4 syllables: Hy, dro, quin, one. Stress on quin.
heye-droh-KWEYE-nohn
/ˌhaɪdroʊˈkwaɪnoʊn/
Hydroquinone is pronounced heye-droh-KWEYE-nohn (/ˌhaɪdroʊˈkwaɪnoʊn/). It has four syllables (Hy-dro-quin-one), with the stress on "quin". Hydroquinone is a chemical compound used primarily as a skin-lightening agent and as an intermediate in chemical synthesis. It consists of a benzene ring with two hydroxyl groups and a para-substituted ketone, forming a stable, white to off-white solid. In practice, it is handled as a controlled substance in many contexts due to safety concerns and regulatory status.
nounHydroquinone is a chemical compound used primarily as a skin-lightening agent and as an intermediate in chemical synthesis. It consists of a benzene ring with two hydroxyl groups and a para-substituted ketone, forming a stable, white to off-white solid. In practice, it is handled as a controlled substance in many contexts due to safety concerns and regulatory status.
"The dermatologist prescribed hydroquinone cream to treat hyperpigmentation."
"Industrial chemists synthesize hydroquinone via oxidation of hydroquinone precursors under controlled conditions."
"Certain hair-removal products include hydroquinone as an active ingredient for oxidative hair treatment."
Hydroquinone is pronounced hi-dro-KWĪ-nōn, with the primary stress on the third syllable (KWĪ). Phonetically: US /ˌhaɪdroʊˈkwɪnoʊn/, UK /ˌhaɪdrəˈkwɪnəʊn/, AU /ˌhaɪdroʊˈkwɪnoʊn/. Start with hi as in high, follow with dro, then KWI as in quick without the k sound fully de-voiced, and end with nōn as in tone. You’ll feel the tongue rise toward the palate for the /kw/ cluster, and the final /oʊn/ lands with a rounded, tense vowel plus nasal /n/.
Common errors include misplacing the stress (often stressing the first syllable instead of the third), mispronouncing the /kw/ cluster as separate /k/ and /w/ with an audible pause, and assuming the final -one is pronounced as a short /ʌn/ instead of /oʊn/. Correct by practicing the three-syllable rhythm, keeping /kw/ as a single consonant blend, and lengthening the final /oʊn/ to mirror tone. Use minimal pairs to train the final vowel.
In US and AU accents, the word is typically /ˌhaɪdroʊˈkwɪnoʊn/, with a clear /oʊ/ in the first syllable and final /oʊn/. UK pronunciation often features a slightly reduced middle vowel and a non-rhotic /r/ influence, yielding /ˌhaɪdrəˈkwɪnəʊn/. The main differences lie in rhoticity and vowel quality: Americans pronounce the final syllable with a strong /oʊn/, while UK speakers may have a shorter /ə/ in the middle syllable and a longer, rounded /əʊ/ in the final. Practicing with regional audio will help align your own pronunciation with your audience.
It combines a multisyllabic rhythm, a challenging /kw/ cluster, and a final long /oʊn/ that can blur into /oʊn/ for non-native speakers. The middle syllable /ˈkwɪn/ has a quick, tight vowel sequence, and the trailing /oʊn/ can be shortened in fast speech. Focus on the /kw/ blend and keep the final nucleus stable with a rounded, tense /oʊ/ before nasal /n/. Slow, deliberate practice with IPA cues helps stabilize these movements.
A distinctive aspect is maintaining the strong, compact /kw/ onset of the stressed syllable, avoiding a split or separate /k/ and /w/. The correct flow is hi-dro-KWĪ-nōn, with the emphasis fully on the third syllable. Many learners misplace the stress on the second syllable or soften the /kw/ into /k/ + /w/. Emphasize the /KW/ blend and keep the final long vowel rounded.
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Hydroquinone derives from hydro- indicating a hydrogen-backed structure and quinone-related chemistry. The term quinone itself comes from the German Quinol, influenced by the chemical family quinones first identified in the 19th century. Hydro- signals the presence of hydrogen or water-related derivation, while -quinone indicates a benzene ring with two carbonyl or quinone-type oxidation states in the core structure. The compound is formally named 1,4-dihydroxybenzene-1-one in some contexts, reflecting its para-dihydroxy substitution with a carbonyl. First isolated in the early 20th century through oxidation processes of phenolic compounds, hydroquinone quickly found use in industrial chemistry and, later, in dermatology for skin-lightening products, though regulatory restrictions emerged due to safety concerns. Its historical development tracks with the broader discovery of phenolic reducing agents and the expansion of aromatic chemistry, where para-substituted dihydroxy derivatives were synthesized to achieve specific redox properties. In pharmacology and cosmetics, hydroquinone’s ability to inhibit melanin synthesis has driven both therapeutic use and regulatory scrutiny, culminating in standardized usage guidelines and restricted concentrations worldwide. Linguistically, the name reflects a fusion of hydro- (water/derivative) and quinone (aromatic diketone), mirroring its chemical lineage and the nomenclature conventions of organic chemistry that emphasize functional groups and substitution patterns. First known use in chemistry literature appears in the early 1900s, with explicit references to hydroquinone's properties and applications following incremental synthetic methods developed in the mid-20th century.
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Words that rhyme with "Hydroquinone"
-ine sounds
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