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Key Documents

Safety Information

162124

Sigma-Aldrich

N-Butylmethylamine

96%

Synonym(s):

N-Methylbutylamine

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About This Item

Linear Formula:
CH3NH(CH2)3CH3
CAS Number:
Molecular Weight:
87.16
Beilstein:
1209231
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

Assay

96%

refractive index

n20/D 1.3995 (lit.)

bp

90.5-91.5 °C (lit.)

density

0.736 g/mL at 25 °C (lit.)

SMILES string

CCCCNC

InChI

1S/C5H13N/c1-3-4-5-6-2/h6H,3-5H2,1-2H3

InChI key

QCOGKXLOEWLIDC-UHFFFAOYSA-N

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Application

N-Butylmethylamine was used in synthesis of N-n-butyl-N-methyl-N-2-(1-phenyl)propyl-amine and 16α-(bromoalkylamide) derivatives of estradiol.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 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

Regulatory Information

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Certificates of Analysis (COA)

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Ernestine Atangana
Environmental science and pollution research international, 27(9), 9424-9434 (2020-01-10)
The availability of clean water from the already scarce sources is threatened by continuous addition of contaminated industrial and of abattoir waste into watercourses globally. The aim of the current study was to reduce the amount of waste produced, to
A Base-Catalyzed Domino-Isomerization-Hydroamination Reaction-A New Synthetic Route to Amphetamines.
Hartung CG, et al.
Tetrahedron, 56(29), 5157-5162 (2000)
J D Pelletier et al.
Bioorganic & medicinal chemistry, 4(10), 1617-1628 (1996-10-01)
To develop inhibitors of 17 beta-hydroxysteroid dehydrogenase (17 beta-HSD) without residual estrogenic activity, the synthesis of 16 alpha-(bromoalkylamide) derivatives of estradiol was performed starting from a key intermediate aldehyde obtained from commercially available estrone. In addition, series of 16 alpha-(bromoalkyl)

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