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639095

Sigma-Aldrich

3-(Methylthio)propylamine

97%

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C4H11NS
Numero CAS:
4104-45-4
Peso molecolare:
105.20
Numero CE:
223-875-2
Numero MDL:
MFCD00041898
Codice UNSPSC:
12352100
ID PubChem:
24883004
NACRES:
NA.22

Livello qualitativo

200

Saggio

97%

Indice di rifrazione

n20/D 1.4940 (lit.)

P. ebollizione

169 °C (lit.)

Densità

0.938 g/mL at 25 °C (lit.)

Gruppo funzionale

amine
thioether

Stringa SMILE

CSCCCN

InChI

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

Categorie correlate

Applicazioni

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

Pittogrammi

CorrosionExclamation mark
GHS05,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H315,H318,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

143.6 °F - closed cup

Punto d’infiammabilità (°C)

62 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificati d'analisi (COA)

Lot/Batch Number
BCCF6568
BCBH8487V
BCBQ7884V
BCBL4389V
BCBC8232V

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USP

1019428

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Isopentylamine 99%

Sigma-Aldrich

126810

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Cysteamine hydrochloride ≥98% (titration)

Sigma-Aldrich

M6500

Cysteamine hydrochloride

3-Methoxypropylamine 99%

Sigma-Aldrich

M25007

3-Methoxypropylamine

Cysteamine ≥98.0% (RT)

Sigma-Aldrich

30070

Cysteamine

2-(Dimethylamino)ethanethiol hydrochloride 95%

Sigma-Aldrich

D141003

2-(Dimethylamino)ethanethiol hydrochloride

Tamás Gáti et al.
Magnetic resonance in chemistry : MRC, 42(7), 600-604 (2004-06-08)
Adducts of four phosphine chalcogenides with the chiral dirhodium complex ([Rh-Rh]) were investigated by variable-temperature 1H and 31P NMR spectroscopy in order to compare their properties as axial ligands. Whereas the selenide (1) and the sulfide (2) are strong ligands
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
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
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
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
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