Sulforhodamin 101 - ≥98% , CAS No.60311-02-6

CAS: 60311-02-6 Cat. No.: S131262 Summenformel: C31H30N2O7S2 Molekulargewicht: 606.709 Beilstein Registry Number: 3582548 EG-Nummer: 262-159-4 PubChem CID: 122180
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GRADE & PURITY ≥98%
Synonyms
2-(3-oxa-23-aza-9-azoniaheptacyclo[17.7.1.15,9.02,17.04,15.023,27.013,28]octacosa-1(27),2(17),4,9(28),13,15,18-heptaen-16-yl)-5-sulfobenzenesulfonate | SR101
Storage
Vor Licht geschützt, bei -20°C lagern
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Size
Deutschland (EU)
USA*
Price
Qty
25mg
S131262-25mg
4 Auf Lager

37,23€

56,32€
Speichern 19,09 € (33.90%)
100mg
S131262-100mg
2 Auf Lager

117,93€

176,93€
Speichern 59,01 € (33.35%)
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Vor Licht geschützt, bei -20°C lagern Ships Eistruhe + Eispads Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 8 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

Sulforhodamin 101 ist ein rot emittierendes Fluorophor mit einem Extinktionskoeffizienten von 105000. Sulforhodamin 101 wird idealerweise zur Markierung von Astrozyten im Neokortex von Nagetieren verwendet, die mit der Zwei-Photonen-Mikroskopie beobachtet werden können. Darüber hinaus wird Sulforhodamin 101 zur Bestimmung der morphologischen Merkmale von Astrozyten und zur Beobachtung der Assoziation von Astrozyten mit dem kortikalen Mikrogefäßsystem verwendet. Außerdem wird dieses Fluorophor als aktivitätsabhängiger Farbstoff zur Überwachung der regulierten Exozytose verwendet. Andere Studien deuten darauf hin, dass Sulforhodamin 101 die intrinsische neuronale Erregbarkeit und den lang anhaltenden Anstieg der evozierten EPSCs in CA1-Pyramidalneuronen in Hippocampusschnitten erhöhen kann. Sulforhodamin 101 erhöht die evozierten synaptischen N-Methyl-D-Aspartat-Rezeptor-Ströme (NMDAR), die durch den Antagonisten AP-5 blockiert werden können.
Ein rot emittierender Fluorophor, der zur Markierung von Astrozyten verwendet wird.

Specifications

Synonyme
2-(3-oxa-23-aza-9-azoniaheptacyclo[17.7.1.15,9.02,17.04,15.023,27.013,28]octacosa-1(27),2(17),4,9(28),13,15,18-heptaen-16-yl)-5-sulfobenzenesulfonate | SR101
Spezifikationen & Reinheit
≥98%
Biochemische und physiologische Mechanismen
Rotes Standardfluorophor für neurologische Färbungen und Enzymtests. Wird als polarer Tracer für die Untersuchung der Morphologie neuronaler Zellen und der Zell-Zell-Kommunikation verwendet.
Storage
Vor Licht geschützt, bei -20°C lagern
Verschickt in
Eistruhe + Eispads
Hinweis
Weitere Informationen finden Sie im SDB. Benötigen Sie weitere Ratschläge zu Löslichkeit, Verwendung und Handhabung? Besuchen Sie unsere Seite mit den häufig gestellten Fragen (FAQ) für weitere Informationen.
Reinheit
≥98%
Namen und Kennungen
Pubchem Sid488187667
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488187667
Kanonisches LächelnC1CC2=CC3=C(C4=C2N(C1)CCC4)OC5=C6CCC[N+]7=C6C(=CC5=C3C8=C(C=C(C=C8)S(=O)(=O)O)S(=O)(=O)[O-])CCC7
IUPAC Name2-(3-oxa-23-aza-9-azoniaheptacyclo[17.7.1.15,9.02,17.04,15.023,27.013,28]octacosa-1(27),2(17),4,9(28),13,15,18-heptaen-16-yl)-5-sulfobenzenesulfonate
InChIKeyCOIVODZMVVUETJ-UHFFFAOYSA-N
INCHI1S/C31H30N2O7S2/c34-41(35,36)20-9-10-21(26(17-20)42(37,38)39)27-24-15-18-5-1-11-32-13-3-7-22(28(18)32)30(24)40-31-23-8-4-14-33-12-2-6-19(29(23)33)16-25(27)31/h9-10,15-17H,1-8,11-14H2,(H-,34,35,36,37,38,39)
Isomere SMILES C1CC2=CC3=C(C4=C2N(C1)CCC4)OC5=C6CCC[N+]7=C6C(=CC5=C3C8=C(C=C(C=C8)S(=O)(=O)O)S(=O)(=O)[O-])CCC7
PubChem CID 122180
Molekulargewicht 606.709
Beilstein 3582548

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
KlasseBenzopyrans
Subclass1-benzopyrans
Intermediate Tree Nodes Dibenzopyrans
Direct ParentXanthenes
Alternative Parents Benzenesulfonic acids and derivatives  Hydroquinolines  1-sulfo,2-unsubstituted aromatic compounds  Benzenesulfonyl compounds  Dialkylarylamines  Aralkylamines  Heteroaromatic compounds  Sulfonyls  Organosulfonic acids  Oxacyclic compounds  Azacyclic compounds  Organooxygen compounds  Organic zwitterions  Organic oxides  Hydrocarbon derivatives  Organopnictogen compounds  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Xanthene - Tetrahydroquinoline - Benzenesulfonate - Arylsulfonic acid or derivatives - Benzenesulfonyl group - 1-sulfo,2-unsubstituted aromatic compound - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Aralkylamine - Monocyclic benzene moiety - Benzenoid - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Organosulfonic acid - Heteroaromatic compound - Tertiary amine - Oxacycle - Azacycle - Amine - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organic zwitterion - Aromatic heteropolycyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as xanthenes. These are polycyclic aromatic compounds containing a xanthene moiety, which consists of two benzene rings joined to each other by a pyran ring.
External Descriptors organic heteroheptacyclic compound
3D-Struktur
Interaktives chemisches Strukturmodell





Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

13 results found

Lot NumberCertificate TypeDatumArtikel
H2619387Certificate of AnalysisJul 30, 2026 S131262
H2619388Certificate of AnalysisJul 30, 2026 S131262
C2506691Certificate of AnalysisFeb 19, 2025 S131262
C2506714Certificate of AnalysisFeb 19, 2025 S131262
L2510055Certificate of AnalysisFeb 19, 2025 S131262
B2108134Certificate of AnalysisSep 04, 2024 S131262
G2425689Certificate of AnalysisJul 08, 2024 S131262
G2425690Certificate of AnalysisJul 08, 2024 S131262
E2316561Certificate of AnalysisMar 10, 2023 S131262
E2316573Certificate of AnalysisMar 10, 2023 S131262
E2316978Certificate of AnalysisMar 10, 2023 S131262
E2316998Certificate of AnalysisMar 10, 2023 S131262
B2108133Certificate of AnalysisDec 14, 2022 S131262

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Chemische und physikalische Eigenschaften
LöslichkeitSoluble in water (partly), methanol (1 mg/ml), DMSO, and DMF., Soluble in water (partly), methanol (1 mg/ml), DMSO, and DMF.
EmpfindlichkeitMoisture and light sensitive
Molekulargewicht606.700 g/mol
XLogP32.200
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count8
Rotatable Bond Count2
Exact Mass606.149 Da
Monoisotopic Mass606.149 Da
Topological Polar Surface Area144.000 Ų
Heavy Atom Count42
Formal Charge0
Complexity1450.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
FAQs und Artikel
Citations of This Product
Referenzen
1. Feixiang Wang, Shengju Zhou, Youxin Zhang, Yijie Wang, Rui Guo, Haibin Xiao, Xiaofeng Sun.  (2023)  Chiral Phosphorescent Carbonized Polymer Dots Relayed Light-Harvesting System for Color-Tunable Circularly Polarized Room Temperature Phosphorescence.  Small,      [PMID:37994220] [10.1002/smll.202306969]
2. Shiyi Che, Jie Wang, Xiaoyuan Ji, Zhiguo Su, Shaomin Wang, Songping Zhang.  (2020)  Positional assembly of multi-enzyme cascade reaction in polyelectrolyte doped microcapsule through electrospray and layer-by-layer assembly.  Synthetic and Systems Biotechnology,      [PMID:32671236] [10.1016/j.synbio.2020.06.010]
3. Wei Gu, Xueyu Pei, Yuxiao Cheng, Cuiling Zhang, Jidong Zhang, Yinghan Yan, Caiping Ding, Yuezhong Xian.  (2017)  Black Phosphorus Quantum Dots as the Ratiometric Fluorescence Probe for Trace Mercury Ion Detection Based on Inner Filter Effect.  ACS Sensors,      [PMID:28723180] [10.1021/acssensors.7b00102]
4. Zan Long, Bingni Jia, Bingqian Jing, Xiaofeng Liu, Ke Tian, Peng Zhang, Bo Feng, Taiping Qing.  (2025)  Effects of chromophoric dissolved organic matter on the optical properties of different fluorescent probes.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:40107137] [10.1016/j.saa.2025.126064]
5. Mengqi Yang, Yuchen Sun, Xiaonan Wang, Jia Wang, Yongwei Liu, Ailing Zhang, Jinglin Shen, Wei Qi.  (2025)  Fabrication of Light-Harvesting Au Nanoclusters System via Sequential Energy Transfer and the Usage as “On/Off” Switchable Logic Gates.  Advanced Optical Materials,      [PMID:] [10.1002/adom.202403539]
6. Yawen Yu, XinLiu Duan, Xiaorong Wang, Mingyan Yang, Ling Weng, Dalei Li, Teng Liu, Baifang Gong, Zhixia Wang, Huaying Fan.  (2025)  Enhanced therapeutic effects of ginseng-derived exosome-like nanoparticles loaded hyaluronic acid injectable hydrogels for breast tumor treatment.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:40203921] [10.1016/j.ijbiomac.2025.142914]
7. Shan-Ping Wang, Wen-Wen Dong, Pan-Pan Cao, Xue Tian, Dong-Dong Xu, Jun Zhao, Dong-Sheng Li, Qichun Zhang.  (2025)  Reducing Thermal Quenching in Dye@MOF/BN Phosphors for Highly-Efficient White Light Emitting Diodes (WLEDs).  Advanced Optical Materials,      [PMID:] [10.1002/adom.202500439]
8. Lifei Chen, Xuetao Yan, Tianliang Li, Kaixuan Cui, Lixing Lin, Zeyu Li, Yingying Chen, Zhenzhen Li, Lingyan Feng.  (2026)  Interpretable Active Learning for Discovering G-Quadruplex Deep-Eutectic Circularly Polarized Luminescence Materials With High Dissymmetry Factor and Quantum Yield.  Aggregate,  (3): (e70307).  [PMID:] [10.1002/agt2.70307]
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