์กฐ์ง ๋ฐ ๊ณ์ฝ ๊ฐ๊ฒฉ์ ๋ณด๋ ค๋ฉด ๋ก๊ทธ์ธ๋ฅผ ํด๋ฆญํฉ๋๋ค.
ํฌ๊ธฐ ์ ํ
๋ณด๊ธฐ ๋ณ๊ฒฝ
์ ํ์ ๋ณด (DICE ๋ฐฐ์ก ์ ๋น์ฉ ๋ณ๋)
์คํ์(Hill ํ๊ธฐ๋ฒ):
C32H30N2O3
CAS ๋ฒํธ:
Molecular Weight:
490.59
UNSPSC Code:
12171500
NACRES:
NA.32
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5680006
๊ธฐ์ ์๋น์ค
๋์์ด ํ์ํ์ ๊ฐ์? ์ ํฌ ์๋ จ๋ ๊ณผํ์ ํ์ด ๋์๋๋ฆฌ๊ฒ ์ต๋๋ค.
๋์ ๋ฌธ์form
solid
Quality Level
solubility
methanol: soluble
fluorescence
ฮปex 560 nm; ฮปem 589 nm in methanol
suitability
suitable for fluorescence
SMILES string
[O-]C(=O)c1ccccc1C2=C3C=C4CCC[N+]5=C4C(CCC5)=C3Oc6c7CCCN8CCCc(cc26)c78
InChI
1S/C32H30N2O3/c35-32(36)22-10-2-1-9-21(22)27-25-17-19-7-3-13-33-15-5-11-23(28(19)33)30(25)37-31-24-12-6-16-34-14-4-8-20(29(24)34)18-26(27)31/h1-2,9-10,17-18H,3-8,11-16H2
InChI key
MUSLHCJRTRQOSP-UHFFFAOYSA-N
General description
Rhodamine 101 (Rh101) is a highly stable fluorophore in the rhodamine family.
Application
Rhodamine 101 (Rh101, compoundย 1) has been used:
- as a reference model for analysing extra fluorochromic properties of rhodamine derivatives
- as a reference against thioflavin t (ThT) in the determination of ensemble photophysical properties
- as reference compound for comparing the quantum yields of nanocrystals
Biochem/physiol Actions
Rhodamine 101 (Rh101) is useful as a reference material to measure the fluorescence quantum yield.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
์ ์ฅ ๋ฑ๊ธ
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
๊ฐ์ฅ ์ต์ ๋ฒ์ ์ค ํ๋๋ฅผ ์ ํํ์ธ์:
์ด ์ ํ์ ์ด๋ฏธ ๊ฐ์ง๊ณ ๊ณ์ญ๋๊น?
๋ฌธ์ ๋ผ์ด๋ธ๋ฌ๋ฆฌ์์ ์ต๊ทผ์ ๊ตฌ๋งคํ ์ ํ์ ๋ํ ๋ฌธ์๋ฅผ ์ฐพ์๋ณด์ธ์.
Ryota Iwai et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology (2020-05-21)
Diarylethene derivatives having benzothiophene S,S-dioxide groups undergo turn-on mode fluorescence photoswitching. For the practical application to super-resolution fluorescence microscopy, photoswitchable fluorescent molecules are desired to be resistant against photodegradation. Here we synthesized turn-on mode fluorescent diarylethenes having electron-withdrawing (trifluoromethyl or
Bifunctional fluorescent probes for detection of amyloid aggregates and reactive oxygen species
Needham LM, et al.
Royal Society open science, 5(2), 171399-171399 (2018)
Daniel Aigner et al.
Analytical and bioanalytical chemistry, 400(8), 2475-2485 (2011-01-25)
Asymmetric perylene bisimide (PBI) dyes are prepared and are shown to be suitable for the preparation of fluorescence chemosensors for pH. They carry one amino-functional substituent which introduces pH sensitivity via photoinduced electron transfer (PET) while the other one increases
