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126829

Sigma-Aldrich

3-Methylbenzylamine

98%

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About This Item

Linear Formula:
CH3C6H4CH2NH2
CAS Number:
100-81-2
Molecular Weight:
121.18
EC Number:
202-890-8
MDL number:
MFCD00008118
UNSPSC Code:
12352100
PubChem Substance ID:
24847745
NACRES:
NA.22

Quality Level

100

Assay

98%

form

liquid

refractive index

n20/D 1.536 (lit.)

bp

202-205 °C (lit.)

density

0.966 g/mL at 25 °C (lit.)

SMILES string

Cc1cccc(CN)c1

InChI

1S/C8H11N/c1-7-3-2-4-8(5-7)6-9/h2-5H,6,9H2,1H3

InChI key

RGXUCUWVGKLACF-UHFFFAOYSA-N

Application

3-Methylbenzylamine ({(3-chlorophenyl)methanamine}) has been used as a templating agent in the synthesis of amine-templated materials containing two-dimensional lithium beryllofluoride sheets of the stoichiometry [LiBeF(4)](-). It has also been used to study the chromatographic behavior of a series of substituted aniline and pyridine basic compounds on C18 bonded silica.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

177.8 °F - closed cup

Flash Point(C)

81 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SHBJ7203
SHBF7772V
35696APV
35696AP
35596AP

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Lee A Gerrard et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 9(20), 4936-4942 (2003-10-17)
Four new amine-templated materials, containing two-dimensional lithium beryllofluoride sheets of the stoichiometry [LiBeF(4)](-), have been synthesised under hydrothermal and ambient pressure conditions. [LiBeF(4)][C(6)H(4)(CH(3))CH(2)NH(3)] (1), [LiBeF(4)][C(6)H(4)CH(2)NH(3)Cl] (2), [LiBeF(4)](2)[NH(3)CH(2)CH(2)CH(2)NH(3)] (3), and [LiBeF(4)][C(6)H(5)CH(2)CH(2)CH(2)NH(3)] (4) all contain well-separated anionic sheets containing two different topologies
R LoBrutto et al.
Journal of chromatography. A, 913(1-2), 173-187 (2001-05-18)
The retention of ionogenic bases in liquid chromatography is strongly dependent upon the pH of the mobile phase. Chromatographic behavior of a series of substituted aniline and pyridine basic compounds has been studied on C18 bonded silica using acetonitrile-water (10:90)

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