EU harmonized hazard classification, hazard statements, pictograms, and signal word.
SOURCEEU CLP Annex VI (ECHA)1 classifications
Hazard Class
H-Statements
Pictograms
Signal
Repr. 2; Acute Tox. 3 *; Skin Sens. 1
H361f ***; H301; H317
GHS08; GHS06
Danger
ICSC Chemical Safety
International Chemical Safety Card hazard and exposure summary.
SOURCEWHO/JECFA1 records
Field
Value
GHS Signal Word
DANGER
GHS Hazard Statements
Toxic if swallowed Causes mild skin irritation Causes eye irritation May cause allergic skin reaction Suspected of damaging fertility or the unborn child Harmful to aquatic life
Short-term Effects
The substance is irritating to the eyes and skin.
Long-term Effects
Repeated or prolonged contact may cause skin sensitization. Animal tests show that this substance possibly causes toxicity to human reproduction or development.
Routes of Exposure
The substance can be absorbed into the body in hazardous amounts by ingestion. The substance can be absorbed into the body through the skin.
Functional Uses
Industrial and product-use categories associated with this substance.
SOURCEEPA CPDat2 records
Preservative
Regulatory Lists
Inventory, screening, and regulatory list matches from public chemical databases.
SOURCEEPA CPDat4 records
List
Keyword
Source
active_ingredient; Europe; Pesticides
Commission of the European Communities
CPCat
Indirect additives food contact (10/2018)
FDA
United States Food and Drug Administration (FDA)
banned; Europe; Personal care
European Commission
CosIng
Europe; Personal care
European Commission
CosIng
NOAEL Studies
Toxicology endpoints rendered from public NOAEL study rows.
SOURCENOAEL studiesShowing 50 of 59 studies
Value
Unit
Endpoint
Route
Species
Source
10
mg/kg bw/d
-
intravenous
rabbit
Regulatory source
10
mg/kg bw/day
-
oral
rat
Regulatory source
10
mg/kg bw/d
-
oral
rat
Regulatory source
20
-
-
oral
rabbit
Regulatory source
40
%
-
oral
rabbit
Regulatory source
50
mg/kg bw/ d
-
dermal
rat
Regulatory source
0.07979
%
Concentration, 5% incidence of positive responses
Dermal
Human
NTP ICE skin sensitization
0.3661
%
Concentration, 5% incidence of positive responses
Dermal
Human
NTP ICE skin sensitization
0.01064
%
Concentration, one positive response
Dermal
Human
NTP ICE skin sensitization
0.03571
%
Concentration, one positive response
Dermal
Human
NTP ICE skin sensitization
=0.705
mg/m3
DNEL systemic
inhalation
Human
ToxValDB GESTIS DNEL
2R97846T1L
UNII
FDA UNII substance identifier
-
-
openFDA substances
17.07
%
Incidence of positive responses
Dermal
Human
NTP ICE skin sensitization
31.33
%
Incidence of positive responses
Dermal
Human
NTP ICE skin sensitization
625
ug/cm2
Induction dose per skin area
Dermal
Human
NTP ICE skin sensitization
968.8
ug/cm2
Induction dose per skin area
Dermal
Human
NTP ICE skin sensitization
99.73
ug/cm2
Induction dose per skin area, 5% incidence of positive responses
Dermal
Human
NTP ICE skin sensitization
283.7
ug/cm2
Induction dose per skin area, 5% incidence of positive responses
Dermal
Human
NTP ICE skin sensitization
13.3
ug/cm2
Induction dose per skin area, one positive response
Dermal
Human
NTP ICE skin sensitization
27.68
ug/cm2
Induction dose per skin area, one positive response
Dermal
Human
NTP ICE skin sensitization
=70
mg/kg bw
LD50
oral
Rat
NTP ICE acute oral
=138
mg/kg bw
LD50
oral
Rat
NTP ICE acute oral
=275
mg/kg bw
LD50
oral
Rat
NTP ICE acute oral
=290
mg/kg bw
LD50
oral
Rat
NTP ICE acute oral
=306
mg/kg bw
LD50
oral
Rat
NTP ICE acute oral
=221
mg/kg bw/day
LEL
oral
Rat
ECHA
=222
mg/kg bw/day
LEL
oral
Rat
ECHA
=225
mg/kg bw/day
LEL
oral
Rat
ECHA
=341
mg/kg bw/day
LEL
