Eco-labelling: legal, decent, honest and truthful?
Literature Information
The first page of this article is displayed as the abstract.
Related Literature
Sulfur antisite-induced intrinsic high-temperature ferromagnetism in Ag2S:Y nanocrystals
Pan Wang, Tianye Yang, Rui Zhao, Mingzhe Zhang
DOI: 10.1039/C5CP07690K
Degradation behavior and biosafety studies of the mPEG–PLGA–PLL copolymer
Ying Sun, Jun Cao, Yourong Duan
DOI: 10.1039/C6CP00767H
Insights into the reaction mechanism of 3-O-sulfotransferase through QM/MM calculations
Rui P. Sousa, Pedro A. Fernandes, Maria J. Ramos, Natércia F. Brás
DOI: 10.1039/C5CP06224A
Photo-induced oxidation of the uniquely liganded heme f in the cytochrome b6f complex of oxygenic photosynthesis
Adrien A. P. Chauvet, Rachna Agarwal, André al Haddad, Frank van Mourik, William A. Cramer
DOI: 10.1039/C6CP01592A
A DFT-based comparative equilibrium study of thermal dehydration and hydrolysis of CaCl2 hydrates and MgCl2 hydrates for seasonal heat storage
Amar Deep Pathak, Silvia Nedea, Herbert Zondag, Camilo Rindt, David Smeulders
DOI: 10.1039/C6CP00926C
Remarkable enhancement in the Kapitza resistance and electron potential barrier of chemically modified In2O3(ZnO)9 natural superlattice interfaces
DOI: 10.1039/C5CP05076F
Density functional investigation and some optical experiments on dye-sensitized quantum dots
Kalpna Jain, Sreejith Kaniyankandy, Shyam Kishor, Ida Josefsson, Hirendra N. Ghosh, Khundrakpam S. Singh, Sumit Mookerjee, Michael Odelius, Lavanya M. Ramaniah
DOI: 10.1039/C5CP03816B
Geometry controlled anomalous diffusion in random fractal geometries: looking beyond the infinite cluster
DOI: 10.1039/C5CP03548A
Quantum chemical protocols for modeling reactions and spectra in astrophysical ice analogs: the challenging case of the C+ + H2O reaction in icy grain mantles
DOI: 10.1039/C5CP03393D
Interfacial charge-transfer transitions in a TiO2-benzenedithiol complex with Ti–S–C linkages
Jun-ichi Fujisawa, Ryuki Muroga, Minoru Hanaya
DOI: 10.1039/C5CP05046D
You might also like
What are the main uses of (3.beta.)-3-Hydroxy-N,N-dimethyl-chol-5-en-24-amide (CAS: 79066-03-8)?
(3.beta.)-3-Hydroxy-N,N-dimethyl-chol-5-en-24-amide (CAS: 79066-03-8) is primari...
What regulatory guidelines apply to 5-(aminomethyl)-2-methoxyphenol (CAS: 89702-89-6)?
5-(Aminomethyl)-2-methoxyphenol (CAS: 89702-89-6) is classified under GHS as a s...
What is Thieno[2,3-c]pyridin-7(6H)-one (CAS: 28981-13-7)?
Thieno[2,3-c]pyridin-7(6H)-one (CAS: 28981-13-7) is a heterocyclic organic compo...
Is 1-[(6-Methoxy-3-pyridinyl)methyl]-4-piperidinamine dihydrochloride (CAS: 1185311-28-7) safe?
1-[(6-Methoxy-3-pyridinyl)methyl]-4-piperidinamine dihydrochloride is generally ...
What regulatory guidelines apply to [(2E)-3-Phenyl-2-propen-1-yl]phosphonic acid (CAS: 146404-58-2)?
[(2E)-3-Phenyl-2-propen-1-yl]phosphonic acid (CAS: 146404-58-2) is regulated und...
What regulatory guidelines apply to 6-Bromo-7-methoxyquinoline (CAS: 1620515-86-7)?
6-Bromo-7-methoxyquinoline (CAS: 1620515-86-7) falls under the scope of the Glob...
What industries use (2R)-1-(1-Benzofuran-2-yl)-N-propyl-2-pentanamine (CAS: 260550-89-8)?
This compound is primarily used in the pharmaceutical industry for the developme...
What are the main uses of 1-Ethyl-7-[2-methyl-6-(4H-1,2,4-triazol-3-yl)-3-pyridinyl]-3,5-dihydropyrazino[2,3-b]pyrazin-2(1H)-one (CAS: 1228013-15-7)?
1-Ethyl-7-[2-methyl-6-(4H-1,2,4-triazol-3-yl)-3-pyridinyl]-3,5-dihydropyrazino[2...
Are there alternatives to {5-(Acryloylamino)-2-[(dimethylamino)methyl]phenyl}boronic acid (CAS: 1217500-78-1) in synthesis?
Alternative reagents such as 2-[(dimethylamino)methyl]phenylboronic acid or rela...
What is 3-(Piperidin-4-yloxy)pyridine (CAS: 310881-48-2)?
3-(Piperidin-4-yloxy)pyridine (CAS: 310881-48-2) is an organic compound with the...
Source Journal
Green Chemistry

Green Chemistry provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on, but not limited to, the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998). Green chemistry is the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry is at the frontiers of this continuously-evolving interdisciplinary science and publishes research that attempts to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. Submissions on all aspects of research relating to the endeavour are welcome. The journal publishes original and significant cutting-edge research that is likely to be of wide general appeal. To be published, work must present a significant advance in green chemistry. Papers must contain a comparison with existing methods and demonstrate advantages over those methods before publication can be considered. For more information please see this Editorial. Coverage includes the following, but is not limited to: Design (e.g. biomimicry, design for degradation/recycling/reduced toxicity…) Reagents & Feedstocks (e.g. renewables, CO2, solvents, auxiliary agents, waste utilization…) Synthesis (e.g. organic, inorganic, synthetic biology…) Catalysis (e.g. homogeneous, heterogeneous, enzyme, whole cell…) Process (e.g. process design, intensification, separations, recycling, efficiency…) Energy (e.g. renewable energy, fuels, photovoltaics, fuel cells, energy storage, energy carriers…) Applications (e.g. electronics, dyes, consumer products, coatings, pharmaceuticals, preservatives, building materials, chemicals for industry/agriculture/mining…) Impact (e.g. safety, metrics, LCA, sustainability, (eco)toxicology…) Green chemistry is, by definition, a continuously-evolving frontier. Therefore, the inclusion of a particular material or technology does not, of itself, guarantee that a paper is suitable for the journal. To be suitable, the novel advance should have the potential for reduced environmental impact relative to the state of the art. Green Chemistry does not normally deal with research associated with 'end-of-pipe' or remediation issues.














