Skip to Content
Merck
CN

73753

1,7-Diaza-12-crown-4

≥97.0%

Synonym(s):

1,7-Dioxa-4,10-diazacyclododecane

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Empirical Formula (Hill Notation):
C8H18N2O2
CAS Number:
Molecular Weight:
174.24
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-034-4
Beilstein/REAXYS Number:
606115
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

PWJHXHMUGFXPSN-UHFFFAOYSA-N

InChI

1S/C8H18N2O2/c1-5-11-7-3-10-4-8-12-6-2-9-1/h9-10H,1-8H2

SMILES string

C1COCCNCCOCCN1

assay

≥97.0%

form

crystals

mp

80-84 °C

Application

1,7-Diaza-12-crown-4 can be used to prepare:
  • A ligand named N,N′-bis[(6-carboxy-2-pyridyl)methyl]-1,7-diaza-12-crown-4, which is used to synthesize lanthanide metal complexes applicable as MRI contrast agents.
  • A novel chiral receptor that can be used in the separation of enantiomers using capillary electrophoresis.
  • A fluorescent anthracene based diazacrown ether, which can be used as a photoinduced electron transfer (PET) fluorescent sensor for guest cations.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Lanthanide complexes based on a 1, 7-diaza-12-crown-4 platform containing picolinate pendants: a new structural entry for the design of magnetic resonance imaging contrast agents
Mato-Iglesias M, et al.
Inorganic Chemistry, 47(17), 7840-7851 (2008)
Complexation and fluorescence behavior of diazacrown ether carrying two anthryl pendants
Kubo K, et al.
Talanta, 49(2), 339-344 (1999)
Synthesis of a new chiral receptor containing 1, 7-diaza-12-crown-4 and its application in chiral separation
Wang C, et al.
Synthetic Communications, 33(19), 3381-3386 (2003)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service