tert-Amylamine

Name: <I>tert</I>-Amylamine
Brand: ALDRICH
Price: 106 USD
Availability: InStock

98%

Synonym(s):

1,1-Dimethylpropylamine, tert-Pentylamine

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25 G

$106.00

Estimated to ship onNovember 14, 2025fromMILWAUKEE

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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

Key Documents

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Quality Level

100

assay

98%

form

liquid

refractive index

n20/D 1.3996 (lit.)

bp

77 °C (lit.)

density

0.746 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

CCC(C)(C)N

InChI

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

Inchi Key

GELMWIVBBPAMIO-UHFFFAOYSA-N

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This Item	171409	447005	445312
Sigma-Aldrich 176990 tert-Amylamine	Sigma-Aldrich 171409 Amylamine	Sigma-Aldrich 447005 N,N′-Di-tert-butylethylenediamine	Sigma-Aldrich 445312 Hexadecylamine
assay 98%	assay 99%	assay 98%	assay 98%
Quality Level 100	Quality Level 100	Quality Level 100	Quality Level 200
density 0.746 g/mL at 25 °C (lit.)	density 0.752 g/mL at 25 °C (lit.)	density 0.799 g/mL at 25 °C (lit.)	density -
bp 77 °C (lit.)	bp 104 °C (lit.)	bp 196-198 °C (lit.)	bp 330 °C (lit.)
form liquid	form liquid	form liquid	form solid
refractive index n20/D 1.3996 (lit.)	refractive index n20/D 1.411 (lit.)	refractive index n20/D 1.43 (lit.)	refractive index -

Application

tert-Amylamine was used as a substitute for t-butylamino substituent in cyanobenzylamine derivative[1].

Pictograms

GHS02,GHS06,GHS05

signalword

Danger

hcodes

H225,H301,H314

pcodes

P210 - P233 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

30.2 °F - closed cup

flash_point_c

-1 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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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

Design and SAR of novel potassium channel openers targeted for urge urinary incontinence. 2. Selective and potent benzylamino cyclobutenediones.

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

Imaging of the ex vivo transglutaminase activity in liver macrophages of sepsis mice.

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Analytical biochemistry, 597, 113654-113654 (2020-03-07)

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Journal of biomolecular structure & dynamics, 38(8), 2215-2228 (2019-06-18)

Cisplatin, carboplatin and oxaliplatin and their analogs are effective anticancer agents, but their clinical using is limited by some serious side effects. S,S donor ligands such as dithiocarbamates can be used to reduce some side effects. In this study, some

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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

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