP at
H F Emilie Heng et al.
Journal of food science and technology, 57(3), 1150-1157 (2020-03-04)
The aim of the study was to solve the mystery why sulfur-containing amino acids such as methionine can perform as an antioxidant during frying and hypothesized the antioxidative mechanisms. The results of this study revealed that sulfur-containing amino acids such
Ming-Fu Lin et al.
The Journal of chemical physics, 127(6), 064308-064308 (2007-08-21)
Photodissociation of 3-(methylthio)propylamine and cysteamine, the chromophores of S atom containing amino acid methionine and cysteine, respectively, was studied separately in a molecular beam at 193 nm using multimass ion imaging techniques. Four dissociation channels were observed for 3-(methylthio)propylamine, including
"The complexation of rhodium (III) with acyclic diaminedithioether (DADTE) ligands"
Akgun Z, et al.
Dalton Transactions, 39(42), 10169-10178 (2010)
H Hibasami et al.
Biochemical pharmacology, 38(21), 3673-3676 (1989-11-01)
Methylthiopropylamine (MTPA), an inhibitor of spermidine synthase, markedly induced ornithine decarboxylase (ODC) activity (about 30-fold of the basal level) in human lymphoid leukemia Molt 4B cells. This induction was blocked by the addition of spermidine, spermine or putrescine simultaneously with
Ver todos los artículos relacionados

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