COMPARATIVE TABLE AgBB NIK/LCI list

Σχετικά έγγραφα
Universal Solvent GC Method Table

PROPERTIES OF COMMON LABORATORY SOLVENTS

Env-A 1400 Regulated Toxic Air Pollutant (RTAP) Analysis - STEP 1 - De Minimus Evaluation

Molecular Basis of Olfactory Chemoreception in the Common Bed Bug, Cimex lectularius. Feng Liu, Zhou Chen, Nannan Liu

Pankow JF, Luo W, Melnychenko AN, Barsanti, KC, Isabelle LM, Chen C, Guenther AB, Rosenstiel TN.

Supplementary Material for Statistical Field Theory for Polar Fluids

Supplementary Materials: Risk Assessment for Children Exposed to Beach Sands Impacted by Oil Spill Chemicals

Άρθρο 28 (1) Επιχρίσματα επιφανειών που προορίζονται να έλθουν σ επαφή με τρόφιμα.

Universal Solvation Model Based on Solute Electron Density. and on a Continuum Model of the Solvent Defined by

GC-MS 84.22% % Aroma components analysis in blackcurrant fruit and fruit wine by GC-MS

Chemical Name Index. Chemical Name Index 459

1. 2 PEN3 Portable Electronic Nose 3

Επιστήμη Υλικών ΙΙ (Θ) Α Ε Τ. Ενότητα 4 : Τριγωνικό Διάγραμμα Διαλυτότητας. Το νερό ως διαλύτης.

Comparison of experimental and estimated polarizabilities for organic compounds using ThermoML Archive data

SUPPLEMENTARY INFORMATION

20 C/68 F 60 C/140 F 100 C/212 F

ΠΑΝΕΠΙΣΤΗΜΙΟ ΘΕΣΣΑΛΙΑΣ

Chemical Name Index 443

ΠΑΡΑΡΤΗΜΑ Α - ΛΙΣΤΑ ΑΝΑΛΩΣΙΜΩΝ

In-Depth Aroma and Sensory Profiling of Unfamiliar Table- Grape Cultivars

Συγκεντρωτικόσ πίνακασ αςφμβατων μεταξφ τουσ χθμικών

REACH SIPA ACH BERTHIER Déc 08 - version 1

Global Reference List of Chemically Defined Substances

Sulfonated graphene as highly efficient and reusable acid carbocatalyst for the synthesis of ester plasticizers

Sound Speed & Pipe Size Data

MVOC. Damp Dampness WHO. Volatile Organic Compounds : VOC VOC. VOC MVOC : Microbial Volatile Organic Compounds MVOC MVOC MVOC MVOC .- -,.

ΠΑΝΕΠΙΣΤΗΜΟ ΘΕΣΣΑΛΙΑΣ ΣΧΟΛΗ ΓΕΩΠΟΝΙΚΩΝ ΕΠΙΣΤΗΜΩΝ ΤΜΗΜΑ ΓΕΩΠΟΝΙΑΣ ΙΧΘΥΟΛΟΓΙΑΣ ΚΑΙ ΥΔΑΤΙΝΟΥ ΠΕΡΙΒΑΛΛΟΝΤΟΣ

FINAR LIMITED. SAP Code CAS No. Item Description Packing HSN Code Price (INR) TAX RATE

15PROC

ΠΡΟΓΙΟΡΙΜΟ ΣΗ ΓΔΩΓΡΑΦΙΚΗ ΠΡΟΔΛΔΤΗ ΣΟΤ ΘΤΜΑΡΙΙΟΤ ΜΔΛΙΟΤ ΜΔ ΒΑΗ ΣΙ ΠΣΗΣΙΚΈ ΣΟΤ ΔΝΩΔΙ

ΕΝΕΡΓΟΣ ΦΥΤΙΚΟΣ ΑΝΘΡΑΚΑΣ

Analytical Chemistry

Ποιοτικά Χαρακτηριστικά Ελαιολάδου. Μαρία Τασιούλα-Μάργαρη. Τμήμα Χημείας Πανεπιστήμιο Ιωαννίνων

ELECTRONIC SUPPLEMENTARY MATERIAL. Figure 1S.- Chemical structure of: a) alizarin; b) purpurin; c) pseudopurpurin; d) xanthopurpurin; e) quinizarin.

