Basic Fuchsin solution - 0.2% (w/v) pararosaniline hydrochloride solution , CAS No.569-61-9

CAS: 569-61-9 Cat. No.: B108733 Molecular Weight: 323.82 Beilstein Registry Number: 4164603 EC Number: 209-321-2 PubChem CID: 11292
AVAILABLE TO ORDER
GRADE & PURITY 0.2% (w/v) pararosaniline hydrochloride solution
Synonyms
4,4''-Triaminotriphenylmethan-hydrochlorid | C.I. 42500 | C.I. Basic Red 9 (VAN) | C.I. Basic Red 9 monohydrochloride | CI Basic Red 9, monohydrochloride | Fuchsine SPC | Parasaniline | MFCD00001657 | Benzenamine,5-cyclohexadien-1-ylidene)methyl],monohydr
Storage
Argon charged,Desiccated,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
100ml
B108733-100ml
3
$47.90
500ml
B108733-500ml
1

$197.90

$231.90
Save $34.00 (14.66%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

0.2% (w/v) pararosaniline hydrochloride solution for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Argon charged,Desiccated,Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

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

📚

Literature proof

Cited in 15 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
4, 4''-Triaminotriphenylmethan-hydrochlorid | C.I. 42500 | C.I. Basic Red 9 (VAN) | C.I. Basic Red 9 monohydrochloride | CI Basic Red 9, monohydrochloride | Fuchsine SPC | Parasaniline | MFCD00001657 | Benzenamine, 5-cyclohexadien-1-ylidene)methyl], monohydr
Specifications & Purity
0.2% (w/v) pararosaniline hydrochloride solution
Storage
Argon charged, Desiccated, Room temperature
Shipped In
Normal
Names and Identifiers
Canonical SmilesCl.Nc1ccc(cc1)C(\c2ccc(N)cc2)=C3/C=CC(=N)C=C3
IUPAC Name4-[(4-aminophenyl)-(4-iminocyclohexa-2,5-dien-1-ylidene)methyl]aniline;hydrochloride
InChIKeyJUQPZRLQQYSMEQ-UHFFFAOYSA-N
INCHI1S/C19H17N3.ClH/c20-16-7-1-13(2-8-16)19(14-3-9-17(21)10-4-14)15-5-11-18(22)12-6-15;/h1-12,20H,21-22H2;1H
Isomeric SMILES C1=CC(=N)C=CC1=C(C2=CC=C(C=C2)N)C3=CC=C(C=C3)N.Cl
WGK Germany 3
RTECS CX9850100
PubChem CID 11292
Molecular Weight 323.82
Beilstein 4164603
Reaxy-Rn 4164603

Documentation

📋 Safety Data Sheet (SDS)

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

Download SDS →

✅ Certificate of Analysis (COA)

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

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassDiphenylmethanes
Intermediate Tree Nodes Not available
Direct ParentDiphenylmethanes
Alternative Parents Aniline and substituted anilines  Ketimines  Primary amines  Organopnictogen compounds  Hydrochlorides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Diphenylmethane - Aniline or substituted anilines - Ketimine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Primary amine - Organonitrogen compound - Imine - Carbonyl group - Amine - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as diphenylmethanes. These are compounds containing a diphenylmethane moiety, which consists of a methane wherein two hydrogen atoms are replaced by two phenyl groups.
External Descriptors hydrochloride
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TNF Tclin TNF-alpha (1897 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RXRA Tclin Retinoid X receptor alpha (3637 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CXCL8 Tchem Interleukin-8 (642 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GBA1 Tclin Beta-glucocerebrosidase (14647 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALOX15B Tchem Arachidonate 15-lipoxygenase, type II (7244 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NFKB1 Tclin Nuclear factor NF-kappa-B p105 subunit (1459 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A498 (42825 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHN (49357 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CAKI-1 (44928 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CCRF-CEM (65223 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
COLO 205 (50209 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DLD-1 (17511 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DU-145 (51482 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HL-60 (67320 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-29 (80576 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
K562 (73714 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KM12 (47707 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
M14 (47487 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MOLT-4 (49676 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-3 (48710 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-4 (44535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-5 (45555 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-8 (47708 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PC-3 (62116 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RPMI-8226 (44974 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RXF 393 (41971 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SF-295 (48000 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-MEL-2 (46422 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-MEL-28 (48833 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-MEL-5 (47095 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-OV-3 (52876 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SN12C (47755 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SNB-19 (46794 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SNB-78 (14240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TK-10 (45540 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
U-251 (51189 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UACC-257 (46019 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UACC-62 (47335 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UO-31 (46270 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
XF498 (12972 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
786-0 (47912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nr1i2 Nuclear receptor subfamily 1 group I member 2 (14 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
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.

