3140-73-6 2-Chloro-4,6-dimethoxy-1,3,5-triazine (CDMT) AKSci A719
 
 
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  A719    AKSci Bulk Reagent
2-Chloro-4,6-dimethoxy-1,3,5-triazine (CDMT), 98% (GC)
 



IDENTITY
CAS Number:3140-73-6
MDL Number:MFCD00075607
MF:C5H6ClN3O2
MW:175.57
EINECS:221-541-0
BRN:148988
SPECIFICATIONS & PROPERTIES
Min. Purity Spec:98% (GC)
Physical Form (at 20°C):Solid
Melting Point:71-80°C
Boiling Point:99-100°C(1mmHg)
Long-Term Storage:Store long-term in a cool, dry place
DOT/IATA TRANSPORT INFORMATION
UN #:UN1759
Hazard Class:8; Corrosive
Packing Group:II
A hazmat fee may apply to certain package sizes and shipment methods. Please check pricing table for an indicator of applicable hazmat fees.

REVIEW
 CDMT is a stable, highly reactive peptide coupling agent. It is an useful coupling reagent for the purification of peptides. Catalytic amide-forming reactions of 2-chloro-4,6-dimethoxy-1,3,5-triazine has been reported. Procedure for the preparation of multikilogram quantities of 2-chloro-4,6-dimethoxy-1,3,5-triazine has been reported.

REFERENCES
[1]Tanaka, Tomonari; Organic & Biomolecular Chemistry 2010, V8(22), P5126-5132
[2] Munetaka Kunishima, Takae Ujigawa, Yoshie Nagaoka, Chiho Kawachi, Kazuhito Hioki, Motoo Shiro. Study on 1,3,5-triazine chemistry in dehydrocondensation: gauche effect on the generation of active triazinylammonium species. Chemistry. 2012 Dec 3;18(49):15856-6.
[3] Munetaka Kunishima, Masanori Kitamura, Hiroyuki Tanaka, Ichiro Nakakura, Takahiro Moriya, Kazuhito Hioki. Study of 1,3,5-triazine-based catalytic amide-forming reactions: effect of solvents and basicity of reactants. Chem Pharm Bull (Tokyo). 2013;61(8):882-6.
[4] Jastrzabek K, Bednarek P, Kolesinska B, Kaminski ZJ. Bis(4,6-dimethoxy-1,3,5-triazin-2-yl) ether as coupling reagent for peptide synthesis. Chem Biodivers. 2013 May;10(5):952-61.

GLOBALLY HARMONIZED SYSTEM (GHS)

Pictograms

Signal Word
Danger

Hazard Statements
H314; H317; H318; H401; H411

Precautionary Statements
P260; P264; P272; P273; P280; P301+P330+P331; P303+P361+P353; P304+P340+P310; P305+P351+P338+P310; P333+P313; P363; P391; P405; P501

Current as of July 15, 2025


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CATEGORIES
 Peptide Synthesis >


PubChem