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HCID 61363생성일: 2026년 11월 3일

광택이나는 BLUE G-250

광택이나는BLUEG-250 · BRILLIANT BLUE · BRILLIANT BLUE G · COOMASSIE BRILLIANT BLUE G-250 · G-250 · COOMASSIE BRILLIANT BLUE G · CI 42655 · CBB G-250

https://huagongshe.com/ko/chemical/61363

광택이나는 BLUE G-250 분자 구조식

식별자 및 물리적 특성

CAS No.6104-58-1
분자식C47H48N3NaO7S2
평균 분자량854 g/mol
단동위원소 질량853.28313751 g/mol
SMILESCCOc1ccc(Nc2ccc(C(=C3C=CC(=[N+](CC)Cc4cccc(S(=O)(=O)[O-])c4)C=C3C)c3ccc(N(CC)Cc4cccc(S(=O)(=O)[O-])c4)cc3C)cc2)cc1.[Na+]
InChIKeyRWVGQQGBQSJDQV-UHFFFAOYSA-M
PubChem CID61363
ChEMBLCHEMBL4173394
EC No.228-058-4
현지명광택이나는 BLUE G-250

화학 및 물리적 성질

극성 표면적159
수소 결합 공여자 수1
수소 결합 수용자 수9
회전 가능 결합 수13
무거운 원자 수60
형식 전하0
복잡도1,610
물질 분류Dyes -> Di- and Triaryl Dyes
용해도1mg/mLH2O: 용해성1mg/mL
Human DrugsFDA approved drugs -> Active ingredient
Physical DescriptionBlue crystals[MSDSonline]
녹는점100 °C
밀도1.274[at 20℃]
증기압0.093Pa at 20℃
인화점11 °C
저장 조건2-8°C
물리적 상태고체
색상진한 파란색-보라색-갈색
pH6.4 (20°C, 10g/L in H2O)
용해도물(50mg/ml)과 에탄올(40mg/ml)에 용해됩니다.
BRN5230822
안정성감광성
InChIKeyJFNOCRSXNFZMNT-UHFFFAOYSA-M
SMILES[Na+].[S](=O)(=O)([O-])c1cc(ccc1)CN(CC)c2cc(c(cc2)[C+](c5c(cc(cc5)N(CC)Cc6cc(ccc6)[S](=O)(=O)[O-])C)c3ccc(cc3)Nc4ccc(cc4)OCC)C
LogP(분배 계수)-2.55 at 20℃
EPAC.I. Acid Blue 90 (6104-58-1)

화학적 성질

dark blue-violet-brown crystalline powder

안전 및 규제

GHS 분류This chemical does not meet GHS hazard criteria for 49.3% (101 of 205) of reports.H411 (50.7%): Toxic to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard]P273, P391, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 205 reports by companies from 3 notifications to the ECHA C&L Inventory.
규제 정보Chemical: Benzenemethanaminium, N-[4-[[4-[(4-ethoxyphenyl)amino]phenyl][4-[ethyl[(3-sulfophenyl)methyl]amino]-2-methylphenyl]methylene]-3-methyl-2,5-cyclohexadien-1-ylidene]-N-ethyl-3-sulfo-, hydroxide, inner salt, monosodium saltREACH registered substance: Hydrogen [4-[4-(p-ethoxyanilino)-4'-[ethyl(m-sulphonatobenzyl)amino]-2'-methylbenzhydrylene]-3-methylcyclohexa-2,5-dien-1-ylidene](ethyl)(m-sulphonatobenzyl)ammonium, monosodium salt (EC: 228-058-4)Benzenemethanaminium, N-4-4-(4-ethoxyphenyl)aminophenyl4-ethyl(3-sulfophenyl)methylamino-2-methylphenylmethylene-3-methyl-2,5-cyclohexadien-1-ylidene-N-ethyl-3-sulfo-, inner salt, monosodium salt: Does not have an individual approval but may be used under an appropriate group standard
유해성 요약A skin, eye, and respiratory tract irritant[MSDSonline]
Hazard Classes and CategoriesAquatic Chronic 2 (50.7%)
Drug Induced Liver InjuryDrug Induced Liver Injury Rank (DILIrank 2.0)Brilliant blue gvNo-DILI-concernNo matchDOI:10.1016/j.drudis.2016.02.015
수질 위해 등급(WGK)3
TSCA 등재 상태TSCA listed
관세 코드32041200
기존화학 물질KE-06368
저장 분류11 - Combustible Solids

용도

용도

Brilliant Blue G is used in analytical biochemistry dye and as a P2X7 antagonist. It is also used in protein staining following gel electrophoresis. It is used to prepare the protein reagent for the determination of protein content of the collagenase enzyme isolated from fish waste. It may be employed as stain for the internal limiting membrane (ILM) for the macular hole (MH) and epiretinal membrane (ERM) surgery. It is useful for SDS gels as it readily stains proteins with minimal background color. Protein bands can be visualized during staining. It has been used in the Bradford dye-binding protein assay. A mechanism for dye binding to protein has been proposed, based on measuring Coomassie Brilliant Blue G-250 (CBBG) absorbance spectra during titration of the dye reagent in the absence of protein and its response to different polyamino acids. Brilliant Blue G has been used for determining critical micelle concentration of detergents.

일반 설명

Brilliant Blue G (BBG) is a dye. It has been proposed as a substitute for internal limiting membrane (ILM) peeling.

제조 및 합성 방법

제조 방법

Benzaldehyde (1 Moore) and N-ethyl-N-benzyl-3-methylaniline(2 Moore) condensation, And then sulfonating the product of three acids, and lead oxide, peroxide, and then the reaction with the 4-Ethoxybenzenamine, Benzaldehyde sulfonic acid groups on the phenyl ring is substituted anilino-ethoxy.