| Size | Price | Stock | Qty |
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| 500mg |
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| 1g |
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| Other Sizes |
| Targets |
As an industrial solvent, butyl carbitol acetate does not have a specific pharmacological target. Its primary applications are as a solvent and penetrant in paints, coatings, cleaning products, and textiles. The compound may interact with biological systems through non-specific mechanisms.
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| ln Vitro |
Butyl carbitol acetate itself is not known to possess direct therapeutic activity. Its significance is as an industrial solvent and penetrant. The compound enables deep permeation into textiles due to its low vapor pressure and boiling point. It is used as a solvent in paints, coatings, and cleaning products.
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| ln Vivo |
There is no reported in vivo therapeutic activity for butyl carbitol acetate. The compound is primarily used as an industrial solvent in paints, coatings, cleaning products, and textiles. Its role in biological systems is as a solvent rather than a pharmacologically active compound.
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| Enzyme Assay |
As an industrial solvent, there are no standardized in vitro enzyme/receptor binding assays for butyl carbitol acetate. The compound's utility is in industrial applications such as paints, coatings, and cleaning products. Researchers may study the compound's physical and chemical properties, such as solubility, vapor pressure, and boiling point.
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| Cell Assay |
There are no reported in vitro cellular assays for butyl carbitol acetate as a therapeutic agent. The compound is used in industrial applications. Cellular studies may be conducted to assess the compound's toxicity or effects on cell viability, but these are not therapeutic assays.
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| Animal Protocol |
There are no reported in vivo animal studies for butyl carbitol acetate as a therapeutic agent. The compound is primarily used in industrial applications. Animal studies may be conducted to assess the compound's toxicity, but these are not therapeutic studies.
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| ADME/Pharmacokinetics |
Absorption, Distribution and Excretion
When diethylene glycol butyl ether (DGBE) and diethylene glycol monobutyl ether acetate (DGBEA) were applied to the skin and then washed off after 5 minutes, most (90%) of the substance was recovered. After 24 hours of administration under closed conditions, the calculated absorption rate of DGBEA (male 1.58 mg/cm²/hr, female 1.28 mg/cm²/hr; mean = 1.43) was similar to that of DGBE (male 0.73 mg/cm²/hr, female 1.46 mg/cm²/hr; mean = 1.10 mg/cm²/hr). DGBEA is rapidly absorbed from the gastrointestinal tract and is primarily (85% of the dose) excreted in the urine after metabolism. Following oral administration of 200 or 2000 mg/kg of 14C-DGBA, it is rapidly absorbed from the gastrointestinal tract and primarily excreted in the urine of rats within 24 hours. The main urinary metabolite was 2-(2-butoxyethoxy)acetic acid. No unmetabolized DGBA or DGBE was detected in rat urine at either dose level. Metabolites/Metabolites: Following transdermal administration of diethylene glycol monobutyl ether acetate, the main urinary metabolite detected was 2-(2-butoxyethoxy)acetic acid (50-60%), along with a small amount of glucuronide conjugates of DGBE (5-8%). This study investigated the in vitro hydrolysis of diethylene glycol monobutyl ether acetate (DGBA) in rat blood and its metabolism and distribution in male Sprague-Dawley rats. DGBA (5 mM) is hydrolyzed in rat blood to diethylene glycol monobutyl ether (DGBE) with a half-life of less than 3 minutes. 14C-DGBA is rapidly absorbed from the gastrointestinal tract and is primarily excreted in rat urine within 24 hours after oral administration of 200 or 2000 mg/kg. The primary urinary metabolite is 2-(2-butoxyethoxy)acetic acid. Unmetabolized DGBA or DGBE was not detected in rat urine at either dose level. Biological half-life DGBA (5 mM) is hydrolyzed in rat blood to diethylene glycol monobutyl ether (DGBE), with a half-life of less than 3 minutes. Butyl carbitol acetate has a molecular weight of 204.26 and a molecular formula of C10H20O4. It is a colorless liquid with a faint, fruity smell, a melting point of -32°C, a boiling point of 245°C, and a density of 0.977 g/mL at 20°C. The compound has low vapor pressure. |
| Toxicity/Toxicokinetics |
Toxicity Data
LC50 (Rat) = 72,500 mg/m³/4h Butyl carbitol acetate is considered safe for its intended industrial uses. The compound should be handled with appropriate safety precautions, including the use of personal protective equipment. Toxicological studies support its use in industrial applications. |
| Additional Infomation |
Diethylene glycol monobutyl ether acetate is a colorless liquid with a slight odor. It floats on water and dissolves slowly. (US Coast Guard, 1999)
Butyl carbitol acetate (2-(2-butoxyethoxy)ethyl acetate, diethylene glycol monobutyl ether acetate) is a high-performance glycol ether ester used as a solvent in paints, coatings, cleaning products, and textiles. It is a colorless liquid with a faint, fruity smell, a boiling point of 245°C, and a density of 0.977 g/mL. The compound enables deep permeation into textiles due to its low vapor pressure. |
| Molecular Formula |
C10H20O4
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|---|---|
| Molecular Weight |
204.27
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| Exact Mass |
204.136
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| CAS # |
124-17-4
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| PubChem CID |
31288
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| Appearance |
Colorless liquid
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| Density |
0.977 g/mL at 20 °C(lit.)
