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エチレングリコールモノブチルエーテル 化学構造式
2-be;BuCs;egbe;butycel;a13-0993;chimecnr;gafcoleb;Chimec NR;dowanoleb;Gafcol EB
MOL File:

エチレングリコールモノブチルエーテル 物理性質

融点 :
-70 °C
沸点 :
171 °C
比重(密度) :
0.902 g/mL at 25 °C(lit.)
4.1 (vs air)
<1 mm Hg ( 20 °C)
屈折率 :
n20/D 1.419(lit.)
闪点 :
140 °F
貯蔵温度 :
Store below +30°C.
900g/l completely miscible
外見 :
臭い (Odor):
Mild, characteristic; slightly rancid; mild ethereal.
7 (H2O, 20℃)(as aqueous solution)
爆発限界(explosive limit):
臭気閾値(Odor Threshold):
水溶解度 :
極大吸収波長 (λmax):
λ: 230 nm Amax: 1.0
λ: 250 nm Amax: 0.10
λ: 275 nm Amax: 0.05
λ: 300-400 nm Amax: 0.01
Merck :
Henry's Law Constant:
(x 10-6 atm?m3/mol): 2.36 (approximate - calculated from water solubility and vapor pressure)
TLV-TWA skin 25 ppm (121 mg/m3) (ACGIH), 50 ppm (242 mg/m3) (OSHA); STEL 75 ppm (363 mg/m3) (ACGIH);IDLH 700 ppm (NIOSH). .
CAS データベース:
111-76-2(CAS DataBase Reference)
3 (Vol. 88) 2006
Ethylene glycol monobutyl ether (111-76-2)
  • リスクと安全性に関する声明
  • 危険有害性情報のコード(GHS)
主な危険性  Xn
Rフレーズ  20/21/22-36/38
Sフレーズ  36/37-46
RIDADR  1986
WGK Germany  1
RTECS 番号 KJ8575000
自然発火温度 473 °F
HSコード  2909 43 00
国連危険物分類  6.1
容器等級  III
有毒物質データの 111-76-2(Hazardous Substances Data)
毒性 LD50 orally in rats: 1.48 g/kg (Smyth)
消防法 危険物第4類第二石油類(水溶性)
化審法 (2)-407, (2)-2424, (7)-97 優先評価化学物質
安衛法 有機則 第二種有機溶剤等
注意喚起語 Warning
コード 危険有害性情報 危険有害性クラス 区分 注意喚起語 シンボル P コード
H227 引火性液体 引火性液体 4 警告 P210, P280, P370+P378, P403+P235,P501
H302 飲み込むと有害 急性毒性、経口 4 警告 P264, P270, P301+P312, P330, P501
H312 皮膚に接触すると有害 急性毒性、経皮 4 警告 P280,P302+P352, P312, P322, P363,P501
H315 皮膚刺激 皮膚腐食性/刺激性 2 警告 P264, P280, P302+P352, P321,P332+P313, P362
H319 強い眼刺激 眼に対する重篤な損傷性/眼刺激 性 2A 警告 P264, P280, P305+P351+P338,P337+P313P
H330 吸入すると生命に危険 急性毒性、吸入 1, 2 危険 P260, P271, P284, P304+P340, P310,P320, P403+P233, P405, P501
H332 吸入すると有害 急性毒性、吸入 4 警告 P261, P271, P304+P340, P312
H335 呼吸器への刺激のおそれ 特定標的臓器毒性、単回暴露; 気道刺激性 3 警告
H361 生殖能または胎児への悪影響のおそれの疑い 生殖毒性 2 警告 P201, P202, P281, P308+P313, P405,P501
H370 臓器の障害 特定標的臓器有害性、単回暴露 1 危険 P260, P264, P270, P307+P311, P321,P405, P501
H373 長期にわたる、または反復暴露により臓器の障 害のおそれ 特定標的臓器有害性、単回暴露 2 警告 P260, P314, P501
P201 使用前に取扱説明書を入手すること。
P202 全ての安全注意を読み理解するまで取り扱わないこ と。
P210 熱/火花/裸火/高温のもののような着火源から遠ざ けること。-禁煙。
P260 粉じん/煙/ガス/ミスト/蒸気/スプレーを吸入しないこ と。
P264 取扱い後は皮膚をよく洗うこと。
P264 取扱い後は手や顔をよく洗うこと。
P270 この製品を使用する時に、飲食または喫煙をしないこ と。
P271 屋外または換気の良い場所でのみ使用すること。
P280 保護手袋/保護衣/保護眼鏡/保護面を着用するこ と。
P284 呼吸用保護具を着用すること。

