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Merck
CN

282804

1,4,8,11-Tetramethyl-1,4,8,11-tetraazacyclotetradecane

98%

Synonym(s):

1,4,8,11-Tetramethylcyclam

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About This Item

Empirical Formula (Hill Notation):
C14H32N4
CAS Number:
Molecular Weight:
256.43
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1210788
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Product Name

1,4,8,11-Tetramethyl-1,4,8,11-tetraazacyclotetradecane, 98%

InChI

1S/C14H32N4/c1-15-7-5-8-17(3)13-14-18(4)10-6-9-16(2)12-11-15/h5-14H2,1-4H3

SMILES string

CN1CCCN(C)CCN(C)CCCN(C)CC1

InChI key

HRFJEOWVAGSJNW-UHFFFAOYSA-N

assay

98%

form

solid

mp

38-42 °C (lit.)

Quality Level

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signalword

Warning

pictograms

Exclamation mark

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

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Ivana Víšová et al.
Macromolecular bioscience, 20(3), e1900351-e1900351 (2020-02-12)
Ultra-low fouling and functionalizable coatings represent emerging surface platforms for various analytical and biomedical applications such as those involving examination of cellular interactions in their native environments. Ultra-low fouling surface platforms as advanced interfaces enabling modulation of behavior of living

Articles

Micro review of reversible addition/fragmentation chain transfer (RAFT) polymerization.

Protocols

We present an article about RAFT, or Reversible Addition/Fragmentation Chain Transfer, which is a form of living radical polymerization.

Polymerization via ATRP procedures demonstrated by Prof. Dave Haddleton's research group at the University of Warwick.

We presents an article featuring procedures that describe polymerization of methyl methacrylate and vinyl acetate homopolymers and a block copolymer as performed by researchers at CSIRO.

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