oral
Rat
ECHA
=382
mg/kg bw/day
LEL
oral
Rat
ECHA
=417
mg/kg bw/day
LEL
oral
Rat
ECHA
=3
mg/kg bw/d
NOAEL
-
-
SCCS Opinion
=9.6
mg/kg bw/day
NOAEL
oral
Rat
ECHA
=10
mg/kg bw/day
NOAEL
oral
Rat
ECHA
=10
mg/kg bw/d
NOAEL
intravenous
rabbit
SCCS Opinion
=10
mg/kg bw/day
NOAEL
oral
rat
SCCS Opinion
<12.5
mg/kg bw/day
NOAEL
oral
Rat
ECHA
=16.6
mg/kg bw/d
NOAEL
oral
rat
SCCS Opinion
=20
-
NOAEL
oral
rabbit
SCCS Opinion
=24
mg/kg bw/d
NOAEL
-
-
SCCS Opinion
=35
mg/kg
NOAEL
oral
-
SCCS Opinion
=40
%
NOAEL
oral
rabbit
SCCS Opinion
=50
mg/kg bw/day
NOAEL
dermal
Rat
ECHA
=50
mg/kg bw/d
NOAEL
dermal
-
SCCS Opinion
=50
mg/kg bw/ d
NOAEL
dermal
rat
SCCS Opinion
=100
ppm
NOAEL
oral
Rat
ECHA
3
unitless
Relative reliability score
Dermal
Human
NTP ICE skin sensitization
50
mg/kg bw/d
dermal absorption
dermal
-
Regulatory source
50
mg/kg bw/d
dermal absorption
dermal
rabbit
Regulatory source
10
mg/kg bw/d
genotoxicity
oral
-
Regulatory source
Showing 50 of 59 studies
REACH Registration
Registration status from the ECHA REACH registered substances database.
EU Scientific Committee opinions tied to the matched substance.
SOURCESCCS Opinion2 opinions
Opinion
Date
Conclusion
Max Conc.
Concerns
SCCS/1432/11
22 March 2011
Not safe — not safe under current use conditions
Not safe at 0.3% (current permitted level)
Genotoxicity potential; skin sensitization; insufficient margin of safety at authorised level
SCCS/1360/10
2011-03-22
On the basis of the data available, the SCCS comes to the conclusion that 2-chloroacetamide is not safe for consumers when used under the current use conditions of 0.3% in cosmetic products. Human data demonstrate that allergic reactions can be elicited at concentrations lower than 0.3% (use conditions in cosmetics products).
0.3%
Human data demonstrate allergic (sensitising) reactions can be elicited at concentrations lower than the 0.3% in-use level; classified Repr. Cat 3, Acute Tox 3, Skin Sens 1.
Cosmetic Safety Profile
Same-CAS cosmetic ingredient record for cross-vertical context.
What is the GHS hazard classification for Chloroacetamide?
Chloroacetamide (CAS 79-07-2) is classified under EU CLP Annex VI as Repr. 2; Acute Tox. 3 *; Skin Sens. 1 with signal word Danger. Hazard statements: H361f ***; H301; H317. Source: EU CLP Annex VI (ECHA).
What is the NOAEL for Chloroacetamide?
Chloroacetamide has 59 NOAEL studies in the database. The lowest reported value is 0.01064 % via Dermal in Human. Source: NTP ICE skin sensitization.
What regulatory lists include Chloroacetamide?
Chloroacetamide appears on 4 regulatory/inventory lists including active_ingredient; Europe; Pesticides, Indirect additives food contact (10/2018), banned; Europe; Personal care, and 1 more. Source: EPA CPDat.
Is Chloroacetamide used in cosmetics?
Yes, Chloroacetamide is also indexed as a cosmetic ingredient under the name Chloroacetamide. View the full cosmetic safety profile on the ingredient page for detailed safety data, SCCS opinions, and regulatory status.
Where does the safety data for Chloroacetamide come from?
Safety data is sourced from ECHA CLP Annex VI, EPA ToxValDB, EPA CPDat, EPA DSSTox, ECHA REACH, ILO/WHO ICSC, CosIng / Ingredients DB, ChEMBL / DailyMed. All data traces to primary regulatory sources and is updated from official government databases.
Does Chloroacetamide have different safety status in cosmetics vs industrial chemicals?
Chloroacetamide is prohibited in EU cosmetics but has active industrial GHS classifications (H361f, H301, H317).
Is Chloroacetamide used outside industrial chemicals?
Chloroacetamide also appears in cosmetics, pharmaceutical databases.