NOAEL Data IARC Group 3 REACH Registered Cosmetic Ingredient

Bis(2-ethylhexyl)hexanedioate

Also known as: Adimoll DO, DEHA, Hexanedioic acid, bis(2-ethylhexyl) ester, Adipic acid, bis(2-ethylhexyl) ester, BRN 1803774 (+15 more)

CAS 103-23-1

Bis(2-ethylhexyl)hexanedioate (CAS 103-23-1) is a chemical substance; key hazard signal: IARC Group 3. Key regulatory status: REACH registered, 7 regulatory/inventory lists, cosmetic ingredient cross-reference; source data from EPA ToxValDB, EPA CPDat, AICIS, IARC, ECHA REACH, ILO ICSC.

View cosmetic safety profile for Diethylhexyl Adipate →

SOURCE noael studies public
NOAEL studies
62
SOURCE chemical inventory jurisdictions
Regulatory lists
7
SOURCE eu clp annex vi
GHS signal
Not classified

Chemical Identity

CAS, identifiers, formula, and alternate names for the matched substance record.

SOURCE DSSTox identifiers 26 fields
Name
Bis(2-ethylhexyl)hexanedioate
CAS Number
103-23-1
DTXSID
DTXSID0020606
Molecular Formula
C22H42O4
InChI Key
SAOKZLXYCUGLFA-UHFFFAOYSA-N
Monoisotopic Mass
370.30831
Synonyms
Adimoll DODEHAHexanedioic acid, bis(2-ethylhexyl) esterAdipic acid, bis(2-ethylhexyl) esterBRN 1803774Di(2-ethylhexyl)adipateEINECS 203-090-1Flexol plasticizer A-26Flexol plasticizer 10-AHexanedioic acid, dioctyl esterKemester 5652Mollan S

IARC Carcinogen Classification

Carcinogenic hazard classification from IARC monograph evaluations.

SOURCE IARC Monographs on the Identification of Carcinogenic Hazards to Humans 1 records
GroupMeaningEvaluatedVolume
Group 3Not classifiable2000Sup 7, 77

ICSC Chemical Safety

International Chemical Safety Card hazard and exposure summary.

SOURCE ILO/WHO International Chemical Safety Cards 1 records
FieldValue
GHS Signal WordWARNING
GHS Hazard StatementsCauses eye irritation May be harmful if swallowed and enters airways Very toxic to aquatic life
Short-term EffectsThe substance is mildly irritating to the eyes. If swallowed the substance easily enters the airways and could result in aspiration pneumonitis.

Functional Uses

Industrial and product-use categories associated with this substance.

SOURCE EPA CPDat 54 records
SolventSoftener and conditionerFilm formerPlasticizerDegradant/impurityNo specific technical functionPigmentFragranceLubricating agentDispersing agent

Regulatory Lists

Inventory, screening, and regulatory list matches from public chemical databases.

SOURCE EPA CPDat 7 records
ListKeywordSource
Europe; plastic_additiveEuropean Chemicals AgencyEuropean Chemicals Agency (ECHA)
Arts and crafts/Office supplies - home office - pens and markers; detected; EuropeDanish Environmental Protection AgencyDanish EPA
Indirect additives food contact (10/2018)FDAUnited States Food and Drug Administration (FDA)
IFRA TransparencyIFRAIFRA
consumer_productP&GProctor & Gamble
inert_ingredient; non_food_use; PesticidesEPACPCat
detected; Toys and children's productsJournal of Exposure Science & Environmental EpidemiologyPublished Articles

NOAEL Studies

Toxicology endpoints rendered from public NOAEL study rows.