エチレングリコールモノブチルエーテル 価格 もっと(36)

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入
富士フイルム和光純薬株式会社(wako) W01W0105-0263 2-ブトキシエタノール 98.0+% (Capillary GC)
2-Butoxyethanol 98.0+% (Capillary GC)
111-76-2 500mL ¥1500 2021-03-23 購入
富士フイルム和光純薬株式会社(wako) W01W0105-0371 2-ブトキシエタノール 99.0+% (Capillary GC)
2-Butoxyethanol 99.0+% (Capillary GC)
111-76-2 500mL ¥1680 2021-03-23 購入
東京化成工業 B0698 エチレングリコールモノブチルエーテル >99.0%(GC)
Ethylene Glycol Monobutyl Ether >99.0%(GC)
111-76-2 25mL ¥1600 2021-03-23 購入
東京化成工業 B0698 エチレングリコールモノブチルエーテル >99.0%(GC)
Ethylene Glycol Monobutyl Ether >99.0%(GC)
111-76-2 500mL ¥2600 2021-03-23 購入
関東化学株式会社(KANTO) 14123-00 2‐n‐ブトキシエタノール >98.0%(GC)
2‐n‐Butoxyethanol >98.0%(GC)
111-76-2 500mL ¥1700 2021-03-23 購入

エチレングリコールモノブチルエーテル 化学特性,用途語,生産方法














2-Butoxyethanol is a clear, colourless liquid with ether-like smell.2-Butoxyethanol is usually produced by a reaction of ethylene oxide with butyl alcohol, but it may also be made by the reaction of ethylene glycol with dibutyl sulphate. 2-Butoxyethanol is widely used as a solvent in protective surface coatings such as spray lacquers, quick-dry lacquers, enamels, varnishes, and latex paints. It is also used as an ingredient in paint thinners and strippers, varnish removers, agricultural chemicals, herbicides, silicon caulks, cutting oils, and hydraulic fluids and as metal cleaners, fabric dyes and inks, industrial and household cleaners (as a degreaser), and dry-cleaning compounds. It is also used in liquid soaps and in cosmetics. 2-Butoxyethanol acetate has been reported to be present in air, water, and soil as a contaminant and exposure to it occurs during its manufacture and use as an intermediate in the chemical industry, and during the formulation and use of its products in multiple industrial activities. The acetate form of 2-butoxyethanol is 2-butoxyethanol acetate and also known as ethylene glycol monobutyl ether acetate.


Ethylene glycol monobutyl ether is a colorless liquid with a mild, rancid, ether-like odor. It is miscible in alI proportions with many ketones, ethers, alcohols, aromatic paraffin and halogenated hydrocarbons. More specifically, it mixes in all proportions with acetone, benzene, carbon tetrachloride, ethyl ether, n-heptane and water. Because of its excellent solvency, low evaporation rate and high dilution ratios, it is used as a solvent in the manufacture and formulation of lacquers, enamels, inks and varnishes, employing such resins as alkyd, phenolic, nitrocellulose, maleic modified, styrene and epoxy. In lacquers butyl "Cellosolve" imparts a slow evaporation rate, strengthens blush resistance, heightens gloss, improves flow-out and helps prevent orange peel. Hot spray lacquers usually contain about 10% of "Dowanol" EB based on the solvent-diluent weight.


2-Butoxyethanol is a clear colorless liquid with an ether-like smell and belongs to the family of glycol ether/alkoxy alcohol. 2-Butoxyethanol is miscible in water and soluble in most organic solvents. 2-Butoxyethanol does not occur naturally. It is usually produced by reacting ethylene oxide with butyl alcohol.
2-Butoxyethanol is used as a solvent for nitrocellulose, natural and synthetic resins, soluble oils, in surface coatings, spray lacquers, enamels, varnishes, and latex paints, as an ingredient in paint thinners, quick-dry lacquers, latex paint, and strippers, varnish removers, and herbicides. It is also used in textile dyeing and printing, in the treatment of leather, in the production of plasticizers, as a stabilizer in metal cleaners and household cleaners, and in hydraulic fl uids, insecticides, herbicides, and rust removers. It is also used as an ingredient in liquid soaps, cosmetics, industrial and household cleaners, dry-cleaning compounds, and as an ingredient in silicon caulks, cutting oils, and hydraulic fluids. 2-Butoxyethanol is a fire hazard when exposed to heat, sparks, or open flames.


Clear, colorless, oily liquid with a mild, ether-like odor. Experimentally determined detection and recognition odor threshold concentrations were 500 μg/m3 (100 ppbv) and 1.7 mg/m3 (350 ppbv), respectively (Hellman and Small, 1974). An odor threshold concentration of 580 ppbv was reported by Nagata and Takeuchi (1990).


