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4-Butylresorcinol

CAS No.
18979-61-8
Chemical Name:
4-Butylresorcinol
Synonyms
4-N-BUTYLRESORCINOL;Butylresorcinol;4-Butylbenzene-1,3-diol;Rucinol;4-phenylbutane-1,3-diol;2,4-DIHYDROXY-N-BUTYL BENZEN;N-BUTYLRESEOCINOL;4-Butylresorcinol;Serine Impurity 12;4-Butylresorcinol1
CBNumber:
CB9361328
Molecular Formula:
C10H14O2
Molecular Weight:
166.22
MDL Number:
MFCD01684800
MOL File:
18979-61-8.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-27 17:00:41

4-Butylresorcinol Properties

Melting point 50.0 to 55.0 °C
Boiling point 166°C/7mmHg(lit.)
Density 1.092±0.06 g/cm3(Predicted)
vapor pressure 0.041Pa at 25℃
storage temp. Inert atmosphere,Room Temperature
solubility DMSO : 150 mg/mL (902.42 mM)
form Powder
pka 9.95±0.18(Predicted)
color white to pale yellow powder
Odor Characteristic
Major Application cleaning products
cosmetics
food and beverages
personal care
Cosmetics Ingredients Functions ANTIOXIDANT
InChI InChI=1S/C10H14O2/c1-2-3-4-8-5-6-9(11)7-10(8)12/h5-7,11-12H,2-4H2,1H3
InChIKey CSHZYWUPJWVTMQ-UHFFFAOYSA-N
SMILES C1(O)=CC=C(CCCC)C(O)=C1
LogP 2.8 at 24℃ and pH7
Surface tension 17.8mN/m at 1g/L and 20℃
CAS DataBase Reference 18979-61-8(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 2IK4UQ3ZGA
UNSPSC Code 85151701
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319
Precautionary statements  P264-P270-P280-P301+P312+P330-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P501
WGK Germany  WGK 2
RTECS  VH0420000
HS Code  2907290090
Storage Class 13 - Non Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
Aquatic Acute 1
Eye Irrit. 2
Skin Irrit. 2
REACH Registrations Inactive
NFPA 704
0
2 0

4-Butylresorcinol price More Price(71)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 49797 4-Butylresorcinol analytical standard 18979-61-8 100 mg $229 2026-04-30 Buy
TCI Chemical B3773 4-Butylresorcinol >98.0%(GC) 18979-61-8 1g $257 2026-04-30 Buy
Biosynth FB168030 4-n-Butylresorcinol 18979-61-8 0.005kg $276.01 2026-06-04 Buy
Biosynth FB168030 4-n-Butylresorcinol 18979-61-8 0.01kg $456.21 2026-06-04 Buy
Biosynth FB168030 4-n-Butylresorcinol 18979-61-8 0.025kg $852.49 2026-06-04 Buy
Product number Packaging Price Buy
49797 100 mg $229 Buy
B3773 1g $257 Buy
FB168030 0.005kg $276.01 Buy
FB168030 0.01kg $456.21 Buy
FB168030 0.025kg $852.49 Buy

4-Butylresorcinol Chemical Properties, Uses, Production

resorcinol derivative

4-n-Butylresorcinol is a resorcinol derivative that inhibits both tyrosinase and tyrosinase-related protein-1 (TRP-1). It may be used to decrease skin irritation and is also known to inhibit melanin production. Its hypopigmenting action was first reported in 1995, and many following studies have documented its efficacy and safety in melasma treatment with the 0.1% cream, but there is paucity of clinical studies that used the 0.3% cream. The biochemical assay on inhibition of human tyrosinase activity has revealed the superiority of 4-n-butylresorcinol over other hypopigmenting agents. Many studies show good efficacy and safety in treating melisma.
4-n-Butylresorcinol
4-n-Butylresorcinol may be used to produce a safe cosmetic agent, with the clinical efficacy required of a pharmacological agent. Furthermore, 4-n-butylresorcinol acts mainly by inhibition of tyrosinase activity and has no effect on MITF. 4-n-butylresorcinol showed an additive effect in combination with hinokitiol, which reduces MITF expression.

