Chlorophyllin sodium copper salt - 10mM in Water , CAS No.11006-34-1

CAS: 11006-34-1 Cat. No.: C420584 Molecular Weight: 724.15 EC Number: 234-242-5 PubChem CID: 23725082
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GRADE & PURITY 10mM in Water
Synonyms
Chlorophyllins|EINECS 287-483-3|85536-03-4|Chlorophyllin sodium copper salt|copper;trisodium;3-[20-(carboxylatomethyl)-18-(dioxidomethylidene)-8-ethenyl-13-ethyl-3,7,12,17-tetramethyl-2,3-dihydroporphyrin-23-id-2-yl]propanoate|DTXSID1045956|Derifil (TN)|S
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1ml
C420584-1ml
2
$49.90
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Why this grade

10mM in Water for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs 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.

Overview

Chlorophyllin sodium copper salt has been used to study the effect of chlorophyllin against radiation-induced hematopoietic syndrome.It has been used to study the effect of chlorophyllin on the excretion of PhIP (2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine) and its metabolites into the breast-milk of lactating rats.

Specifications

Synonyms
Chlorophyllins | EINECS 287-483-3 | 85536-03-4 | Chlorophyllin sodium copper salt | copper;trisodium;3-[20-(carboxylatomethyl)-18-(dioxidomethylidene)-8-ethenyl-13-ethyl-3, 7, 12, 17-tetramethyl-2, 3-dihydroporphyrin-23-id-2-yl]propanoate | DTXSID1045956 | Derifil (TN) | S
Specifications & Purity
10mM in Water
Biochemical and Physiological Mechanisms
Antioxidant, antimutagenic agent. Shows antimutagenic effects against a range of mutagenic agents but potentiates the mutagenic effects of alkylating agents. Shows antiproliferative effects. Chlorophyll a- and b-derivative. Shows antioxidant effects in vi
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers
Isomeric SMILES CCC1=C(C2=CC3=NC(=CC4=NC(=C(C5=NC(=C(C5=C([O-])[O-])C)C=C1[N-]2)CC(=O)[O-])C(C4C)CCC(=O)[O-])C(=C3C=C)C)C.[Na+].[Na+].[Na+].[Cu+2]
WGK Germany 2
RTECS GS2168866
PubChem CID 23725082
Molecular Weight 724.15

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

Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
SensitivityLight sensitive.
Molecular Weight724.100 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count10
Rotatable Bond Count5
Exact Mass723.123 Da
Monoisotopic Mass723.123 Da
Topological Polar Surface Area164.000 Ų
Heavy Atom Count48
Formal Charge0
Complexity1750.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count2
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count5
Documents & Articles
Citations of This Product
References
1. Shuangshou Wang, Lu Zhang, Qiwen Jin, Zhongqiu Xu, Jiayi Zhao, Yuwen Ding, Wenzhi Li, Peng Lin, Jing Gu, Qi Zhang, Yang Chen, Hongmei Chen, Tingxuan Yan.  (2022)  Filter paper-based colorimetric analysis: An instrument-free strategy for semiquantitative naked-eye detection of food colorants.  FOOD CHEMISTRY,      [PMID:35551021] [10.1016/j.foodchem.2022.133087]
2. Shibo Sun, Yici Zhang, Weiping Xu, Yue Zhang, Rui Yang, Jianli Guo, Shui Guan, Qiang Ma, Kun Ma, Jianqiang Xu.  (2021)  Chlorophyllin Inhibits Mammalian Thioredoxin Reductase 1 and Triggers Cancer Cell Death.  Antioxidants,  10  (11): (1733).  [PMID:34829604] [10.3390/antiox10111733]
3. Zhen Lin, Linlin Zheng, Wensong Yao, Shijun Liu, Yemei Bu, Qi Zeng, Xiaomin Zhang, Haohua Deng, Xinhua Lin, Wei Chen.  (2020)  A facile route for constructing Cu–N–C peroxidase mimics.  Journal of Materials Chemistry B,  (37): (8599-8606).  [PMID:32820298] [10.1039/D0TB01494J]
4. 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]
5. Changping Xu, Yangyuan Zhang, Yangbo Bai, Yinping Miao.  (2024)  Highly sensitive Fabry–Perot sensor for the detection of sodium copper chlorophyllin.  OPTICS AND LASER TECHNOLOGY,      [PMID:] [10.1016/j.optlastec.2024.111483]
6. Shuwei Zhou, Qiong Wu, Qiaoxia Wang, Hong Fu, Fang Yang.  (2024)  Assembly of primary secondary amine over magnetic graphitized carbon black material for selective cleansing of sample matrices.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2024.111365]
7. Tianjiao Liu, Deming Dong, Yingyi Meng, Haijun Chen, Chunyue Liu, Zihan Qi, Anfeng Li, Yang Ning.  (2024)  Facile and green synthesis of chlorophyll-derived multi-color fluorescent carbonized polymer dots and their use for sensitive detection of hemin.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:38241933] [10.1016/j.saa.2024.123841]
8. Duan Peng, Wang Chenxing, Huang Yinpeng, Fu Chunqiao, Lu Xulei, Zhang Yong, Yao Yuming, Chen Lei, He Qi-Chang, Qian Linmao, Yang Tingting.  (2025)  Moisture-based green energy harvesting over 600 hours via photocatalysis-enhanced hydrovoltaic effect.  Nature Communications,  16  (1): (1-10).  [PMID:39747063] [10.1038/s41467-024-55516-z]
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