Supplementary Material for Synthesis of Compact Multidentate Ligands to Prepare Stable Hydrophilic Quantum Dot Fluorophores

Επίσημη Εφημερίδα της Ευρωπαϊκής Ένωσης L 179/3

Orders may be placed by telephone, fax, or . Telephone orders are accepted Monday through Friday, between 9:00 a.m. and 5:00 p.m., Eastern Time.

Survey on specific PFCAs (C9-C20) and other fluorinated substances (precursors or similar substances) List of potential substances (examples)

1 h, , CaCl 2. pelamis) 58.1%, (Headspace solid -phase microextraction and gas chromatography -mass spectrometry,hs -SPME - Vol. 15 No.

LDPE : low density poly HDPE : high density. polyethylene terephthalate. GC AEDA aroma extract dilution assay PET +* ,* ppb.

Supporting Information: Design principles for α-tocopherol analogues

Συστατικά Προϊόντων Κωδικός Προϊόντος Περιγραφή Προϊόντος Συστατικά

Aluminium triflate as a Lewis acid catalyst for the ring opening of epoxides in alcohols

G4(MP2)-6X: A Cost-Effective Improvement to G4(MP2)

ΙΑΚΗΡΥΞΗ ΜΕΙΟ ΟΤΙΚΟΥ ΙΑΓΩΝΙΣΜΟΥ

ΜΑΘΕΤΕ ΠΕΡΙΣΣΟΤΕΡΑ ΠΟΛΥΑΙΘΥΛΕΝΙΟ (PE):

Eur. J. Org. Chem WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, 2006 ISSN X SUPPORTING INFORMATION

Supporting Information. for. Angew. Chem. Int. Ed. Z Wiley-VCH 2003

Ανάπτυξη βιοδιυλιστηρίων με χρήση ανανεώσιμων πρώτων υλών προς παραγωγή προϊόντων βιο-οικονομίας


Facile construction of the functionalized 4H-chromene via tandem. benzylation and cyclization. Jinmin Fan and Zhiyong Wang*

9. VOC & Μονάδες καύσης

REACH CERTIFICATE OF COMPLIANCE

Supplementary Figure S1. Single X-ray structure 3a at probability ellipsoids of 20%.

3 η ΕΝΟΤΗΤΑ, Μέρος 1 VOC και Μονάδες καύσης. Νίκος Ανδρίτσος

ΠΡΟΣΚΛΗΣΗ ΕΝΔΙΑΦΕΡΟΝΤΟΣ KAI ΚΑΤΑΘΕΣΗΣ ΠΡΟΣΦΟΡΩΝ

Supporting Information

Index of IFRA Standards 48 th Amendment

je; ^ T'/. Ti/iH im A τϋ ;α I'.'/: T: νθηγητησ ΘΕΟΑΩΡΙΛΗΣ Μ1ΧΑΛΗΣ ΣΤΕΣ ΜΑΛΛΙΑΧΟΒΑΣ ΑΠΟΣΤΟΑΟΣ ΒΟΪΤΣ1ΔΗΣ ΕΑΕΥΘΕΡ10Σ

Supporting Information. Copyright Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2007

Chemical profiling analysis of Maca using UHPLC-ESI-Orbitrap MS coupled. ingredients

PROMEX Pyriproxyfen 100 g/l EC

Elucidation of the Structure and Biological Activity of a New Sesquiterpene from Cistus creticus L.

Supporting Information

through induced intramolecularity

Supporting Information for Fe-Catalyzed Reductive Coupling of Unactivated Alkenes with. β-nitroalkenes. Contents. 1. General Information S2

Supporting Information

Kinds of Water Pollution. Inorganic Pollutants Organic Pollutants Biologic Pollutants

