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BUTYLENE GLYCOL
Chemical structure of BUTYLENE GLYCOL

BUTYLENE GLYCOL

CAS 107-88-0 (i), 6290-03-5 (ii) · humectant · EC 203-529-7 (i), 228-532-0 (ii) · KR 부틸렌글라이콜

Generally Low Concern5 citationsPregnancy safe

Butane-1,3-diol (CAS No. 107-88-0/ EC No. 203-529-7)
(R)-(-)-butane-1,3-diol” (CAS No. 6290-03-5/ EC No. 228-532-0)

BUTYLENE GLYCOL is a humectant ingredient used in skincare formulations.

hydrationsolventtexture enhancer
⚠️ Data is provided for informational purposes only. It may contain inaccuracies and should be independently verified. This is not medical advice. Consult a healthcare professional before making health decisions.

Quick facts

Description: BUTYLENE GLYCOL — hydration, solvent, texture enhancer.

All Functions: hydration, solvent, texture enhancer

Quick Facts:

  • Category: humectant

Proven Benefits At A Glance:

  • Butylene glycol is a humectant, meaning it helps skin retain moisture
  • When combined with other ingredients like glycerol, it may enhance hydration benefits
  • Research shows it can help maintain skin’s moisture barrier over an 8-hour period
  • Allergic reactions to butylene glycol are uncommon but possible for some people
  • It’s used in cosmetic extraction to pull beneficial compounds from plant sources

Chemical Overview

Butane-1,3-diol is a butanediol compound having two hydroxy groups in the 1- and 3-positions. It is a glycol and a butanediol. 1,3-Butanediol is found in pepper (c. annuum). 1,3-Butanediol is a solvent for flavouring agents 1,3-Butanediol is an organic chemical, an alcohol. It is commonly used as a solvent for food flavouring agents and is a co-monomer used in certain polyurethane and polyester resins. It is one of four stable isomers of butanediol. In biology, 1,3-butanediol is used as a hypoglycaemic agent. 1,3-Butanediol belongs to the family of Secondary Alcohols. These are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R’) (R,R’=alkyl, aryl). RN given refers to cpd without isomeric designation

Source(s): Medical Subject Headings (MeSH), ChEBI, Toxin and Toxin Target Database (T3DB), via PubChem

Comedogenicity

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