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Merck
CN

639095

3-(Methylthio)propylamine

97%

Synonym(s):

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

Empirical Formula (Hill Notation):
C4H11NS
CAS Number:
4104-45-4
Molecular Weight:
105.20
NACRES:
NA.22
PubChem Substance ID:
24883004
UNSPSC Code:
12352100
EC Number:
223-875-2
MDL number:
MFCD00041898

Key Documents

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Product Name

3-(Methylthio)propylamine, 97%

InChI key

KKYSBGWCYXYOHA-UHFFFAOYSA-N

InChI

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

SMILES string

CSCCCN

assay

97%

refractive index

n20/D 1.4940 (lit.)

bp

169 °C (lit.)

density

0.938 g/mL at 25 °C (lit.)

functional group

amine
thioether

Quality Level

200

Related Categories

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

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM3670
BCCL6548
BCCH7976
BCCF6568
BCBH8487V

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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
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
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
"The complexation of rhodium (III) with acyclic diaminedithioether (DADTE) ligands"
Akgun Z, et al.
Dalton Transactions, 39(42), 10169-10178 (2010)
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