Erythrosin B - ≥90% , CAS No.15905-32-5

CAS: 15905-32-5 Cat. No.: E359427 Molecular Weight: 835.89 EC Number: 240-046-0
AVAILABLE TO ORDER
GRADE & PURITY ≥90%
Synonyms
C.I. 45430:2 | 3',6'-Dihydroxy-2',4',5',7'-tetraiodospiro(isobenzofuran-1(3H),9'-(9H)xanthene)-3-one | 2, 4,5,7-Tetraiodofluorescein | C20H8I4O5 | J-009558 | SMP2_000049 | E127 | 2',4',5',7'-Tetraiodofluorescein | CI 45430:2 | Erythrosin B | MLS001332406
Storage
Room temperature
Shipped In
Normal
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Size
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Qty
1g
E359427-1g
5
$16.90
5g
E359427-5g
4
$45.90
25g
E359427-25g
1
$140.90
100g
E359427-100g
1
$485.90
500g
E359427-500g
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Why this grade

≥90% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal 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 19 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

It can be used as a dye in fluorescence lifetime imaging. It is also a xanthene dye. It belongs to the family of fluorescein dyes. It plays a major role in inhibiting dopamine uptake and high affinity 3H-ouabain binding and ion transport in synaptosomes from rat caudate nucleus.

Specifications

Synonyms
C.I. 45430:2 | 3', 6'-Dihydroxy-2', 4', 5', 7'-tetraiodospiro(isobenzofuran-1(3H), 9'-(9H)xanthene)-3-one | 2, 4, 5, 7-Tetraiodofluorescein | C20H8I4O5 | J-009558 | SMP2_000049 | E127 | 2', 4', 5', 7'-Tetraiodofluorescein | CI 45430:2 | Erythrosin B | MLS001332406
Specifications & Purity
≥90%
Biochemical and Physiological Mechanisms
Erythrosin B, also called as eosin B, is a xanthene dye. It belongs to the family of fluorescein dyes. It plays a major role in inhibiting dopamine uptake and high affinity 3H-ouabain binding and ion transport in synaptosomes from rat caudate nucleus.
Storage
Room temperature
Shipped In
Normal
Purity
≥90%
Names and Identifiers
Pubchem Sid504750649
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504750649
Canonical SmilesC1=CC=C2C(=C1)C(=O)OC23C4=CC(=C(C(=C4OC5=C(C(=C(C=C35)I)O)I)I)O)I
IUPAC Name3',6'-dihydroxy-2',4',5',7'-tetraiodospiro[2-benzofuran-3,9'-xanthene]-1-one
InChIKeyOALHHIHQOFIMEF-UHFFFAOYSA-N
INCHI1S/C20H8I4O5/c21-11-5-9-17(13(23)15(11)25)28-18-10(6-12(22)16(26)14(18)24)20(9)8-4-2-1-3-7(8)19(27)29-20/h1-6,25-26H
Isomeric SMILES C1=CC=C2C(=C1)C(=O)OC23C4=CC(=C(C(=C4OC5=C(C(=C(C=C35)I)O)I)I)O)I
WGK Germany 2
RTECS LM5940000
Molecular Weight 835.89
Reaxy-Rn 62817
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=62817&ln=

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
ClassBenzopyrans
Subclass1-benzopyrans
Intermediate Tree Nodes Dibenzopyrans
Direct ParentXanthenes
Alternative Parents Diarylethers  Phthalides  Benzofuranones  Isobenzofurans  O-iodophenols  Aryl iodides  Lactones  Carboxylic acid esters  Oxacyclic compounds  Monocarboxylic acids and derivatives  Organoiodides  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Xanthene - Diaryl ether - Isobenzofuranone - Benzofuranone - Phthalide - Isocoumaran - Isobenzofuran - 2-iodophenol - Benzenoid - Aryl halide - Aryl iodide - Carboxylic acid ester - Lactone - Oxacycle - Carboxylic acid derivative - Ether - Monocarboxylic acid or derivatives - Organic oxygen compound - Organohalogen compound - Organoiodide - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Aromatic heteropolycyclic compound
DescriptionThis 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 Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THRB Tclin Thyroid hormone receptor beta-1 (7926 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
DU-145 (51482 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
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
786-0 (47912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI/ADR-RES (33767 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
T47D (39041 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EKVX (44102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H322M (45589 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HCT-116 (91556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HOP-92 (41141 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hs-578T (29457 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H460 (60772 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SF-268 (49410 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
IGROV-1 (47897 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LOX IMVI (44321 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HOP-62 (47048 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-MB-435 (38290 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Malme-3M (44254 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-MB-231 (73002 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SNB-75 (44215 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
ampC Beta-lactamase AmpC (62480 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
West Nile virus (623 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GCN5 Histone acetyltransferase GCN5 (89 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Genome polyprotein (620 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Luciferin 4-monooxygenase (66902 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
pfk 6-phospho-1-fructokinase (7870 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ddn Putative uncharacterized protein (49 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
dengue virus type 2 (2400 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TGR Thioredoxin glutathione reductase (28579 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Large T antigen (1457 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CCT2 T-complex protein 1 subunit beta (5007 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.

