471291
Isopropylamine
≥99.5%
동의어(들):
2-Aminopropane
로그인조직 및 계약 가격 보기
크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
(CH3)2CHNH2
CAS 번호:
Molecular Weight:
59.11
Beilstein:
605259
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
vapor density
2.04 (vs air)
Quality Level
vapor pressure
9.2 psi ( 20 °C)
분석
≥99.5%
양식
liquid
autoignition temp.
755 °F
expl. lim.
10.4 %
불순물
≤0.1% water
색상
APHA: ≤50
refractive index
n20/D 1.374 (lit.)
bp
33-34 °C (lit.)
density
0.688 g/mL at 20 °C (lit.)
작용기
amine
저장 온도
2-8°C
SMILES string
CC(C)N
InChI
1S/C3H9N/c1-3(2)4/h3H,4H2,1-2H3
InChI key
JJWLVOIRVHMVIS-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
Isopropylamine (i-PrNH2), a primary mine, is a urinary metabolite of propranolol.
애플리케이션
Isopropylamine was used in the following studies:
- Preparation of enantiomerically pure (R and S)- acebutolol.
- As template during the hydrothermal synthesis of SAPO materials.
- Synthesis of bis(salicylaldiminate)nickel(II) complexes.
- Preparation of hydrated, microporous aluminum phosphate AlPO-14.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 1 - Skin Corr. 1A - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point (°F)
<-13.0 °F - closed cup
Flash Point (°C)
<= -25 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles
Isopropylamine, a biologically active deamination product of propranolol in dogs: identification of deuterated and unlabeled isopropylamine by gas chromatography-mass spectrometry.
T Walle et al.
The Journal of pharmacology and experimental therapeutics, 183(3), 508-512 (1972-12-01)
Huaixin Yang et al.
The journal of physical chemistry. B, 109(10), 4464-4469 (2006-07-21)
Differential scanning calorimetry of the hydrated, microporous aluminum phosphate AlPO-14 shows two distinct water losses between room temperature and 120 degrees C, indicating the presence of two types of water in the solid. Multiple-quantum magic angle spinning (MQMAS) (27)Al NMR
Linga Banoth et al.
Chirality, 27(6), 382-391 (2015-05-16)
A new chemoenzymatic route is reported to synthesize acebutolol, a selective β1 adrenergic receptor blocking agent in enantiopure (R and S) forms. The enzymatic kinetic resolution strategy was used to synthesize enantiopure intermediates (R)- and (S)-N-(3-acetyl-4-(3-chloro-2-hydroxypropoxy)phenyl)butyramide from the corresponding racemic
Ethylene oligomerization by novel catalysts based on bis (salicylaldiminate) nickel (II) complexes and organoaluminum co-catalysts.
Carlini C, et al.
Applied Catalysis A: General, 231(1), 307-320 (2002)
On the possibility of incorporating Mn (II) and Cr (III) in SAPO-34 in the presence of isopropylamine as a template.
Rajic N, et al.
Zeolites, 13(4), 384-387 (1993)
자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..
고객지원팀으로 연락바랍니다.