4-Dimethylaminopyridine , Promotion Season Now in Store and Free Sample for Testing with Factory Price

  • Chemical Name: 4-Dimethylaminopyridine
  • CAS No.: 1122-58-3
  • Molecular Fomula:C7H10N2
  • Molecular weight:122.17
  • Appearance: White powder
  • Sample: Available


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4-Dimethylaminopyridine CAS# 1122-58-3

Description of 4-Dimethylaminopyridine CAS# 1122-58-3

4-Dimethylaminopyridine (DMAP) is a derivative of pyridine with the chemical formula (CH3)2NC5H4N. This colourless solid is of interest because it is more basic than pyridine, owing to the resonance stabilisation from the NMe2 substituent.
Because of its basicity, DMAP is a useful nucleophilic catalyst for a variety of reactions such as esterifications with anhydrides, the Baylis-Hillman reaction, hydrosilylations, tritylation, the Steglich rearrangement, Staudinger synthesis of β-lactams and many more. Chiral DMAP analogues are used in kinetic resolution experiments of mainly secondary alcohols and Evans auxiliary type amides.

Basic Info of 4-Dimethylaminopyridine CAS# 1122-58-3

Basic Info
Numbering system
Properties
Safety Info
Basic Info

Chemical Name 4-Dimethylaminopyridine
Synonyms 4-Dimethylaminopyrid;AURORA KA-6495;N-(4-Pyridyl)dimethylamine;4-Pyridinamine, N,N-dimethyl-;4-Dimethylaminepyridine;Expand
CAS No. 1122-58-3
Molecular Formula C7H10N2
Molecular Weight 122.16800
PSA 16.13000
LogP 1.14760

Numbering system

EINECS number 214-353-5
MDL number MFCD00006418
BRN number 110354
RTECS number US9230000

Properties

Appearance & Physical State white to yellow crystalline powder
Density 1.012 g/cm3
Boiling Point 162ºC (50 mmHg)
Melting Point 108-113ºC
Flash Point 110ºC
Refractive Index n20/D 1.431
Water Solubility 76 g/L (25 ºC)
Stability Stable. Incompatible with acids, oxidizing agents.
Storage Condition Store in dark
Vapor Pressure 0.431mmHg at 25°C

Safety Info

RTECS US8400000
Hazard Class 8
Safety Statements S26-S28-S36/37/39-S45
HS Code 2933399090
Packing Group II
WGK Germany 3
RIDADR UN 1760/2811
Risk Statements R24/25; R34
Hazard Codes T
Caution Statement P280; P301 + P312 + P330; P302 + P352 + P312; P304 + P340 + P312; P305 + P351 + P338; P337 + P313
Symbol GHS06, GHS08
Hazard Declaration H302; H311; H315; H319; H335; H351
Signal Word Danger

What is 4-Dimethylaminopyridine CAS# 1122-58-3?

With the progress of science and technology and the development of society, chemical products have invariably permeated our daily lives, in medicine, food, cosmetics, electronics, industry, and other areas, becoming an essential part of our lives. One such product is it which has developed particularly rapidly in recent years. Do you know about it?

The official answer:4-Dimethylaminopyridine is a new type of efficient catalyst widely used in chemical synthesis, white crystalline powder with molecular formula C7H10N2.

What’s the application of 4-Dimethylaminopyridine CAS# 1122-58-3?

4-Dimethylaminopyridine is a new type of highly efficient catalyst widely used in chemical synthesis in recent years. 4-Dimethylaminopyridine is a new type of highly efficient catalyst widely used in chemical synthesis in recent years. 4-Dimethylaminopyridine is a new type of highly efficient catalyst widely used in chemical synthesis in recent years. 4-Dimethylaminopyridine is a new type of highly efficient catalyst widely used in chemical synthesis in recent years. 4-Dimethylaminopyridine is a new type of highly efficient catalyst widely used in chemical synthesis in recent years. 4-Dimethylaminopyridine is a new type of highly efficient catalyst widely used in chemical synthesis in recent years. Chemical book acylation (phosphorylation, sulfonylation, carbonylation) of high potential resistance, low reactivity alcohols, and amines, with an activity about 104-6 times that of pyridine. It has a high catalytic capacity for acylation, alkylation, etherification, esterification, and ester exchange in organic synthesis, drug synthesis, pesticides, pharmaceuticals, dyes, fragrances, polymer chemistry, and analytical chemistry, and is extremely effective in improving yields.

Conclusion

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