8 results found

Lot NumberCertificate TypeDateItem
B2507207Certificate of AnalysisFeb 12, 2025 E359427
G2313176Certificate of AnalysisMay 12, 2023 E359427
H2111253Certificate of AnalysisMay 12, 2023 E359427
H2111254Certificate of AnalysisMay 12, 2023 E359427
H2111255Certificate of AnalysisMay 12, 2023 E359427
H2111256Certificate of AnalysisMay 12, 2023 E359427
H2111262Certificate of AnalysisMay 12, 2023 E359427
L2411107Certificate of AnalysisMay 12, 2023 E359427
Chemical and Physical Properties
SolubilitySoluble in water, spirit, methanol, methyl cellosolve and ethanol.
Melt Point(°C)303°C
Molecular Weight835.900 g/mol
XLogP36.000
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count5
Rotatable Bond Count0
Exact Mass835.655 Da
Monoisotopic Mass835.655 Da
Topological Polar Surface Area76.000 Ų
Heavy Atom Count29
Formal Charge0
Complexity645.000
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
Citations of This Product
References
1. 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]
2. Yuanyuan Li, Haowen Li, Tiancong Wang, Gang Liu, Gang Wang, Miaomiao Liu, Li Pan, Juan He, Kai Li.  (2023)  Surface-molecularly imprinted ratiometric fluorescence sensor for fast, sensitive and selective determination of rhodamine 6G.  DYES AND PIGMENTS,      [PMID:] [10.1016/j.dyepig.2023.111602]
3. Shuangshou Wang, Wenzhi Li, Zhihong Yuan, Qiwen Jin, Zongpeng Ding, Xiaomeng Liu, Mingfu Ye, Jing Gu, Tingxuan Yan, Hongmei Chen, Yang Chen.  (2022)  Semiquantitative naked-eye detection of synthetic food colorants using highly-branched pipette tip as an all-in-one device.  ANALYTICA CHIMICA ACTA,      [PMID:35589223] [10.1016/j.aca.2022.339901]
4. Xuqian Wang, Yuanyuan Peng, Tonghui Xie, Yongkui Zhang, Yabo Wang, Huan Yang.  (2022)  Photocatalytic removal of sulfamethoxazole using yeast biomass-derived NixP/biocarbon composites in the presence of dye sensitizer.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2022.107426]
5. Longming Jin, Lijie Hu, Songmiao Liang, Zhiliang Wang, Guoyang Xu, Xingsheng Yang.  (2022)  A novel organic solvent nanofiltration (OSN) membrane fabricated by Poly(m-phenylene isophthalamide) (PMIA) under large-scale and continuous process.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2022.120259]
6. Muntadher M. Alwan Almijbilee, Yifei Wang, Mao Peng, Aiqun Kong, Jinli Zhang, Wei Li.  (2021)  Ion-binding ameliorates the organic solvents nanofiltration performance of poly (butyl acrylamide-co-divinylbenzene) composites.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2021.119629]
7. Shumin Li, Fan Wu, Rongbin Lin, Jin Wang, Chunxia Li, Zhengquan Li, Jun Jiang, Yujie Xiong.  (2021)  Enabling photocatalytic hydrogen production over Fe-based MOFs by refining band structure with dye sensitization.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2021.132217]
8. Qing Han, Ying Sun, Kangwei Shen, Yan Yan, Xuejun Kang.  (2021)  Rapid determination of seven synthetic dyes in casual snacks based on packed-fibers solid-phase extraction coupled with HPLC-DAD.  FOOD CHEMISTRY,      [PMID:33465694] [10.1016/j.foodchem.2021.129026]
9. Narmadha Manoranjan, Feng Zhang, Zhenyi Wang, Yanping Dong, Wangxi Fang, Yatao Zhang, Yuzhang Zhu, Jian Jin.  (2020)  A Single-Walled Carbon Nanotube/Covalent Organic Framework Nanocomposite Ultrathin Membrane with High Organic Solvent Resistance for Molecule Separation.  ACS Applied Materials & Interfaces,      [PMID:33169985] [10.1021/acsami.0c14825]
