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180467

Sigma-Aldrich

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

greener alternative

98%

Sinonimo/i:

1,3-Bis(aminomethyl)cyclohexane

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About This Item

Formula condensata:
C6H10(CH2NH2)2
Numero CAS:
2579-20-6
Peso molecolare:
142.24
Numero CE:
219-941-5
Numero MDL:
MFCD00001522
Codice UNSPSC:
26111700
ID PubChem:
24850870
NACRES:
NA.23

Saggio

98%

Stato

liquid

Caratteristiche più verdi

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

sustainability

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Indice di rifrazione

n20/D 1.493 (lit.)

Densità

0.945 g/mL at 25 °C (lit.)

Categoria alternativa più verde

Enabling,

Stringa SMILE

NCC1CCCC(CN)C1

InChI

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

Descrizione generale

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.

Applicazioni

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.

Pittogrammi

CorrosionExclamation mark
GHS05,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H302 + H312,H314,H412

Classi di pericolo

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

Codice della classe di stoccaggio

8A - Combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

240.8 °F - closed cup

Punto d’infiammabilità (°C)

116 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (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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