History

4-n-Butylresorcinol (Rucinol® ) (Obtained by POLA in 1998) was selected by screening synthetic resorcinol derivatives that can elicit strong competitive inhibition of tyrosinase activity. Melanin synthesis is catalyzed by tyrosinase, together with tyrosinase-related proteins (TRP) -1 and -2, and Rucinol® has been shown to inhibit melanin synthesis in cultured mouse melanocytes via direct inhibition not only of tyrosinase activity, but also of TRP-1 activity. A 0.3% Rucinol® -containing lotion was shown to be effective for treating hyperpigmentary disorders, such as melasma.

Uses

4-Butylresorcinol(18979-61-8) is considered a potential Cytochrome P450 inhibitor. It can cause hypopigmentation due to its direct inhibition of tyrosinase.

tyrosinase inhibitor

4-butylresorcinol(18979-61-8) is use as an effective treatment option for topical hyperpigmentation management. Similar to hydroquinone, 4-n-butylresorcinol is also a tyrosinase inhibitor. It has been characterized as a strong tyrosinase25 and TRP‐126 inhibitor. We measured an IC50 in the human tyrosinase assay of 21μmol/L for 4‐butylresorcinol compared with 94 and 131?μmol/L for 4‐hexylresorcinol and 4‐phenylethylresorcinol respectively. Also on skin models, 4‐butylresorcinol was most effective of all tested substances with an IC50 of 13.5 μmol/L. Therefore, 4‐butylresorcinol was selected for several clinical studies to prove in vivo efficacy. In comparison with 4‐hexylresorcinol and 4‐phenylethylresorcinol, 4‐butylresorcinol treated age spots showed a faster onset of improvement and also a higher degree of lightening after 12 weeks of treatment.

Description

4-n-butylresorcinol is a derivative of resorcinol and a potent human tyrosinase inhibitor. It may be used to decrease skin irritation and is also known to inhibit melanin production.

Uses

4-Butylresorcinol is considered a potential Cytochrome P450 inhibitor. It can cause hypopigmentation due to its direct inhibition of tyrosinase.

Definition

ChEBI: 4-n-Butylresorcinol is a member of resorcinols.

Application

Glycerol is used both in sample preparation and gel formation for polyacrylamide gel electrophoresis. Glycerol (5-10%) increases the density of a sample so that the sample will layer at the bottom of a gel′s sample well. Glycerol is also used to aid in casting gradient gels and as a protein stabilizer and storage buffer component.

Biological Activity

Glutathione reductase IGR) is a crucial flavoenzyme in the antioxidant defense system. Reduced glutathione (GSH) is used by glutathione peroxidase to detoxify hydrogen peroxide and in the process is converted to oxidized glutathione (GSSG). The GSSG is then recycled back to GSH by glutathione reductase (GR) using NADPH that is then converted to NADP+. The regenerated GSH is then available to detoxify more hydrogen peroxide. The enzyme uses FAD as a cofactor. GR and glutathione peroxidase may inhibit lipid peroxidation by functioning as antioxidant enzymes in sperm. Glutathione reductase shares a structural motif with a number of other proteins including aspartyl proteases, citrate synthase, EF hands, hemoglobins, lipocalins, and α/β hydrolases. GR is stimulated by melatonin and is reportedly irreversibly inhibited by a number of oxygen radical generating systems.A sweet tastant for mammals. A glycerol taste receptor binding site specific for glucose has been proposed in drosophila.

Mechanism of action

The mechanism of action of 4-butylresorcinol depigmentation is through inhibition of tyrosinase and tyrosinase-related protein-1 (TRP-1)[1].

Synthesis

Synthesis_18979-61-8
Under the protection of nitrogen, 110 g (1 mol) of resorcinol and 220 g of n-heptane were mixed in the reaction flask, heated and dissolved, and the temperature was lowered to 10 C. A turbid solution of 40.8 g (1.02 mol) of sodium hydroxide and 100 g of n-butanol was added in portions. , And control the temperature of 10 to 15 , after TLC (EA developing agent) detection of almost no remaining raw materials, add n-butanol (2.5mol), tris (pentafluorobenzene) borane 17.5g (0.1mol) and calcium chloride 1.1 g, raise the temperature to 40-45 C for 1 hour, then raise the temperature to 98 C for reflux and water separation. After 8 hours of water separation, take a sample and quench the GC to detect resorcinol <1%, cool to room temperature, add a small amount of water to quench It is extinguished, and then dilute sulfuric acid is added to adjust the pH = 1-2. The insoluble solids are filtered through diatomaceous earth, and the organic phase is concentrated to a stagnant liquid. Water is added for replacement, and then 660 g of water, 2.2 g of sodium thiosulfate, and 5.5 g are added. Activated carbon was heated to reflux for 1 hour, and was hot-filtered to obtain a pale yellow solution. Then, flaky crystals were precipitated by cooling, and 151 g of 4-n-butylresorcinol was obtained by filtration, GC: 99.3%, and yield: 90.9%.