CONCENTRATIVE PROPERTIES OF AQUEOUS SOLUTIONS: DENSITY, REFRACTIVE INDEX, FREEZING POINT DEPRESSION, AND VISCOSITY

ArabRepublicofEgypt EDICTOFGOVERNMENT±

Supplementary Information

CRITICAL CONSTANTS. References

ΠΡΟΣΚΛΗΣΗ ΕΝΔΙΑΦΕΡΟΝΤΟΣ KAI ΚΑΤΑΘΕΣΗΣ ΠΡΟΣΦΟΡΩΝ ΓΙΑ ΤΗΝ ΑΝΑΘΕΣΗ ΤΗΣ ΠΡΟΜΗΘΕΙΑΣ

SPEKTRUM HASIL ANALISA GC-MS METIL ESTER

Synthesis of Imines from Amines in Aliphatic Alcohols on Pd/ZrO 2 Catalyst at Ambient Conditions

Copper-catalyzed formal O-H insertion reaction of α-diazo-1,3-dicarb- onyl compounds to carboxylic acids with the assistance of isocyanide

VII Contents Introduction Individual Fragrance and Flavor Materials

β-borylallylsilanes as a New Tool for Convenient Synthesis of Alkenylboranes

Παράδειγμα 4στ. Υπολογισμός Εναλλάκτη Κεροζίνης-Ακάθαρτου Πετρελαίου. Eίναι ο εναλλάκτης αυτός κατάλληλος για χρήση στην προκειμένη περίπτωση;

ΠΕΡΙΒΑΛΛΟΝ Ι. Βλυσίδη Απόστολου Καθηγητή ΕΜΠ

LATENT HEATS PHYSICAL AND CHEMICAL DATA

Supporting Information

AcO. O OAc OCH 3. Compound Number. (chloroform) Notes: M. Mozuch #36/46/Ac 21 mg. Acetone DMSO. CDCl 3. Atom

Copper-Catalyzed Oxidative Dehydrogenative N-N Bond. Formation for the Synthesis of N,N -Diarylindazol-3-ones

Asymmetric Synthesis of New Chiral β-amino Acid Derivatives by Mannich-type Reactions of Chiral N- Sulfinyl Imidates with N-Tosyl Aldimines

Supporting Information

Supplemental Materials

9. VOC & Μονάδες καύσης

Catalyst-free transformation of levulinic acid into pyrrolidinones with formic acid

Supporting Information-B. A Facile Iterative Synthesis of 2,5-Terpyrimidinylenes as Non-peptidic α-helical Mimics

cloquintocet-mexyl 1,2-benzisothiazol-3(2H)-one FENOVA SUPER CHEMINOVA A/S P.O. Box 9 DK-7620 Lemvig Denmark Xi;R38 R43 N;R51/53

POP ACRYLIC NAILS Ο ΗΓΙΕΣ ΧΡΗΣΗΣ

ΔΕΛΤΙΟ ΔΕΔΟΜΕΝΩN ΑΣΦΑΛΕΙΑΣ ΥΛΙΚΟΥ SAFEWASH 2000 JIGWASH

Metal-free Oxidative Coupling of Amines with Sodium Sulfinates: A Mild Access to Sulfonamides

Πρόσκληση υποβολής προσφοράς

Zuxiao Zhang, Xiaojun Tang and William R. Dolbier, Jr.* Department of Chemistry, University of Florida, Gainesville, FL

Optimization of (2,3-Dihydro-1-Benzofuran-3-yl)acetic Acids: Discovery of a Non-Free Fatty Acid-Like, Highly Bioavailable

Influence of Fuel Composition on the Emission of Oxygenated Pollutants (Organic Acids, Alcohols and Carbonyl Compounds) from a SI Engine

1.2 Χρήση της ουσίας/του παρασκευάσματος: Εμποτισμένο χαρτί με άρωμα σε συγκεκριμένο σχήμα, για τον αρωματισμό του εσωτερικού του αυτοκινήτου

Supporting Information. Experimental section

Transcript:

COMPARATIVE TABLE AgBB NIK/LCI list 2012 2015 AgBB- No CAS-No Name NIK NIK. AgBB AgBB 2012 2015 1 Aromatic hydrocarbons 1-1 108-88-3 Toluene 1900 2900 EU-LCI 1-2 100-41-4 Ethyl benzene 4400 850 EU-LCI 1-3 1330-20-7 Xylene, mix of o-, m- and p-xylene isomers 2200 500 EU-LCI 1-4 106-42-3 p-xylene 2200 500 EU-LCI 1-5 108-38-3 m-xylene 2200 500 EU-LCI 1-6 95-47-6 o-xylene 2200 500 EU-LCI 1-7 98-82-8 Isopropylbenzene (Cumene) 1000 500 1-8 103-65-1 n-propyl benzene 1000 950 EU-LCI 1-9 637-50-3 1-Propenyl benzene (ß-methyl styrene) 2400 2400 1-10 108-67-8 1.3.5-Trimethylbenzene 1000 450 EU-LCI 1-11 95-63-6 1.2.4-Trimethylbenzene 1000 450 EU-LCI 1-12 526-73-8 1.2.3-Trimethylbenzene 1000 450 EU-LCI 1-13 611-14-3 2-Ethyltoluene 1000 550 EU-LCI 1-14 527-84-4 1-Isopropyl-2-methylbenzene (o-cymene) 1100 1000 EU-LCI 1-15 535-77-3 1-Isopropyl-3-methylbenzene (m-cymene) 1100 1000 EU-LCI 1-16 99-87-6 1-Isopropyl-4-methylbenzene (p-cymene) 1100 1000 EU-LCI 1-17 95-93-2 1.2.4.5-Tetramethyl benzene 1100 500 EU-LCI 1-18 104-51-8 n-butyl benzene 1100 1100 EU-LCI 1-19 99-62-7 1.3-Diisopropylbenzene 1400 750 EU-LCI 1-20 100-18-5 1.4-Diisopropylbenzene 1400 750 EU-LCI 1-21 2189-60-8 Phenyl octane and isomers 1600 1100 EU-LCI 1-22 104-72-3 1-Phenyldecane and isomers 1800 1100 1-23 6742-54-7 1-Phenyl undecane and isomers 1900 1100 1-24 4994-16-5 4-Phenyl cyclohexene (4-PCH) 1300 300 1-25 100-42-5 Styrene 860 250 EU-LCI 1-26 536-74-3 Phenyl acetylene 840 200 1-27 98-83-9 2-Phenylpropene (α-methylstyrene) 2500 2500 1-28 25013-15-4 Vinyl toluene (all isomers: o-,m-,p-methyl styrenes) 4900 4900 1-29 Other alkylbenzenes, as long as indiv. isomers have not to be evaluated differently 1000 450 1-30 91-20-3 Naphthalene 5 5 1-31 95-13-6 Indene 450 450 EU-LCI 2 Saturated aliphatic hydrocarbons (n-, iso- and cyclo-) 2-1 96-14-0 3-methyl pentane VVOC 2-2 110-54-3 n-hexane 72 72 2-3 110-82-7 Cyclohexane 7000 6000 EU-LCI 2-4 108-87-2 Methyl cyclohexane 8100 8100 2-5

2-6 2-7 2-8 142-82-5 n-heptane 21000 21000 2-9 saturated aliphatic hydrocarbons C6 - C8 15000 15000 2-10 saturated aliphatic hydrocarbons C9 - C16 6000 6000 EU-LCI 2-11 saturated aliphatic hydrocarbons C17 - C 22 1000 SVOC 3 Terpenes 3-1 498-15-7 3-Carene 1500 1500 EU-LCI 3-2 80-56-8 α-pinene 1500 2500 EU-LCI 3-3 127-91-3 ß-Pinene 1500 1400 EU-LCI 3-4 138-86-3 Limonene 1500 5000 EU-LCI 3-5 Other terpene hydrocarbons 1500 1400 EU-LCI 4 Aliphatic alcohols (n-, iso-, cyclo) and dialkohole 4-1 64-17-5 Ethanol VVOC 4-2 71-23-8 1-propanol VVOC 4-3 67-63-0 2-propanol - VVOC 4-4 75-65-0 Tert-butanol, 2-methylpropanol-2 620 620 EU-LCI 4-5 78-83-1 2-Methyl-1-propanol 3100 3100 4-6 71-36-3 1-Butanol 3100 3000 EU-LCI 4-7 71-41-0 30899-19-5 94624-12-1 6032-29-7 584-02-1 137-32-6 Pentanol (all isomers) 730 730 EU-LCI 123-51-3 598-75-4 75-85-4 75-84-3 4-8 111-27-3 1-Hexanol 2100 2100 EU-LCI 4-9 108-93-0 Cyclohexanol 2100 2000 EU-LCI 4-10 104-76-7 2-Ethyl-1-hexanol 540 300 EU-LCI 4-11 111-87-5 1-Octanol 500 500 4-12 123-42-2 4-Hydroxy-4-methyl-pentane-2-on (diacetone alcohol) 960 960 EU-LCI 4-13 other C4 - C10 n- and sio alcohol alcohols 500 500 4-14 other C11 - C13 n- and iso- alcoholcs 500 500 4-15 105-08-8 1,4 cyclo hexa di menthol 1600 5 Aromatic alcohols 5-1 108-95-2 Phenol 10 10 5-2 128-37-0 Butylated hydroxytoluene 100 100 EU-LCI 5-3 100-51-6 Benzyl alcohol 440 440 EU-LCI 6 Glycols, Glycolethers 6-1 57-55-6 Propylene glycol (1,2-Dihydroxypropane) 2500 2500 6-2 107-21-1 Ethylene glycol (Ethandiol) 260 260 6-3 111-76-2 Ethylene glycol-monobutylether (2- butoxyethanol) 490 1100 EU-LCI 6-4 111-46-6 Diethylene glycol 440 440 EU-LCI 6-5 112-34-5 Diethylene glycol-monobutylether 670 670 EU-LCI 6-6 122-99-6 2-Phenoxyethanol 1100 1100 EU-LCI