20 results found

Lot NumberCertificate TypeDateItem
B2627375Certificate of AnalysisMar 06, 2026 B108733
B2627376Certificate of AnalysisMar 06, 2026 B108733
E2527455Certificate of AnalysisJun 09, 2025 B108733
E2527456Certificate of AnalysisJun 09, 2025 B108733
I2413379Certificate of AnalysisSep 20, 2024 B108733
I2413378Certificate of AnalysisSep 20, 2024 B108733
F2401131Certificate of AnalysisJun 13, 2024 B108733
F2401074Certificate of AnalysisJun 13, 2024 B108733
G2321915Certificate of AnalysisAug 08, 2023 B108733
G2321906Certificate of AnalysisAug 08, 2023 B108733
D23141100Certificate of AnalysisApr 20, 2023 B108733
D23141170Certificate of AnalysisApr 20, 2023 B108733
B2317181Certificate of AnalysisFeb 21, 2023 B108733
B2317180Certificate of AnalysisFeb 21, 2023 B108733
K2223146Certificate of AnalysisNov 26, 2022 B108733
K2223184Certificate of AnalysisNov 26, 2022 B108733
J2209065Certificate of AnalysisOct 12, 2022 B108733
J2209066Certificate of AnalysisOct 12, 2022 B108733
F2230139Certificate of AnalysisJul 04, 2022 B108733
F2230138Certificate of AnalysisJul 04, 2022 B108733

