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Merck
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Key Documents

8.03646

Sigma-Aldrich

Diisopropylamine

for synthesis

동의어(들):

Diisopropylamine, N,N-Diisopropylamine, Bis(1-methylethyl)amine

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About This Item

Linear Formula:
(CH3)2CHNHCH(CH3)2
CAS Number:
Molecular Weight:
101.19
MDL number:
UNSPSC 코드:
12352116
EC 인덱스 번호:
203-558-5
NACRES:
NA.22

vapor pressure

93.33 hPa ( 20 °C)

Quality Level

분석

≥99% (GC)

형태

liquid

autoignition temp.

295 °C

효능

420 mg/kg LD50, oral (Rat)
2900 mg/kg LD50, skin (Rabbit)

expl. lim.

1.1-7.1 % (v/v)

pH

11.8 (20 °C, 6 g/L in H2O)

bp

83-84 °C/1013 hPa

mp

-70 °C

전이 온도

flash point -13.45 °C (DIN 51755 Part 1)

density

0.72 g/cm3 at 20 °C

저장 온도

2-30°C

InChI

1S/C6H15N/c1-5(2)7-6(3)4/h5-7H,1-4H3

InChI key

UAOMVDZJSHZZME-UHFFFAOYSA-N

일반 설명

Diisopropylamine (DIPA) is an aliphatic secondary amine commonly used as an organic base in chemical synthesis.

애플리케이션

Diisopropylamine can be used as:

  • A reagent to synthesize furan, dihydrofuran, or butanolide derivatives by reacting with γ-ketothioesters.
  • A catalyst to prepare aryl disulfides via oxidative coupling of aryl thiols in the presence of air as an oxidant.
  • A base in Pd-catalyzed cross-coupling reactions such as Heck and Sonogashira reaction.

It can also be used as a starting material to prepare lithium diisopropylamide (LDA), a strong non-nucleophilic base widely used in organic synthesis for deprotonation reactions.

픽토그램

FlameSkull and crossbonesCorrosion

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point (°F)

7.8 °F - closed cup

Flash Point (°C)

-13.45 °C - closed cup


시험 성적서(COA)

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Controlled mono and double Heck reactions in water catalyzed by an oxime-derived palladacycle
Botella Luis and Najera C
Tetrahedron Letters, 45(9), 1833-1836 (2004)
Diisopropylamine as a single catalyst in the synthesis of aryl disulfides
Kucinski, K and Hreczycho G
Green Processing and Synthesis, 7(1), 12-15 (2018)
Alexander C Hoepker et al.
Journal of the American Chemical Society, 133(18), 7135-7151 (2011-04-20)
Ortholithiation of 1-chloro-3-(trifluoromethyl)benzene with lithium diisopropylamide (LDA) in tetrahydrofuran at -78 °C displays characteristics of reactions in which aggregation events are rate limiting. Metalation with lithium-chloride-free LDA involves a rate-limiting deaggregation via dimer-based transition structures. The post-rate-limiting proton transfers are

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