SOURCE NOAEL studies Showing 50 of 62 studies
ValueUnitEndpointRouteSpeciesSource
13.56uL/min/10^6 cellsClint-HumanNTP_ICE_adme_parameters
MBY1SL921LUNIIFDA UNII substance identifier--openFDA substances
MBY1SL921LUNIIFDA UNII substance identifier--openFDA substances
MBY1SL921LUNIIFDA UNII substance identifier--openFDA substances
MBY1SL921LUNIIFDA UNII substance identifier--openFDA substances
0.03861fractionFu-HumanNTP_ICE_adme_parameters
3IARC groupIARC carcinogenicity classification--IARC Monographs
3IARC groupIARC carcinogenicity classification--IARC Monographs
3IARC groupIARC carcinogenicity classification--IARC Monographs
3unitlessIARC group--NTP_ICE_cancer
=5600mg/kg bwLD50oralRatNTP_ICE_acute_oral
=9100mg/kg bwLD50oralRatNTP_ICE_acute_oral
=9110mg/kg bwLD50oralRatNTP_ICE_acute_oral
=19100mg/kg bwLD50oralRatNTP_ICE_acute_oral
>20000mg/kg bwLD50oralRatNTP_ICE_acute_oral
=25000mg/kg bwLD50oralRat (Female)NTP_ICE_acute_oral
=45000mg/kg bwLD50oralRat (Male)NTP_ICE_acute_oral
=625mg/kg bw/dayLELoralRatToxValDB_ToxRefDB
=625mg/kg bw/dayLELoralrat (fischer; Fischer 344)ToxRefDB_ToxRefDB_v3_pod.csv
=945mg/kg bw/dayLELoralMouseToxValDB_ToxRefDB
=945mg/kg bw/dayLELoralmouse (b6c3f1; B6C3F1)ToxRefDB_ToxRefDB_v3_pod.csv
=1250mg/kg bw/dayLELoralRatToxValDB_ToxRefDB
=1250mg/kg bw/dayLELoralrat (fischer; Fischer 344)ToxRefDB_ToxRefDB_v3_pod.csv
=1800mg/kg bw/dayLELoralMouseToxValDB_ToxRefDB
=1800mg/kg bw/dayLELoralmouse (b6c3f1; B6C3F1)ToxRefDB_ToxRefDB_v3_pod.csv
=3750mg/kg bw/dayLELoralMouseToxValDB_ToxRefDB
=3750mg/kg bw/dayLELoralmouse (b6c3f1; B6C3F1)ToxRefDB_ToxRefDB_v3_pod.csv
=60625.9mg/m3LELinhalationHumanToxValDB_DOE_Protective_Action_Criteria
=1080mg/kg bw/dayLOAELoralRatToxValDB_IRIS
=2220mg/kg bw/dayLOAELoralMouseToxValDB_ECHA_IUCLID
=2500mg/kg bw/dayLOAELoralRatToxValDB_ToxRefDB
=2500mg/kg bw/dayLOAELoralrat (fischer; Fischer 344)ToxRefDB_ToxRefDB_v3_pod.csv
=7500mg/kg bw/dayLOAELoralMouseToxValDB_ToxRefDB
=7500mg/kg bw/dayLOAELoralmouse (b6c3f1; B6C3F1)ToxRefDB_ToxRefDB_v3_pod.csv
-unitlessModel Score--NTP_ICE_endocrine
>-mg/kg bw/dayNELoralmouse (b6c3f1; B6C3F1)ToxRefDB_ToxRefDB_v3_pod.csv
=240mg/kg bw/dayNELoralMouseToxValDB_ToxRefDB
=240mg/kg bw/dayNELoralmouse (b6c3f1; B6C3F1)ToxRefDB_ToxRefDB_v3_pod.csv
=315mg/kg bw/dayNELoralRatToxValDB_ToxRefDB
=315mg/kg bw/dayNELoralrat (fischer; Fischer 344)ToxRefDB_ToxRefDB_v3_pod.csv
=465mg/kg bw/dayNELoralMouseToxValDB_ToxRefDB
=465mg/kg bw/dayNELoralmouse (b6c3f1; B6C3F1)ToxRefDB_ToxRefDB_v3_pod.csv
=600mg/kg bw/dayNELoralRatToxValDB_ToxRefDB
=600mg/kg bw/dayNELoralrat (fischer; Fischer 344)ToxRefDB_ToxRefDB_v3_pod.csv
=625mg/kg bw/dayNELoralRatToxValDB_ToxRefDB
=625mg/kg bw/dayNELoralrat (fischer; Fischer 344)ToxRefDB_ToxRefDB_v3_pod.csv
=1875mg/kg bw/dayNELoralMouseToxValDB_ToxRefDB
=1875mg/kg bw/dayNELoralmouse (b6c3f1; B6C3F1)ToxRefDB_ToxRefDB_v3_pod.csv
~170mg/kg bw/dayNOAELoralRatToxValDB_ECHA_IUCLID
=170mg/kg bw/dayNOAELoralRatToxValDB_IRIS

