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Key Documents

15090

Sigma-Aldrich

1,4-Bis(2-methylstyryl)benzene

BioReagent, suitable for scintillation, ≥98% (UV)

Sinônimo(s):

Bis-MSB

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About This Item

Fórmula linear:
(CH3C6H4CH=CH)2C6H4
Número CAS:
Peso molecular:
310.43
Beilstein:
2375845
Número CE:
Número MDL:
Código UNSPSC:
12352103
ID de substância PubChem:
NACRES:
NA.32

linha de produto

BioReagent

Ensaio

≥98% (UV)

forma

solid

pf

180-182 °C (lit.)
180-182 °C

fluorescência

λem 416 nm in heptane
λem 419 nm in cyclohexane

adequação

suitable for scintillation

cadeia de caracteres SMILES

Cc1ccccc1\C=C\c2ccc(cc2)\C=C\c3ccccc3C

InChI

1S/C24H22/c1-19-7-3-5-9-23(19)17-15-21-11-13-22(14-12-21)16-18-24-10-6-4-8-20(24)2/h3-18H,1-2H3/b17-15+,18-16+

chave InChI

QKLPIYTUUFFRLV-YTEMWHBBSA-N

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Aplicação

Absolute fluorescence emission in cyclohexane (max): 420nm. Utilized as a scintillator reagent.

produto relacionado

Nº do produto
Descrição
Preços

Pictogramas

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Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

Acute Tox. 4 Oral - Aquatic Chronic 4 - Eye Irrit. 2

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


Certificados de análise (COA)

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Chemphyschem : a European journal of chemical physics and physical chemistry, 9(1), 111-116 (2007-12-12)
The electronic structure and one- and two-photon absorption spectra of four fluorophores, p-bis(o-methoxystyryl)benzene (Bis-MSB), coumarin 307, fluorescein and rhodamine B, commonly used as reference compounds for two-photon absorption spectra, have been theoretically calculated and compared with available experimental data. The
J R Lakowicz et al.
Biophysical chemistry, 47(1), 1-7 (1993-07-01)
We describe the fluorescence spectral properties of p-bis(O-methylstyryl)benzene (bis-MSB) as a standard for time-resolved measurements of two-photon induced fluorescence. Bis-MSB displays the same single exponential intensity decay in several solvents for one- and two-photon excitation. The anisotropy decay displays the
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Schizophyllan, a water-soluble beta-D-glucan elaborated by Schizophyllum commune Fries, was partially depolymerized by ultrasonic irradiation to a low-molecular-weight polysaccharide, designated "sonic-degraded schizophyllan". Both native and degraded polysaccharides exhibited essentially the same antitumor activities against Sarcoma-180 ascites. Both glucans are comprised
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