6-7 96-49-1 Ethylene carbonate 370 370 6-8 107-98-2 Propylene glycol monomethyl ether (1- Methoxy-2-propanol) 3700 3700 6-9 25265-77-4 2.2.4-Trimethyl-1.3-pentane diol, monoisobutyrate (Texanol ) 600 600 EU-LCI 6-10 7397-62-8 Butyl glycolate 550 550 6-11 124-17-4 Diethylene glycol monomethyl ether acetate (2-(2-butoxyethoxy) ethyl acetate 850 850 EU-LCI 6-12 34590-94-8 Dipropylene glycol monomethyl ether 3100 3100 EU-LCI 6-13 109-86-4 Ethylene glycol monomethyl ether (2- Methoxyethanol 3 3 6-14 110-80-5 Ethylene glycol monoethyl ether (2- Ethoxyethanol) 8 8 6-15 2807-30-9 Ethylene glycol monoisopropyl ether (2- Propoxyethanol) 860 860 EU-LCI 6-16 109-59-1 Ethylene glycol isopropylether (2- Methylethoxyethanol) 220 220 EU-LCI 6-17 112-25-4 Ethylene glycol n-hexyl ether (2- Hexoxyethanol) 1200 1400 6-18 110-71-4 1,2-Dimethoxyethan 4 4 6-19 629-14-1 1,2-Diethoxyethane 10 10 6-20 110-49-6 Ethylene glycol monomethyl ether acetate (2-Methoxyethyl acetate) 5 5 6-21 111-15-9 Ethylene glycol monoethyl ether acetate (2- Ethoxyethyl acetat) 11 11 6-22 112-07-2 Ethylenglykolbutyletheracetat (2-Butoxyethyl acetate) 1300 1300 6-23 112-59-4 Diethylene glycol n-hexyl ether (2-(2- Hexoxyethoxy)-ethanol) 740 740 6-24 111-96-6 Diethylene glycol dimethyl ether( 1- Methoxy-2-(2-methoxy-ethoxy)-ethan) 28 28 EU-LCI 6-25 1589-47-5 1-Propylene glycol 2-methyl ether (2- Methoxy-1-propanol) 19 19 EU-LCI 6-26 70657-70-4 1-Propylene glycol 2-methyl ether acetate (2-Methoxy-1-propyl acetate) 28 28 EU-LCI 6-27 623-84-7 Propylene glycol diacetat 5300 5300 6-28 110-98-5; 25265-71-8 Dipropylene glycol 670 670 EU-LCI 6-29 88917-22-0 Dipropylene glycol-monomethyl ether acetate 3900 3900 6-30 29911-27-1 Dipropylene glycol-mono-n-propylether 740 740 6-31 29911-28-2 35884-42-5 Dipropylene glycol-mono-n-butylether 810 810 6-32 132739-31-2 (mix) Dipropylene glycol-mono-t-butylether 810 810 6-33 110-63-4 1,4-Butylene glycol (1,4-Butandiol) 2000 2000 EU-LCI 6-34 20324-33-8 25498-49-1 Tripropylene glycol-mono-methylether 1200 2000 6-35 112-49-2 Triethylene glycol-dimethyl ether 7 7 6-36 7778-85-0 1.2.-Propylene glycol-dimethyl ether 25 25 6-37 6846-50-0 2,2,4-Trimethylpentanediol diisobutyrate (TXIB) 450 450 EU-LCI 6-38 111-90-0 Diethylene glycol monoethyl ether (2-(2- ethoxyethoxy)ethanol) 350 350 EU-LCI 6-39 63019-84-1 89399-28-0 Dipropylene glycol dimethyl ether 1300 1300 EU-LCI 111109-77-4 6-40 108-32-7 Propylene carbonate 250 250 6-41 107-41-5 Hexylene glycol (2-methyl-2,4-pentanediol) 490 490

