아크리딘오렌지

아크리딘오렌지
아크리딘오렌지 구조식 이미지
카스 번호:
494-38-2
한글명:
아크리딘오렌지
동의어(한글):
아크리딘오렌지
상품명:
ACRIDINE ORANGE
동의어(영문):
ACRIDINE ORANGE BASE;N3,N3,N6,N6-TetraMethylacridine-3,6-diaMine;SOLVENT ORANGE 15;c.i.46005b;EUCHRYSINE;CI NO 46005;C.I.46005:1;c.i.no.46005:1;waxolineorangea;oranzakridinova
CBNumber:
CB4378880
분자식:
C17H19N3
포뮬러 무게:
265.35
MOL 파일:
494-38-2.mol
MSDS 파일:
SDS

아크리딘오렌지 속성

녹는점
165 °C (dec.)(lit.)
끓는 점
469℃
밀도
1.169
굴절률
1.6080 (estimate)
인화점
237℃
저장 조건
Sealed in dry,Room Temperature
용해도
DMF: 2 mg/ml; DMSO: 20 mg/ml; Ethanol: 0.3 mg/ml; PBS (pH 7.2): 1 mg/ml
물리적 상태
결정성 고체
색상 색인 번호
46005
산도 계수 (pKa)
9.97±0.30(Predicted)
색상
에탄올에서 결정화 된 노란색 바늘 모양의 물질
안정성
감광성
IARC
3 (Vol. 16, Sup 7) 1987

안전

안전지침서 22-24/25
WGK 독일 3
RTECS 번호 AR7600000
독성 mmo-omi 10 mg/L MIBLAO 49,223,80
기존화학 물질 KE-03041

아크리딘오렌지 C화학적 특성, 용도, 생산

물성

분자 내 아크리딘 고리를 가진 염기성 염료를 말한다. 물이나 에탄올에 녹는 분말인데, 이것의 에탄올 용액은 황록색의 형광을 낸다.

용도

주로 가죽 염료로 많이 사용되는데, 후 처리시 제대로 정화되지 않는 폐액 때문에 2차 오염의 피해 가능성이 있다.

개요

Acridine orange is a cell-permeable, nucleic acid-selective fluorescent cationic dye useful for cell cycle determination and detection of cellular autophagy. It exhibits excitation/emission spectra of 502/525, 460/650, and 475/590 nm when bound to dsDNA, bound to ssDNA or RNA, and under acidic conditions, respectively. The ratio of acridine orange emission at 590 to emission at 525 nm can be used to quantify the increase in the number of acidic vesicular organelles observed during cellular autophagy.

정의

ChEBI: A member of the class of aminoacridines that is acridine carrying two dimethylamino substituents at positions 3 and 6. The hydrochloride salt is the fluorescent dye 'acridine orange', used for cell cycle determination.

제조 방법

4,4′-Bis(N,N-dimethyl)aminodiphenylmethane?dinitration, the resultant 4-(4-(Dimethylamino)-3-nitrobenzyl)-N,N-dimethyl-2-nitrobenzenamine?reduction, and acid heating will diamino compound cyclization, then will product oxidation and made free base.

Safety Profile

Poison by subcutaneous route.Questionable carcinogen with experimental tumorigenicand carcinogenic data. Mutation data reported. Whenheated to decomposition it emits toxic fumes of NOx.

Purification Methods

The double salt with ZnCl2 (6g) is dissolved in water (200mL) and stirred with four successive portions (12g each) of Dowex-50 ion-exchange resin (K+ form) to remove the zinc. The solution is then concentrated in vacuum to 20mL, and 100mL of ethanol is added to precipitate KCl which is removed. Ether (160mL) is added to the solution from which, on chilling, the dye crystallises as its chloride. It is separated by centrifugation, washed with chilled ethanol and ether, and dried under vacuum, before being recrystallised from ethanol (100mL) by adding ether (50mL), and chilling. Yield 1g. [Pal & Schubert J Am Chem Soc 84 4384 1962]. It was recrystallised twice as the free base from ethanol or methanol/water by dropwise addition of NaOH (less than 0.1M). The precipitate was washed with water and dried under vacuum. It was dissolved in CHCl3 and chromatographed on alumina: the main sharp band was collected, concentrated and cooled to -20o. The precipitate was filtered off, dried in air, then dried for 2hours under vacuum at 70o. [Stone & Bradley J Am Chem Soc 83 3627 1961, Blauer & Linschitz J Phys Chem 66 453 1962, Albert J Chem Soc 244 1947, Beilstein 22 III/IV 5490, 22/11 V 326.]

아크리딘오렌지 준비 용품 및 원자재

원자재

준비 용품


아크리딘오렌지 공급 업체

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