추천 제품
제품 라인
BioReagent
Quality Level
분석
≥99.0% (AT)
형태
crystals
mp
187-193 °C
적합성
suitable for chemiluminescence
SMILES string
Clc1cc(Cl)c(OC(=O)C(=O)Oc2c(Cl)cc(Cl)cc2Cl)c(Cl)c1
InChI
1S/C14H4Cl6O4/c15-5-1-7(17)11(8(18)2-5)23-13(21)14(22)24-12-9(19)3-6(16)4-10(12)20/h1-4H
InChI key
GEVPIWPYWJZSPR-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
분석 메모
Chemiluminescence: Emission: 430 nm (reaction of TCPO with 9,10-Diphenylanthracene and H2O2)
기타 정보
Widely used reagent for the generation of chemiluminescence with H2O2. Used for the determination of fluorescent compounds; Used in the determination of H2O2 with a fluorophore
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Journal of photochemistry and photobiology. B, Biology, 103(2), 87-92 (2011-02-26)
The photodynamic therapy (PDT) is a combination of using a photosensitizer agent, light and oxygen that can cause oxidative cellular damage. This technique is applied in several cases, including for microbial control. The most extensively studied light sources for this
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 59(3), 511-517 (2003-01-14)
The chemiluminescence arising from the reaction of bis(2,4,6-trichlorophenyl)oxalate (TCPO) with hydrogen peroxide in the presence of acriflavine has been studied. The relationship between the chemiluminescence intensity and concentrations of TCPO, H2O2, acriflavine and the base sodium salicylate are reported. The
Evaluation of peroxyoxalate chemiluminescence for determination of enzyme generated peroxide.
Analytical chemistry, 48(7), 1003-1006 (1976-06-01)
Journal of chromatography, 534, 139-149 (1990-12-14)
A sensitive (5 ng/ml) method for the determination of 4-amino-1-hydroxybutane-1,1-bisphosphonic acid in human urine is described. The procedure includes (1) the isolation of the drug from urine by co-precipitation of its calcium salt with endogenous phosphates in the presence of
Analytical Chemistry, 52, 424-424 (1980)
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