Showing 50 of 62 studies

REACH Registration

Registration status from the ECHA REACH registered substances database.

SOURCE ECHA (EU) 1 records
StatusNameEC NumberLink
RegisteredBis(2-ethylhexyl) adipate203-090-1ECHA overview →

Australian Status (AICIS)

Australian industrial chemicals inventory status and applicable conditions.

SOURCE AICIS inventory 1 records
Inventory Status
listed

Cosmetic Safety Profile

Same-CAS cosmetic ingredient record for cross-vertical context.

SOURCE CosIng / Ingredients DB
EU Status
permitted
Max
-
Category
Emollient
View full cosmetic safety profile →

Pharmaceutical Data

Same-CAS pharmaceutical records from drug and bioactivity sources.

SOURCE EMBL-EBI ChEMBL CHEMBL1414950
ChEMBL Phase
Not listed
Adverse Events
0
Bioactivity
1
View full pharmaceutical profile →

Cannabis Data

Same-CAS cannabis compliance and lab records where available.

SOURCE Cannabis regulatory / lab data efsa substances

1 cannabis record found in efsa substances.

View full cannabis profile →

Frequently Asked Questions

What is the NOAEL for Bis(2-ethylhexyl)hexanedioate?

Bis(2-ethylhexyl)hexanedioate has 62 NOAEL studies in the database. The lowest reported value is 13.56 uL/min/10^6 cells in Human. Source: NTP_ICE_adme_parameters.

What regulatory lists include Bis(2-ethylhexyl)hexanedioate?

Bis(2-ethylhexyl)hexanedioate appears on 7 regulatory/inventory lists including Europe; plastic_additive, Arts and crafts/Office supplies - home office - pens and markers; detected; Europe, Indirect additives food contact (10/2018), and 4 more. Source: EPA CPDat.

Is Bis(2-ethylhexyl)hexanedioate a carcinogen according to IARC?

Bis(2-ethylhexyl)hexanedioate is classified by IARC as Group 3 — not classifiable as to its carcinogenicity to humans (evaluated 2000). Source: IARC Monographs on the Identification of Carcinogenic Hazards to Humans.

Is Bis(2-ethylhexyl)hexanedioate used in cosmetics?

Yes, Bis(2-ethylhexyl)hexanedioate is also indexed as a cosmetic ingredient under the name Diethylhexyl Adipate. 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 Bis(2-ethylhexyl)hexanedioate come from?

Safety data is sourced from EPA ToxValDB, EPA CPDat, AICIS (Australian Industrial Chemicals Introduction Scheme), EPA DSSTox, IARC Monographs, ECHA REACH, ILO/WHO ICSC, CosIng / Ingredients DB, ChEMBL / DailyMed, cannabis regulatory/lab databases. All data traces to primary regulatory sources and is updated from official government databases.

Does Bis(2-ethylhexyl)hexanedioate have different safety status in cosmetics vs industrial chemicals?

Bis(2-ethylhexyl)hexanedioate is classified GHS CMR hazard (H336, H361) in the chemicals database but is allowed in EU cosmetics.

Is Bis(2-ethylhexyl)hexanedioate used outside industrial chemicals?

Bis(2-ethylhexyl)hexanedioate also appears in cosmetics, pharmaceutical, cannabis databases.