6-42 2517-43-3 3-Methoxy-1-butanol 500 500 6-43 1569-01-3 30136-13-1 1,2-Propylene glycol n-propylether 1400 1400 6-44 5131-66-8 29387-86-8 15821-83-7 1,2-Propylene glycol n-butylether 1600 1600 63716-40-5 6-45 104-68-7 Diethylene glycol phenylether 1450 1450 6-46 126-30-7 Neopentyl glycol 1000 1000 7 Aldehyde 7-1 123-72-8 Butanal 650 VVOC/ EU-LCI 7-2 110-62-3 Pentanal 1700 800 EU-LCI 7-3 66-25-1 Hexanal 890 900 EU-LCI 7-4 111-71-7 Heptanal 1000 900 EU-LCI 7-5 123-05-7 2-Ethyl-hexanal 1100 900 EU-LCI 7-6 124-13-0 Octanal 1100 900 EU-LCI 7-7 124-19-6 Nonanal 1300 900 EU-LCI 7-8 112-31-2 Decanal 1400 900 EU-LCI 7-9 4170-30-3 123-73-9 2-Butenal (Crotonaldehyd, cis-trans-mix) 1 1 15798-64-8 7-10 1576-87-0 764-39-6 2-Pentenal 12 12 31424-04-1 7-11 6728-26-3 505-57-7 16635-54-4 2-Hexenal 14 14 1335-39-3 7-12 2463-63-0 18829-55-5 2-Heptenal 16 16 29381-66-6 7-13 2363-89-5 2548-87-0 25447-69-2 2-Octenal 18 18 20664-46-4 7-14 2463-538 18829-56-6 60784-31-8 2-Nonenal 20 20 30551-15-6 7-15 3913-71-1 2497-25-8 2-Decenal 22 22 3913-81-3 7-16 2463-77-6 53448-07-0 2-Undecenal 24 24 7-17 98-01-1 Furfural 20 20 7-18 111-30-8 Glutaraldehyde 2 2 7-19 100-52-7 Benzaldehyde 90 90 7-20 75-07-0 Acetaldehyde 1200 VVOC / EU-LCI 7-21 123-38-6 Propanal VVOC 7-22 50-00-0 Formaldehyde 100 VVOC 8 Ketones 8-1 78-93-3 Ethylmethylketone 6000 5000 EU-LCI 8-2 563-80-4 3-Methylbutanone-2 7000 7000 EU-LCI 8-3 108-10-1 Methylisobutylketone 830 830 8-4 120-92-3 Cyclopentanone 900 900 EU-LCI 8-5 108-94-1 Cyclohexanone 410 410 EU-LCI