References

[1] D. RESENDE. Skin Depigmenting Agents in Anti-Aging Cosmetics: A Medicinal Perspective on Emerging Ingredients[J]. Applied Sciences-Basel, 2022. DOI:10.3390/app12020775.

4-Butylresorcinol Preparation Products And Raw materials

Global Suppliers ( 586)
Supplier Tel Email Country ProdList Advantage
Hubei ZhongKe XinChen Technology Ltd. 欢迎详询+微信 18827688560 starvips@qq.com China 496 58
Taizhou Ruishinuo Pharmaceutical Technology Co., Ltd. 0523-86848872 19952992164;18652727964; 725236090@qq.com China 98 58
Hubei YiKangYuan Chemical Co., Ltd. 027-87182908 18064088908 65824125@qq.com China 90 55
Hangzhou Linran Biotechnology Co. LTD 0571-18067987-92 18067987892;13738142397 2543558860@qq.com China 137 58
Beri Pharma Co., Ltd. 13427714006 sales@zhberi.com China 19 58
Shanghai Xuentian Technology Co.,Ltd. +86-186 6172 2072; 18661722072 mk@xuentian.cn China 250 58
Nanjing XiLang Chemical Products Co., Ltd. 18936048580 chemxilang@163.com China 3909 58
Meite (Hubei) New Materials Co., Ltd 13517221830; 13517221830 18802755@qq.com China 2612 58
Zhuhai Huachen Pharmaceutical Technology Co., Ltd 15916275916 290113728@qq.com China 52 58
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76

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View Latest Price from 4-Butylresorcinol manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
4-Butylresorcinol pictures 2026-09-19 4-Butylresorcinol
18979-61-8
0.99 RongNa Biotechnology Co.,Ltd
4-Butylresorcinol pictures 2026-09-02 4-Butylresorcinol
18979-61-8
$1.00-50.00 1KG 99% Henan Fengda Chemical Co., Ltd
4-Butylresorcinol pictures 2026-08-09 4-Butylresorcinol
18979-61-8
99% 2000kgs Chongqing Zhihe Biopharmaceutical Co., Ltd.

4-Butylresorcinol Spectrum

4-BUTYLRESORCINOL,98+% 4-Butylresorcinol 1,3-Benzenediol,4-butyl- 2,4-DIHYDROXY-N-BUTYL BENZENE 2,4-DIHYDROXY-N-BUTYL BENZEN 2,4-Dihydroxy-n-bytyl benzen 4-06-00-06003 (Beilstein Handbook Reference) N-BUTYLRESEOCINOL Nano Liposomal N-BUTYLRESEOCINOL 2,4-Dihydroxy-n-bytyl benzene 4-BUTYLBENZENE-1 3-DIOL(COSMOBRITE) 4-n-Butylresorcinol, Rucinol Nano-Liposomal 4-Butylresorcinol 4-Butylresorcinol > KOPCINOL – N-Butyl Resorcinol TIANFU-CHEM 18979-61-8 4-Butylresorcinol (Butylresorcinol) low price 18979-61-8 On Sale4-N-Butylresorcinol exporter 4-Butyl Resorcinol (4-BR) Resorcinol, 4-butyl- 4-Butylresorcinol CAS 4-Butylresorcinol/ 4-N-Butylresorcinol 4-Butylresorcinol a highly effective tyrosinase inhibitorn Serine Impurity 12 4-Butylresorcinol, 10 mM in DMSO 4-Butylpyrocatechol、4-Butyl-1,2-benzenediol 4-Butylresorcinol1 4-Butylresorcinol (Standard) 4-Butylbenzene-1,3-diol 4-phenylbutane-1,3-diol 4-N-BUTYLRESORCINOL Butylresorcinol Rucinol 18979-61-8 18879-61-8 Benzene derivates Miscellaneous pharmaceutical 18979-61-8