Ethylene glycol n-butyl ether (EB) is used widely as a coupling solvent because of its superior coupling efficiency and excellent solvency for resins.


Ethylene glycol monobutyl ether (EGBE) is used as a solvent for nitrocellulose, resins, oil, and grease, and in dry cleaning.


Solvent for nitrocellulose, resins, grease, oil, albumin; dry cleaning.

Synthesis Reference(s)

The Journal of Organic Chemistry, 45, p. 1095, 1980 DOI: 10.1021/jo01294a034


A colorless liquid with a mild, pleasant odor. Less dense than water. Flash point 160°F. Irritates skin and eyes and may be toxic by ingestion. Used as a solvent and to make paints and varnish.


2-Butoxyethanol is sensitive to air and light. Slightly soluble in water.


ETHYLENE GLYCOL N-BUTYL ETHER may react with bases, aluminum and oxidizing materials. 2-Butoxyethanol is liable to form peroxides on exposure to air and light. 2-Butoxyethanol attacks some forms of plastics, rubber and coatings. .


A toxic material. Eye and upper respiratory tract irritant. Questionable carcinogen.


2-Butoxyethanol is present in a variety of consumer products, including cleaning agents and surface coatings, such as paints, lacquers, and varnishes. 2-Butoxyethanol is readily absorbed following inhalation, oral, and dermal exposure. 2-Butoxyethanol is released into air or water by different industrial activities and facilities that manu facture, process, or use the chemical. Exposure to 2-butoxyethanol causes irritating effects to the eyes and skin, but it has not induced skin sensitization in guinea pigs. Information on the human health effects associated with exposure to 2-butoxyethanol is limited. However, case studies of individuals who had attempted suicide by ingest ing 2-butoxyethanol-containing cleaning solutions suffered poisoning with symp toms such as hemoglobinuria, erythropenia, and hypotension, metabolic acidosis, shock, non-cardiogenic pulmonary edema, and albuminuria, hepatic disorders and hematuria.


Combustible material: may burn but does not ignite readily. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form.


Reactivity with Water No reaction; Reactivity with Common Materials: No reaction; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.


Poison by ingestion, skin contact, intraperitoneal, and intravenous routes. Moderately toxic via inhalation and subcutaneous routes. Human systemic effects by inhalation: nausea or vomiting, headache, unspecified eye effects. Experimental teratogenic and reproductive effects. A skin irritant. Combustible liquid when exposed to heat or flame. To fight fire, use foam, CO2, dry chemical. Incompatible with oxidizing materials, heat, and flame. When heated to decomposition it emits acrid smoke and irritating fumes


2-Butoxy ethanol is a colorless liquid with a mild, ether like odor. Molecular weight 5 118.20; Specific gravity (H2O:1) 5 0.90; boiling point 5 171C; freezing/ melting point 5 274.8C; vapor pressure 5 0.8 mmHg @ 20C; Relative vapor density (air 5 1) 5 4.1; Flash point = 61C (cc); Autoignition temperature = 238C


Biological. Bridié et al. (1979) reported BOD and COD values of 0.71 and 2.20 g/g using filtered effluent from a biological sanitary waste treatment plant. These values were determined using a standard dilution method at 20 °C for a period of 5 d. When a sewage seed was used in a separate screening test, a BOD value of 0.20 g/g was obtained. The ThOD for 2-butoxyethanol is 2.31 g/g.
Chemical/Physical. At an influent concentration of 1,000 mg/L, treatment with GAC resulted in an effluent concentration of 441 mg/L. The adsorbability of the carbon used was 112 mg/g carbon (Guisti et al., 1974).


2-Butoxyethanol should be kept stored in tightly closed, grounded containers in a cool area with adequate ventilation, away from normal work areas and sources of heat and sparks, and electrical equipment. At the storage and handling area, workers should use solvent resistant materials.


Peroxides can be removed by refluxing with anhydrous SnCl2 or by passage under slight pressure through a column of activated alumina. Dry with anhydrous K2CO3 and CaSO4, filter and distil, or reflux with, and distil from NaOH. [Beilstein 1 IV 2380.]