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| Boiling Point |
245 °C(lit.)
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| Melting Point |
-32 °C
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| Flash Point |
105 °C
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| Vapour Pressure |
8.03E-06mmHg at 25°C
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| Index of Refraction |
n20/D 1.426
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| LogP |
1.382
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| Hydrogen Bond Donor Count |
0
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| Hydrogen Bond Acceptor Count |
4
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| Rotatable Bond Count |
10
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| Heavy Atom Count |
14
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| Complexity |
136
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| Defined Atom Stereocenter Count |
0
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| SMILES |
CCCCOCCOCCOC(=O)C
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| InChi Key |
VXQBJTKSVGFQOL-UHFFFAOYSA-N
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| InChi Code |
InChI=1S/C10H20O4/c1-3-4-5-12-6-7-13-8-9-14-10(2)11/h3-9H2,1-2H3
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| Chemical Name |
2-(2-butoxyethoxy)ethyl acetate
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| Synonyms |
NSC-5175; NSC 5175; Butyl carbitol acetate
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| HS Tariff Code |
2934.99.9001
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| Storage |
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
| Shipping Condition |
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
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| Solubility (In Vitro) |
May dissolve in DMSO (in most cases), if not, try other solvents such as H2O, Ethanol, or DMF with a minute amount of products to avoid loss of samples
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| Solubility (In Vivo) |
Note: Listed below are some common formulations that may be used to formulate products with low water solubility (e.g. < 1 mg/mL), you may test these formulations using a minute amount of products to avoid loss of samples.
Injection Formulations
Injection Formulation 1: DMSO : Tween 80: Saline = 10 : 5 : 85 (i.e. 100 μL DMSO stock solution → 50 μL Tween 80 → 850 μL Saline)(e.g. IP/IV/IM/SC) *Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH ₂ O to obtain a clear solution. Injection Formulation 2: DMSO : PEG300 :Tween 80 : Saline = 10 : 40 : 5 : 45 (i.e. 100 μL DMSO → 400 μLPEG300 → 50 μL Tween 80 → 450 μL Saline) Injection Formulation 3: DMSO : Corn oil = 10 : 90 (i.e. 100 μL DMSO → 900 μL Corn oil) Example: Take the Injection Formulation 3 (DMSO : Corn oil = 10 : 90) as an example, if 1 mL of 2.5 mg/mL working solution is to be prepared, you can take 100 μL 25 mg/mL DMSO stock solution and add to 900 μL corn oil, mix well to obtain a clear or suspension solution (2.5 mg/mL, ready for use in animals). View More
Injection Formulation 4: DMSO : 20% SBE-β-CD in saline = 10 : 90 [i.e. 100 μL DMSO → 900 μL (20% SBE-β-CD in saline)] Oral Formulations
Oral Formulation 1: Suspend in 0.5% CMC Na (carboxymethylcellulose sodium) Oral Formulation 2: Suspend in 0.5% Carboxymethyl cellulose Example: Take the Oral Formulation 1 (Suspend in 0.5% CMC Na) as an example, if 100 mL of 2.5 mg/mL working solution is to be prepared, you can first prepare 0.5% CMC Na solution by measuring 0.5 g CMC Na and dissolve it in 100 mL ddH2O to obtain a clear solution; then add 250 mg of the product to 100 mL 0.5% CMC Na solution, to make the suspension solution (2.5 mg/mL, ready for use in animals). View More
Oral Formulation 3: Dissolved in PEG400  (Please use freshly prepared in vivo formulations for optimal results.) |
| Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
| 1 mM | 4.8955 mL | 24.4774 mL | 48.9548 mL | |
| 5 mM | 0.9791 mL | 4.8955 mL | 9.7910 mL | |
| 10 mM | 0.4895 mL | 2.4477 mL | 4.8955 mL |
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.
Calculation results
Working concentration: mg/mL;
Method for preparing DMSO stock solution: mg drug pre-dissolved in μL DMSO (stock solution concentration mg/mL). Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation::Take μL DMSO stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O,mix and clarify.
(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
(2) Be sure to add the solvent(s) in order.