10. Yifei Wang, Junjie Gu, Ayang Zhou, Aiqun Kong, Muntadher M. Alwan Almijbilee, Xiaokuo Zheng, Jinli Zhang, Wei Li.  (2020)  Poly[acrylate-co-amide] network composite via photopolymerization for organic solvent nanofiltration separation.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2020.116855]
11. Shiyu Li, Zhongying Zhang, Jingdong Peng, Xiang Wang, Dengying Long, Hong Xian, Ranxi Ni, Huanjun Peng, Jun Chen.  (2019)  High-performance liquid chromatography associated with resonance Rayleigh scattering spectral study of the interactions of palladium(II)–antimigraine chelates with Erythrosin B and their analytical applications.  NEW JOURNAL OF CHEMISTRY,  44  (7): (3078-3086).  [PMID:] [10.1039/C9NJ02390A]
12. Xiaokuo Zheng, Ayang Zhou, Yifei Wang, Xiao He, Shuchun Zhao, Jinli Zhang, Wei Li.  (2019)  Modulating hydrophobicity of composite polyamide membranes to enhance the organic solvent nanofiltration.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2019.04.078]
13. Zhen Cheng, Lingling Du, Panpan Zhu, Qian Chen, Kejun Tan.  (2018)  An erythrosin B-based “turn on” fluorescent sensor for detecting perfluorooctane sulfonate and perfluorooctanoic acid in environmental water samples.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:29758514] [10.1016/j.saa.2018.05.013]
14. Piyong Zhang, Ting Song, Tingting Wang, Heping Zeng.  (2017)  Enhancement of hydrogen production of a Cu–TiO2 nanocomposite photocatalyst combined with broad spectrum absorption sensitizer Erythrosin B.  RSC Advances,  (29): (17873-17881).  [PMID:] [10.1039/C6RA27686E]
15. Dan Liu, Jingdong Peng, Shaopu Liu, Mingqiong Zhou, Jing Zhang, Aiping Li.  (2016)  Resonance Rayleigh scattering technique as a detection method for the RP-HPLC determination of local anaesthetics in human urine.  LUMINESCENCE,  32  (1): (4-10).  [PMID:27145989] [10.1002/bio.3140]
16. Qing Han, Xi Wang, Zaiyue Yang, Wanying Zhu, Xuemin Zhou, Huijun Jiang.  (2014)  Fe3O4@rGO doped molecularly imprinted polymer membrane based on magnetic field directed self-assembly for the determination of amaranth.  TALANTA,      [PMID:24725870] [10.1016/j.talanta.2014.01.060]
17. Tingwei Cai, Hanchang Hu, Qiangqiang Zhao, Zhong Zhang, Jinxin He.  (2024)  Investigation of heavy atom effects and pH sensitivity on the photocatalytic cross-dehydrogenative coupling reaction of halogenated fluorescein dyes.  DYES AND PIGMENTS,      [PMID:] [10.1016/j.dyepig.2024.112437]
18. Bingzhi Li, Yiqi Wang, Linpin Luo, Liang Zhang, Yiya Ping, Bangfeng Fu, Wetao Zhang, Lei Liu, Jianlong Wang.  (2025)  Polysaccharide network protection strategy enhances photodynamic stability: Unlocking new applications of edible pigments in fruit preservation.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.163413]
19. Bingzhi Li, Yangyang Li, Yiya Ping, Liang Zhang, Linpin Luo, Yuechun Li, Wentao Zhang, Guangjun Huang, Jianlong Wang.  (2026)  Molecular interface engineering light-driven gellan gum antibacterial films with amplified photothermal-photocatalytic synergy for enhanced cherry tomato preservation.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.172489]
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