Toxicity evaluation

The principal toxicological effect observed upon overexposure to EGBE is the destruction of red blood cells (RBCs) (i.e., hemolysis). BAA, the predominant oxidative metabolite of EGBE, appears responsible for this hemolytic activity. It has been speculated that BAA may interact with RBC membranes, disrupting erythrocyte osmotic balance, leading to cellular swelling, loss of deformability, and eventually hemolysis. In studies with male rats, treatment with alcohol dehydrogenase inhibitors protected against EGBE-induced hematotoxicity and inhibited EGBE metabolism to BAA. Another event in the sequelae following EGBE exposures is compensatory erythropoiesis, where as a response to the loss of erythrocytes, the bone marrow increases production of young RBCs.
In vitro studies have indicated that the RBCs of rats, mice, rabbits, and baboons are susceptible to hemolysis by BAA, whereas blood from pigs, dogs, cats, guinea pigs, and humans are resistant. A number of other studies have confirmed these results in vitro, in RBCs from a large cross-section of the human population, including those with hereditary red cell disease (i.e., sickle cell and spherocytosis) and the aged. These studies indicate that human cells are not as susceptible to hemolysis as rat cells tested under similar conditions. These findings suggest that humans exposed to equivalent doses of EGBE would not be expected to exhibit the same spectrum or severity of hematotoxic-related effects as those produced in rats. In vitro experimental results also suggest that RBCs are more sensitive to hemolysis by BAA than to hemolysis by EGBE.


May form explosive mixture with air. Can form unstable and explosive peroxides; check for peroxides prior to distillation; render harmless if positive. Decomposes, producing toxic fumes. Violent reaction with strong caustics and strong oxidizers. Attacks some coatings, plastics and rubber. Attacks metallic aluminum at high temperatures.


EGBE is destroyed by burning in an incinerator. In the laboratory, small amounts may be disposed of in the sink with a large volume of water.


Occupational workers should use minimal quantities of 2-butoxyethanol in designated areas with adequate ventilation and away from sources of heat or sparks. Whenever pos sible, fi re-resistant containers should be used. Wear appropriate protective equipment to prevent skin and eye contact.

エチレングリコールモノブチルエーテル 上流と下流の製品情報



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  • 111-76-2
  • 2-(1-butoxy)ethanol
  • 2-be
  • 2-Butossi-etanolo
  • 2-Butoxy-1-ethanol
  • 2-Butoxy-aethanol
  • 2-Butoxyethan-1-ol
  • 2-butoxy-ethano
  • 2-butoxyethanol (butyl cellosolve)
  • 2-butoxyethanol(ethyleneglycolmonobutyl
  • EthyleneglycolMonobutylEther,>99%
  • Ethylene glycol monobutyl ether(EB)
  • 2-Butoxyethanol (=butylglycol)
  • O-Butyl ethylene glycol
  • o-butylethyleneglycol
  • Poly-Solv EB
  • poly-solveb
  • 2-butoxyethanol(ethyleneglycolmonobutylether)
  • 2-Hydroxyethyl n-butyl ether
  • 3-Oxa-1-heptanol
  • 3-Oxaheptan-1-ol
  • a13-0993
  • beta-Butoxyethanol
  • BuCs
  • Butoksyetylowy alkohol
  • butoksyetylowyalkohol
  • butoksyetylowyalkohol(polish)
  • butoxyethanol(non-specificname)
  • Butyglycol
  • Butyl 2-hydroxyethyl ether
  • Butyl Cellu-Sol
  • エチレングリコールモノブチルエーテル
  • 2-ブトキシエタノール
  • ミネックスBDH
  • エクタソルブEB
  • ジェファゾールEB
  • グリコールモノブチルエーテル
  • ブチルセロソルブ
  • 2-(ブチルオキシ)エタノール
  • ガフコールEB
  • ポリソルブEB
  • 3-オキサ-1-ヘプタノール
  • モノブチルグリコールエーテル
  • ブチルセルソル
  • (2-ヒドロキシエチル)ブチルエーテル
  • キメックNR
  • β-ブトキシエタノール
  • グリコールブチルエーテル
  • O-ブチルエチレングリコール
  • エチレングリコールブチルエーテル
  • ドワノールEB
  • ブチルオキトール
  • 2-ブトキシエタノ-ル
  • 2-N-ブトキシエタノール
  • N-ブチルセロソルブ
  • エチレングリコールモノ-N-ブチルエーテル
  • 2ブトキシエタノル
  • ブトキシエタノール
  • n-ブチルセロソルブ(2-n-ブトキシエタノール)
  • ブチルグリコール
  • エチレングリコールモノ‐ノルマル‐ブチルエーテル
  • 2‐N‐ブトキシエタノール
  • エチレングリコールブチルエーテル ≥99%
  • エチレングリコールモノ-N-ブチルエーテル 2-ブトキシエタノールブチルセロソルブ
  • 2-n-ブトキシエタノール, 99%
  • 構造分類
  • 一置換エチレングリコール
  • エチレングリコール & 一置換エチレングリコール
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