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2-Isopropyl-N,2,3-trimethylbutyramide

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2-Isopropyl-N,2,3-trimethylbutyramide Basic information

Product Name:
2-Isopropyl-N,2,3-trimethylbutyramide
Synonyms:
  • FEMA 3804
  • N,2,3-Trimethyl-2-isopropylbutanamide,WS-23
  • 2-ISOPROPYL-N,2,3-TRIMETHYLBUTYRAMIDE
  • N,2,3-TRIMETHYL-2-ISOPROPYLBUTAMIDE
  • N,2,3-TRIMETHYL-2-ISOPROPYLBUTANAMIDE
  • WS-23
  • methyldiisopropylpropionamide
  • 2-Isopropyl-N,2,3-trimethylbutanamide
CAS:
51115-67-4
MF:
C10H21NO
MW:
171.28
EINECS:
256-974-4
Mol File:
51115-67-4.mol
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2-Isopropyl-N,2,3-trimethylbutyramide Chemical Properties

Melting point:
58-61 °C
Boiling point:
bp0.35mm 83-85°
Density 
0.9419 (rough estimate)
vapor pressure 
0.3-0.32Pa at 25℃
refractive index 
1.4621 (estimate)
FEMA 
3804 | 2-ISOPROPYL-N,2,3-TRIMETHYLBUTYRAMIDE
storage temp. 
Sealed in dry,Room Temperature
pka
16.46±0.46(Predicted)
form 
Solid
color 
White to Almost white
Odor
at 25.00 % in dipropylene glycol. mild cooling mentholic minty
Odor Type
minty
JECFA Number
1595
Merck 
14,9716
LogP
2.5 at 25℃ and pH7
CAS DataBase Reference
51115-67-4(CAS DataBase Reference)
EPA Substance Registry System
Butanamide, N,2,3-trimethyl-2-(1-methylethyl)- (51115-67-4)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38-52/53
Safety Statements 
37/39-26
HS Code 
29242990

MSDS

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2-Isopropyl-N,2,3-trimethylbutyramide Usage And Synthesis

Description

2-isopropyl-N,2,3-trimethylbutyramide is one nearly odorless white crystalline powder widely used as a coolant in medicinal preparations, oral care products, foodstuffs, cosmetics, and confection-eye products. It is an artificial synthesis cooling agent and could be synthesized by the Ritter reaction of 2,2-diisopropylpropionitrile (DIPPN) with methanol in the presence of acid. Compared with menthol, WS-23 is characterized by a continuous and long-lasting cooling and refreshing effect with no side effects of burning or stinging sensations. As an important additive in menthol cigarettes, WS-23 can cover up the bitter and astringent taste of cigarettes, make the cigarette feel fresh, improve the coordination and softness of cigarette smoke, and reduce the thorn in the mouth and throat. WS-23 is also compatible with other flavors and cooling agents[1].

Chemical Properties

N,2,3-Trimethyl-2-isopropylbutanamide is a white, crystalline powder,which gives a physiological cooling sensation on skin or mucosa. It is mainly used to create cooling and freshness in oral care preparations.
The material can be prepared by a Ritter reaction using N,2,3-trimethyl-2- isopropylbutyronitrile as the starting material and alkylating agents such as, for example, borates, carbonates, or phosphates.

Chemical Properties

2-Isopropyl-N-2,3-trimethylbutyramide has a cool, mint–menthol-type odor

Uses

2-Isopropyl-N,2,3-trimethylbutanamide is flavored compound and comprising the recount flavored compound for electronic cigarette liquid.

Uses

Physiological coolant in foods, beverages, tobacco products, toiletries, cosmetics and pharmaceuticals.

Definition

ChEBI: N,2,3-Trimethyl-2-(1-methylethyl)butanamide is a fatty amide.

Aroma threshold values

Aroma characteristics at 5.0%: slight cooling impact with little character.

Taste threshold values

Taste characteristics at 20 ppm: high-impacting cooling that lasts on the tongue and palate.

Trade name

Winsense WS-23 (Renessenz).

Synthesis

67029-99-6

51115-67-4

Step 3: 3-isopropyl-4-methyl-2-pentanone (128 g, 0.82 mol) obtained above was dissolved in tetrahydrofuran, followed by the addition of hydroxylamine hydrochloride (1.2 equiv.) and potassium carbonate and the reaction was stirred. The progress of the reaction was monitored by TLC and after confirming that the reaction was complete, water was added to the reaction mixture and extracted with ethyl acetate. The organic phases were combined, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 135 g of crude product. The crude product was dissolved in polyphosphonic acid and heated to 100 °C for 3-8 hours. After the reaction was completed, the reaction solution was neutralized with alkali, extracted again with ethyl acetate, and the organic phase was dried over anhydrous sodium sulfate and then distilled under reduced pressure to remove the solvent. Finally, it was purified by recrystallization to obtain N,2,3-trimethyl-2-isopropylbutyramide 85 g with 99% purity and 49.7% combined yield.

References

[1] Ze-Hong Wu. “Acute and subacute inhalation toxicity assessment of WS-23 in Sprague-Dawley rats.” Journal of Applied Toxicology (2021): 1826–1838.

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