Bentonite BA - 03

KERAMOST, a.s

Revision date : 2021-05-17

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Health risk rating 1
Safety risk rating 1
Environmental risk rating 1

Note: Ingredients listed on restricted chemical lists

EC/CAS

1302-78-9

Name of the chemical

bentonite

Concentration

N/A

General Information

Revision date

2021-05-17

Product name

Bentonite BA - 03

CAS No.

1302-78-9

REACH No

Exempted

1.2.1 Relevant identified uses

Bentonite can be used as a rheology modifier, adsorbent, filler and for water purification (filtration) or ecological application

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Company Information

company name

KERAMOST, a.s

e-mail address of the competent person responsible for the Safety Data Sheet

reach@keramost.cz

Section 2

2.1 Classification of the substance or mixture

Depending on the handling and use (grinding, drying, bagging), airborne respirable dust may be generated. Dust contains respirable crystalline silica. Prolonged and or massive inhalation of respirable crystalline silica dust may cause lung fibrosis, commonly referred to as silicosis. Principal symptoms of silicosis are cough and breathlessness. Occupational exposure to respirable dust should be monitored and controlled. The product should be handled using methods and techniques that minimize or eliminate dust generation. The product contains less than 1% w/w RCS (respirable crystalline silica) as determined by the SWERF method. The respirable crystalline silica content can be measured using the “Size-Weighted Respirable Fraction – SWERF” method. All details about the SWERF method is available at www.crystallinesilica.eu. Regulation EC 1907/2006 (REACH) Not classified – is not hazardous substance. Regulation EC 1272/2008 (CLP) Doesn’t meet the criteria for classification. Directive 67/548/EEC It is not classified as a dangerous substance or mixture.

2.2 Label elements

Not applicable – not required.

2.3 Other hazards

Inorganic material of natural origin. The substance does not meet the criteria for PBT or vPvB substance. No other hazards identified. Bentonite is not known to have an adverse effect on the endocrine system in accordance with the criteria stated within Regulation (EU) 2017/2100 or Regulation (EU) 2018/605.

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