8-6 1120-72-5 2-Methylcyclopentanone 1000 1000 8-7 583-60-8 2-Methylcyclohexanone 2300 2300 EU-LCI 8-8 98-86-2 Acetophenone 490 490 EU-LCI 8-9 116-09-6 1-Hydroxyacetone (2 Propanone, 1- hydrocx-) 2400 2400 8-10 67-64-1 Aceton 1200 VVOC 9 Acids 9-1 64-19-7 Acetic acid 1250 1250 9-2 79-09-4 Propionic acid 310 310 EU-LCI 9-3 79-31-2 Isobutyric acid 370 370 9-4 107-92-6 Butyric acid 370 370 9-5 75-98-9 2,2-Dimethylpropanoic acid (pivalic acid) 420 420 9-6 109-52-4 n-pentanoic acid (n-valeric acid) 420 420 9-7 142-62-1 n-hexanoic acid (n-caproic acid) 490 490 9-8 111-14-8 n-heptanoic acid 550 550 9-9 124-07-2 n-octanoic acid 600 600 9-10 149-57-5 2-Ethylhexanoic acid 50 150 10 Esters 10-1 79-20-9 Methyl acetate VVOC 10-2 141-78-6 Ethyl acetate VVOC 10-3 108-05-4 Vinyl acetate VVOC 10-4 108-21-4 Isopropyl acetate 4200 4200 EU-LCI 10-5 109-60-4 Propyl acetate 4200 4200 EU-LCI 10-6 108-65-6 2-Methoxy-1-methylethyl acetate 2700 2700 EU-LCI 10-7 592-84-7 n butyl acetate 2000 2000 10-8 80-62-6 Methyl methacrylate 2100 2100 10-9 Other methacrylates 2100 2100 10-10 110-19-0 Isobutyl acetate 4800 4800 EU-LCI 10-11 123-86-4 1 Butyl acetate 4800 4800 EU-LCI 10-12 103-09-3 2-Ethylhexyl acetate 690 350 10-13 96-33-3 Methyl acrylate 180 180 EU-LCI 10-14 140-88-5 Ethyl acrylate 210 210 EU-LCI 10-15 141-32-2 n-butyl acrylate 110 110 EU-LCI 10-16 103-11-7 2-Ethylhexyl acrylate 380 380 EU-LCI 10-17 Other acrylates (acrylic acid esters) 110 110 EU-LCI 10-18 627-93-0 Dimethyl adipate 50 50 EU-LCI 10-19 105-75-9 Dibutyl fumarate 50 50 EU-LCI 10-20 106-65-0 Dimethyl succinate 50 50 EU-LCI 10-21 1119-40-0 Dimethyl glutarate 50 50 EU-LCI 10-22 13048-33-4 Hexamethylene diacrylate 10 10 EU-LCI 10-23 105-76-0 Maleic acid dibutylester 50 50 EU-LCI 10-24 96-48-0 Butyrolactone 2700 2700 10-25 71195-64-7 Diisobutyl glutarate 100 100 10-26 925-06-4 Diisobutyl succinate 100 100 11 Chlorinated hydrocarbons not in use at the moment

12 Others 12-1 123-91-1 1.4-Dioxan 73 73 12-2 105-60-2 Caprolactam 240 300 EU-LCI 12-3 872-50-4 N-methyl-2-pyrrolidon 400 400 12-4 556-67-2 Octamethylcyclotetra-siloxane (D4) 1200 1200 EU-LCI 12-5 100-97-0 Hexamethylenetetramine 30 30 EU-LCI 12-6 96-29-7 2-Butanonoxime 20 20 12-7 126-73-8 Tributyl phosphate SVOC 12-8 78-40-0 Triethyl phosphate 75 75 12-9 26172-55-4 5-Chloro-2-methyl-2H-isothiazol-3-one (CIT) 1 1 EU-LCI 12-10 2682-20-4 2-Methyl-4-isothiazolin-3-one 100 100 EU-LCI 12-11 121-44-8 Triethylamine 42 42 12-12 541-02-6 Decamethylcyclopentasiloxane (D5) 1500 1500 12-13 540-97-6 Dodecamethylcyclohexa-siloxane (D6) 1200 1200 12-14 109-99-9 Tetrahydrofuran 1500 1500 12-15 68-12-2 Dimethylformamide 15 15 12-16 107-50-6 Tetradeca methyl cyclo heptasiloxane (D7) 1200 12-17 2687-91-4 n ethyl 2 pyrrolidon 430 Explanations to colours in column 2015: RED new or (sharpened) change to version 2012 BLACK no change to before GREEN mitigated to version 2012 Where the value of version 2015 has been harmonised with EU-LCI it is stated.