Show more ⌵

Chemical and Physical Properties
SolubilitySoluble in water (2-3 mg/ml), ethanol (2-25 mg/ml), ether, and diethyl ether.
SensitivityLight sensitive
Melt Point(°C)270℃
Molecular Weight323.800 g/mol
XLogP3
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Exact Mass323.119 Da
Monoisotopic Mass323.119 Da
Topological Polar Surface Area75.900 Ų
Heavy Atom Count23
Formal Charge0
Complexity457.000
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 Count2
Documents & Articles
Citations of This Product
References
1. Xin Yan, Na Zhang, Zhiliang Liu, Chunfang Du.  (2023)  Two-step calcination synthesis of 1T/2H mixed-phase MoS2/g-C3N4 with sulfur defects for efficient removal of Cr(VI) from water.  JOURNAL OF MOLECULAR STRUCTURE,      [PMID:] [10.1016/j.molstruc.2023.137262]
2. Xing Liu, Jianjun Zhou, Shumei Liu, Jianqing Zhao.  (2023)  Synthesis of Phosphorus- and Fluorine-Containing Hyperbranched Imide Oligomers for Flame-Retardant Epoxy Thermosets.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.3c02127]
3. Xie Yifan, Feng Shuo, Deng Linxiao, Cai Aoran, Gan Liyu, Jiang Zifan, Yang Peng, Ye Guilin, Liu Zaiqing, Wen Li, Zhu Qing, Zhang Wanjun, Zhang Zhanpeng, Li Jiahe, Feng Zeyu, Zhang Chutian, Du Wenjie, Xu Lixin, Jiang Jun, Chen Xin, Zou Gang.  (2023)  Inverse design of chiral functional films by a robotic AI-guided system.  Nature Communications,  14  (1): (1-13).  [PMID:37794036] [10.1038/s41467-023-41951-x]
4. Hao Zhang, Pengfei Zhang, Zhiliang Liu, Chunfang Du.  (2023)  Polyoxometalates as highly efficient adsorbents for ciprofloxacin removal: The key role of oxygen vacancies.  JOURNAL OF MOLECULAR STRUCTURE,      [PMID:] [10.1016/j.molstruc.2023.135918]
5. Mao Xu, Qi Tang, Yuchen Liu, Jiaqi Shi, Weiyu Zhang, Chan Guo, Qiuwen Liu, Weiwei Lei, Cheng Chen.  (2023)  Charged Boron Nitride Nanosheet Membranes for Improved Organic Solvent Nanofiltration.  ACS Applied Materials & Interfaces,      [PMID:36820819] [10.1021/acsami.2c20893]
6. Boxuan Yao, Ke Zhang, Xiaoyang Liu, Hua Wei, Zihan Li, Jiarui Zhou, Guangfei Yuan, Xin Wang, Shenghong Yang, Jian Liu.  (2023)  Versatile preparation strategy of negatively charged saccharide-based polymers for selective removal of cationic organic pollutants.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2023.156428]
7. Chaoqiang Ding, Yan Ren, Xinyang Liu, Jingjing Zeng, Xinping Yu, Daxiang Zhou, Yanjie Li.  (2022)  Detection and discrimination of sulfur dioxide using a colorimetric sensor array.  RSC Advances,  12  (40): (25852-25859).  [PMID:36199613] [10.1039/D2RA04251G]
8. Hao Zhang, Min Li, Zhiliang Liu, Xiangchao Zhang, Chunfang Du.  (2022)  Two Keggin-type polyoxometalates used as adsorbents with high efficiency and selectivity toward antibiotics and heavy metals.  JOURNAL OF MOLECULAR STRUCTURE,      [PMID:] [10.1016/j.molstruc.2022.133604]
9. Yaqi Zhang, Haoran Zhang, Shiwei Tian, Longfei Zhang, Wei Li, Wei Wang, Xuhuan Yan, Na Han, Xingxiang Zhang.  (2021)  The Photocatalysis-Enhanced TiO2@HPAN Membrane with High TiO2 Surface Content for Highly Effective Removal of Cationic Dyes.  LANGMUIR,      [PMID:34310152] [10.1021/acs.langmuir.1c01066]
10. Ying Zhang, Jingjing Li, Shengxi Zhang, Weixiang Li, Jin Ouyang, Na Na.  (2021)  Multifunctional Spiky Topological Nanocapsules for the Discrimination and Differential Inhibition of Inflammation and Cancer.  ACS Applied Materials & Interfaces,      [PMID:34048646] [10.1021/acsami.1c04737]
11. Chen Fan, Jiale Yang, You Liang, Hongqiang Dong, Wenbing Zhang, Gang Tang, Yongsong Cao.  (2018)  Effective tuning guanidinium ionic liquid as greener solvent for fast and sensitive determination of auxin herbicides.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2018.08.054]
12. Abdul Ghaffar, Lina Zhang, Xiaoying Zhu, Baoliang Chen.  (2018)  Porous PVdF/GO Nanofibrous Membranes for Selective Separation and Recycling of Charged Organic Dyes from Water.  ENVIRONMENTAL SCIENCE & TECHNOLOGY,      [PMID:29490141] [10.1021/acs.est.7b06081]
13. Haoru Shan, Xueqin Wang, Feihao Shi, Jianhua Yan, Jianyong Yu, Bin Ding.  (2017)  Hierarchical Porous Structured SiO2/SnO2 Nanofibrous Membrane with Superb Flexibility for Molecular Filtration.  ACS Applied Materials & Interfaces,      [PMID:28509531] [10.1021/acsami.7b04518]
14. Shuangshou Wang, Jianing Hui, Yangrui Si, Tianyou Geng, Chunyan Yang, Yanshang Kang, Daojin Li, Mingfu Ye, Tingxuan Yan, Caibo Yue.  (2025)  Deep-eutectic solvent coated paper: A reusable multi-purpose device for rapid visualization, adulteration identification, efficient removal and recycling of dyes in both food and environmental samples.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2024.112625]
15. Chuqiang Que, Hongwei Zhu, Chang Liu, Ziang Qiang, Chen Xu, Minjie Li, Jia Liu, Jing Cao, Pengjian Zuo, Jing Wang, Xin Yang.  (2025)  Nano-size core-shell magnetic SO₃H-functionalized covalent organic frameworks via a functional defect strategy for cationic dye purification: Adsorption behavior and mechanism.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:40816190] [10.1016/j.jhazmat.2025.139516]
Solution Calculators
Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.