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176990

Sigma-Aldrich

tert-Amylamine

98%

Synonym(s):

1,1-Dimethylpropylamine, tert-Pentylamine

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About This Item

Linear Formula:
C2H5C(CH3)2NH2
CAS Number:
594-39-8
Molecular Weight:
87.16
EC Number:
209-839-9
MDL number:
MFCD00008056
UNSPSC Code:
12352100
PubChem Substance ID:
24850613
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.3996 (lit.)

bp

77 °C (lit.)

density

0.746 g/mL at 25 °C (lit.)

SMILES string

CCC(C)(C)N

InChI

1S/C5H13N/c1-4-5(2,3)6/h4,6H2,1-3H3

InChI key

GELMWIVBBPAMIO-UHFFFAOYSA-N

Related Categories

Application

tert-Amylamine was used as a substitute for t-butylamino substituent in cyanobenzylamine derivative.

Signal Word

Danger

Hazard Statements

H225,H301,H314

Hazard Classifications

Acute Tox. 3 Oral - Flam. Liq. 2 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

30.2 °F - closed cup

Flash Point(C)

-1 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Afrooz Shiekhzadeh et al.
Applied biochemistry and biotechnology, 190(2), 506-528 (2019-08-08)
In this paper, a new anticancer Pt (II) complex, cis-[Pt (NH3)2(tertpentylgly)]NO3, was synthesized with glycine-derivative ligand and characterized. Cytotoxicity of this water-soluble Pt complex was studied against human cancer breast cell line of MCF-7. The interaction of human serum albumin
A M Gilbert et al.
Journal of medicinal chemistry, 43(6), 1203-1214 (2000-03-29)
A novel series of benzylamine, potassium channel openers (KCOs) is presented as part of our program toward designing new, bladder-selective compounds for the treatment of urge urinary incontinence (UUI). We have found that the in vitro potency of (R)-4-[3,4-dioxo-2-(1,2, 2-trimethyl-propylamino)-cyclobut-1-enylamino]-3-ethyl-benzo
Mahsa Zahiri et al.
Journal of cellular physiology, 235(2), 1036-1050 (2019-07-06)
In this study, the chemical features of dendritic mesoporous silica nanoparticles (DMSNs) provided the opportunity to design a nanostructure with the capability to intelligently transport the payload to the tumor cells. In this regard, doxorubicin (DOX)-encapsulated DMSNs was electrostatically surface-coated
Radhe Shyam et al.
Biopolymers, 110(6), e23273-e23273 (2019-03-22)
The design of linear peptoid oligomers adopting well-defined secondary structures while mimicking defined peptide primary sequences is a major challenge in the context of drug discovery. To this end, chemists have developed cis-inducing peptoid side chains to build robust polyproline
Jan Leipert et al.
Analytical and bioanalytical chemistry, 410(19), 4737-4748 (2018-02-23)
The identification and quantification of molecules involved in bacterial communication are major prerequisites for the understanding of interspecies interactions at the molecular level. We developed a procedure allowing the determination of 2-heptyl-4(1H)-quinolone (HHQ) and 2-heptyl-3-hydroxy-4(1H)-quinolone (PQS) and the virulence factor

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