Note: Ingredients listed on restricted chemical lists
EC/CAS
247-761-7/26530-20-1
Name of the chemical
2-Octyl-2H-isothiazol-3-one
Concentration
<4
General Information
Version
1.1
Revision date
2024-03-01
Product name
ULTRATILE PG FLOWABLE GROUT SILVER GREY
1.2.1 Relevant identified uses
Consumer use,Industrial use,Professional use
Emergency telephone
+44 (0)7971 217 347
Icons in SDS
Company Information
company name
Instarmac PLC
e-mail address of the competent person responsible for the Safety Data Sheet
email@instarmac.co.uk
GHS Information
Signal word
Warning
Hazard Codes
Hazard statements (CLP)
H317, H412
Hazard statements
Code
Statements
H317
May cause an allergic skin reaction
Section 2
SECTION 2: Hazards identification
Adverse physicochemical, human health and environmental effects
May cause an allergic skin reaction. Harmful to aquatic life with long lasting effects.
2.2 Label elements
Labelling
Hazard pictograms
GHS07
Signal word
Warning
Contains
octhilinone (ISO); 2-octyl-2H-isothiazol-3-one
Hazard statements
H317 - May cause an allergic skin reaction. H412 - Harmful to aquatic life with long lasting effects.
Precautionary statements
P261 - Avoid breathing dust/fume/gas/mist/vapours/spray. P272 - Contaminated work clothing should not be allowed out of the workplace. P273 - Avoid release to the environment. P280 - Wear protective gloves/protective clothing/eye protection/face protection/hearing protection. P302+P352 - IF ON SKIN: Wash with plenty of water. P321 - Specific treatment (see supplemental first aid instruction on this label).
Other hazards which do not result in classification
Product contains chromate reducing agent. Therefore, the cement/binder contains less than 0,0002% of water-soluble Chromium(VI). If the storage conditions are not appropriate (exposure to humidity) or the storage period is exceeded, the effectiveness of the present reducing agent can be diminished prematurely, and the cement/binder can become skin sensitizing (H317 or EUH203, respectively). Contains no PBT and/or vPvB substances ≥ 0.1% assessed in accordance with REACH Annex XIII The mixture does not contain substance(s) included in the list established in accordance with Article 59(1) of REACH for having endocrine disrupting properties, or substance(s) are not identified as having endocrine disrupting properties in accordance with the criteria set out in Commission Delegated Regulation (EU) 2017/2100 or Commission Regulation (EU) 2018/605 at a concentration equal to or greater than 0,1 %