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639095

Sigma-Aldrich

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
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.)

functional group

amine
thioether

SMILES string

CSCCCN

InChI

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

InChI key

KKYSBGWCYXYOHA-UHFFFAOYSA-N

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

Signal Word

Danger

Hazard Statements

H315,H318,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

143.6 °F - closed cup

Flash Point(C)

62 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
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
"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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