Poly(oxy-1,2-ethanediyl), -isodecyl–hydroxy- (CAS 61827-42-7) — Citrus N/A Note Fragrance Ingredient

Citrus · Floral

Poly(oxy-_1,_2-_ethanediyl)_, _-_isodecyl-__-_hydroxy-

CAS 61827-42-7

Origin
synthetic
Note
N/A
IFRA
Generally safe
Data as of: Apr 2026

What Is Poly(oxy-_1,_2-_ethanediyl)_, _-_isodecyl-__-_hydroxy-?

Poly(oxy-1,2-ethanediyl), α-isodecyl-ω-hydroxy- is a synthetic polymer used primarily as an emulsifier and stabilizer in cosmetic formulations. Consumers may encounter it in lotions, creams, and hair care products where it helps blend oil and water components. While not a fragrance ingredient itself, this compound plays a supporting role in scent delivery systems by improving the longevity and diffusion of fragrance oils in personal care products.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
Approved for cosmetic use
Avoid direct eye contact
CAS
61827-42-7
Formula
Mixture
MW
Variable
Odor Family
Citrus · Floral
Layer 1 · Enthusiast

What Does Poly(oxy-_1,_2-_ethanediyl)_, _-_isodecyl-__-_hydroxy- Smell Like?

This polymer is odorless and does not contribute directly to fragrance profiles. Its primary function is to modify the physical properties of fragrance formulations, enhancing texture and stability without altering scent characteristics.

Layer 2

2D Molecular Structure

Polyoxyethylene isodecyl ether

SMILES: CC(C)CCCCCCCOCCO

Chemistry, Properties & Perfumer Guide

The Chemistry

Poly(oxy-1,2-ethanediyl), α-isodecyl-ω-hydroxy- is a polyethylene glycol derivative with a hydrophobic isodecyl group and hydrophilic hydroxyl termination. This amphiphilic structure allows it to function as a nonionic surfactant. It’s synthesized through ethoxylation of isodecyl alcohol under controlled conditions. The polymer’s molecular weight distribution depends on the degree of ethoxylation during production.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
SolubilitySoluble in water and most organic solvents

Perfumer Guide

Note Position
N/A
Volatility
N/A
Blending
Functional additive
ApplicationTypical %RangeNotes
Emulsions1-5%0.5-10%Stabilizes fragrance oils
Hair Care2-8%1-15%Improves scent deposition

Classic Accords

Tip: Use as a co-emulsifier with primary surfactants for optimal fragrance oil incorporation.

Alternatives & Comparisons

1
PEG-40 Hydrogenated Castor Oil CAS 61788-85-0

Alternative emulsifier with similar HLB properties, often used when natural-derived ingredients are preferred.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

General reference only. Consult current IFRA Standards Library before formulating.

IFRA Status

Not restricted by IFRA as it is not a fragrance material.

RIFM Assessment

Not evaluated by RIFM as it is not a fragrance ingredient.

Sustainability

As a synthetic polymer, this material is petroleum-derived but requires relatively low energy inputs during manufacturing. Its high efficiency at low usage levels reduces overall environmental impact compared to some natural emulsifiers. Biodegradability depends on the degree of ethoxylation.

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References

  1. Cosmetic Ingredient Review Expert Panel (2012). Safety Assessment of Alkyl PEG Ethers as Used in Cosmetics. CIR Report
  2. EPA Chemical Data Access Tool record EPA Record

Data: PubChem (NIH), PubMed, RIFM, IFRA. Last reviewed: Apr 2026.

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Ingredient Data Sheet

CAS 61827-42-7

Physical Properties

Molecular Weight202.33 g/mol🔬 PubChem
LogP (Octanol-Water)3.7🔬 PubChem
log Kp (skin permeability)-1.307💻 Calculated
SMILESCC(C)CCCCCCCOCCO🔬 PubChem

Odor & Flavor

Functional Groupsalcoholether💻 RDKit
Data Sources & Attribution
Physical data: PubChem (NIH/NLM), U.S. EPA CompTox Dashboard, EPA OPERA models, RDKit. Odor & flavor: Arctander (Perfume & Flavor Chemicals), Fenaroli's Handbook of Flavor Ingredients, Leffingwell. Thresholds: van Gemert (Compilations of Odour Threshold Values). Regulatory: IFRA Standards 51st, FEMA GRAS. Trade names: Surburg (Common Fragrance & Flavor Materials). All data compiled and cross-referenced for perfumertools.com.

Physicochemical Properties

DTXSID: DTXSID7052810

Physical Properties

Molecular Weight 202.33 g/mol🔬 PubChem

Partition & Solubility

LogP (Octanol-Water) 3.7 Log10 unitless🔬 PubChem

Molecular Descriptors

Topological Polar Surface Area 29.46 Ų💻 Computed
H-Bond Donors 1 count💻 Computed
H-Bond Acceptors 2 count💻 Computed
Rotatable Bonds 10 count💻 Computed
Molar Refractivity 60.44 cm^3/mol💻 Computed

Data Sources:

🔬 EPA Experimental data from U.S. EPA CompTox Chemicals Dashboard & CTX APIs. 📊 OPERA Predicted using EPA's OPERA QSAR models. 💻 Computed Calculated from SMILES using RDKit.

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