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180467

Sigma-Aldrich

1,3-Cyclohexanebis(methylamine), mixture of isomers

greener alternative

98%

Synonym(s):

1,3-Bis(aminomethyl)cyclohexane

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About This Item

Linear Formula:
C6H10(CH2NH2)2
CAS Number:
2579-20-6
Molecular Weight:
142.24
EC Number:
219-941-5
MDL number:
MFCD00001522
UNSPSC Code:
26111700
PubChem Substance ID:
24850870
NACRES:
NA.23

Assay

98%

form

liquid

greener alternative product characteristics

Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

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refractive index

n20/D 1.493 (lit.)

density

0.945 g/mL at 25 °C (lit.)

greener alternative category

Enabling,

SMILES string

NCC1CCCC(CN)C1

InChI

1S/C8H18N2/c9-5-7-2-1-3-8(4-7)6-10/h7-8H,1-6,9-10H2

InChI key

QLBRROYTTDFLDX-UHFFFAOYSA-N

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency. Find details here.

Application

1,3-Cyclohexanebis(methylamine), mixture of isomers (1,3-BAC), is used as a cross-linking agent that can be used in the formation of fiber-based membranes for the separation of CO2. It can also be used in the synthesis of open-framework bimetallic phosphites for potential usage in molecular sieves and ion exchangers.

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302 + H312,H314,H412

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1A

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 2

Flash Point(F)

240.8 °F - closed cup

Flash Point(C)

116 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCL5634
MKCH5006
MKBP0573V
MKBL5819V
MKBK2438V

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T Hu et al.
Molecular biology of the cell, 10(4), 921-933 (1999-04-10)
We noted previously that certain aminoglycoside antibiotics inhibit the binding of coatomer to Golgi membranes in vitro. The inhibition is mediated in part by two primary amino groups present at the 1 and 3 positions of the 2-deoxystreptamine moiety of
Ishita Neogi et al.
ChemSusChem, 10(19), 3765-3772 (2017-07-29)
A new broadband-emitting 2 D hybrid organic-inorganic perovskite (CyBMA)PbBr
Alice Chen et al.
Biochimica et biophysica acta, 1589(2), 124-139 (2002-05-15)
Retrograde transport dependent on coat protein I (COPI) was impaired using two different approaches and the effects on the retrograde transport of protein toxins were investigated. One approach was to study ldlF cells that express a temperature-sensitive defect in the
Use of aminoglycoside antibiotics and related compounds to study ADP-ribosylation factor (ARF)/coatomer function in Golgi traffic.
R K Draper et al.
Methods in enzymology, 329, 372-379 (2001-02-24)
Kazuki Tainaka et al.
Cell reports, 24(8), 2196-2210 (2018-08-23)
We describe a strategy for developing hydrophilic chemical cocktails for tissue delipidation, decoloring, refractive index (RI) matching, and decalcification, based on comprehensive chemical profiling. More than 1,600 chemicals were screened by a high-throughput evaluation system for each chemical process. The

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