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ジケテン

Diketene

HCID 12661
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基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
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基本情報

CAS
674-82-8
標準SMILES
C=C1CC(=O)O1
InChIKey
WASQWSOJHCZDFK-UHFFFAOYSA-N
分子式
C4H4O2
平均分子量
84.07 g/mol
単同位体質量
84.02112937

概要

Diketene, stabilized appears as a colorless liquid with a disagreeable odor. Slightly less dense than water. Irritates skin and eyes. Used to make paints and pharmaceuticals.

名称と識別子

優先名称
Diketene
IUPAC
4-methylideneoxetan-2-one
現地名
ジケテン
英語名
Acetyl ketene
分子式
C4H4O2
分子量
84.07

名称と別名

Diketene674-82-84-Methylene-2-oxetanone2-Oxetanone, 4-methylene-Ketene, dimer3-Buteno-beta-lactoneVinylaceto-beta-lactone0DZ97C3Z7D3-Butenoic acid, 3-hydroxy-, beta-lactoneNSC-93783DTXSID9027289RefChem:134103
名称をさらに表示
ジケテン4-メチリデンオキセタン-2-オンケテンダイマー1-ブテン-1,3-ジオン1-アセチルケテンアセチルケテン4-メチレンオキセタン-2-オンケテン,二量体ケテン二量体(ジケテン)4‐メチリデンオキセタン‐2‐オンDKAcety ketene3-hydroxy-3-butenoicacibeta-lactoneDM2-SmeDikiteneDiketenete
DTXCID107289211-617-1Acetyl ketene4-methylideneoxetan-2-one4-methyleneoxetan-2-oneEthenone, dimerKetene dimerDiketen

データベース識別子

CAS
674-82-8
PubChem CID
12661
DTXSID
DTXSID9027289
UNII
0DZ97C3Z7D
EC Number
211-617-1
Nikkaji
J1.226B

物性

構造計算による物性補完中

XLogP
0.3
極性表面積
26.3 Ų
水素結合供与体数
0
水素結合受容体数
2
回転可能結合数
0
重原子数
6
形式電荷
0
複雑度
104

実験および物理化学的性質

Chemical Classes · 2 件

Toxic Gases & Vapors -> Other Toxic Gases & Vapors

Flammable agents - 3rd degree

SpringerMaterials PropertiesBoiling point
OdorPungent odor
Density · 4 件

1.0877 g/cu cm at 20 °C

Density (at 20 °C): 1.09 g/cm³

Relative density of the vapour/air-mixture at 20 °C (air = 1): 1.02

1.0877 @ 20°C

Viscosity0.88 mPa.s
Color/Form · 3 件

Colorless liquid; turns brownish-yellow upon standing at room temperature

Colorless liquid when pure

Light colored liquid

Solubility · 5 件

Very slightly soluble in water in which it decomposes slowly

Miscible with most organic solvents. Miscible with hexane

Slightly soluble in aliphatic hydrocarbons such as hexane (ca. 12.5 wt% at 23 °C), octane, cyclohexane, and methyl cyclohexane

Soluble in common organic solvents

Solubility in water at 25 °C: slowly hydrolyzes

Flash Point · 6 件

93 °F (NFPA, 2010)

安全と法規制

安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。

GHS分類

GHS Classification · 6 件

Warning

H226: Flammable liquid and vapor [Warning Flammable liquids]

P210, P233, P240, P241, P242, P243, P261, P271, P280, P303+P361+P353, P304+P340, P317, P370+P378, P403+P235, and P501 (click each P-code to see the statement)

Danger

H226 (100%): Flammable liquid and vapor [Warning Flammable liquids]

P210, P233, P240, P241, P242, P243, P260, P261, P264, P264+P265, P270, P271, P280, P284, P301+P317, P302+P352, P303+P361+P353, P304+P340, P305+P354+P338, P316, P317, P319, P320, P321, P330, P332+P317, P362+P364, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)

危険有害性情報

Hazards IdentificationToxic/poison by inhalation (TIH/PIH)
Regulatory Information · 4 件

Chemical: 2-Oxetanone, 4-methylene-

2-Oxetanone, 4-methylene- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 2-Oxetanone, 4-methylene- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

Status: Active Update: 03-08-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/17016

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

DOT LabelPoison Inhalation Hazard Flammable Liquid
Fire Hazards · 3 件

Excerpt from ERG Guide 131 [Flammable Liquids - Toxic; polymerization hazard]:

· HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames.

Flammable. Above 33 °C explosive vapour/air mixtures may be formed. Risk of fire and explosion on contact with acids, bases or water.

Fire Potential

化学と産業

用途と製造

Uses · 4 件

Used to manufacture paints and pharmaceuticals; [CAMEO]

Reagent in synthetic organic chemistry.

Production of acetoarylamides, pigments and toners, pesticides, food preservatives, pharmaceutical intermediates.

Diketene is a powerful bactericidal agent and can raise the octane rating of gasoline [84], but is not used for these purposes in the Western hemisphere.

U.S. Production · 4 件

2023: <75,000 lb

(1972) GREATER THAN 1.36X10+6 GRAMS

(1975) GREATER THAN 4.54X10+5 GRAMS

Non-confidential 2016 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Diketene:

Methods of Manufacturing · 4 件

Ketene possesses a considerable tendency to polymerize. Under controlled conditions and in the appropriate dimerization medium, ketene can be dimerized to diketene, with yields of up to 85%, based on acetic acid. The remaining 15 % is made up by higher ketene oligomers. The preferred dimerization medium is diketene itself. Crude diketene, containing 3-4% acetic anhydride, is a mobile, dark brown liquid due to 8-10% higher polymers. Diketene of > 99.5% purity can be obtained by distillation. Ultrapure diketene (99.99%) can be obtained by crystallization.

After removal of water, acetic acid and acetic anhydride, crude ketene gas is dimerized to diketene by absorbing ketene preferably in a liquid seal pump using diketene as sealing medium. When dissolved, ketene readily dimerizes to diketene. Using controlled conditions, yields of up to 85% can be achieved based on the acetic acid feed initially used in the ketene process. The obtained crude diketene consists of a mobile, dark brown liquid, containing about 5 to 10% of triketene besides small quantities of acetic anhydride (3-4%) and higher polymers. This crude product is then fractionated over a distillation column, typically yielding diketene with more than 99.5% content. In some cases, the crude diketene can be used directly in subsequent processes. If ultra-pure diketene with a content of 99.99% is required, the distilled diketene can be crystallized from ethyl acetate or ethyl acetate and cyclohexane

Preparation from dimerization of ketene.

By spontaneous polymerization of ketene obtained by thermal decomposition of acetone or from bromoacetylbromide and zinc.

関連反応

610 件
反応記録を作成
HRID 4702 の反応式
HRID 4702溶媒としてuspto-grants-1988_02
HRID 21861 の反応式
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HRID 27907 の反応式
HRID 27907反応物としてuspto-grants-1980_09
HRID 28493 の反応式
HRID 28493反応物としてuspto-grants-2008_09
HRID 35640 の反応式
HRID 35640反応物としてuspto-grants-1988_08
HRID 46463 の反応式
HRID 46463反応物としてuspto-grants-1979_11
HRID 60339 の反応式
HRID 60339反応物としてuspto-grants-2016_09
HRID 64726 の反応式
HRID 64726反応物としてuspto-grants-1986_09
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化合物ノート

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90 °F

93.2 °F (34 °C) - closed cup

93 °F (33.9 °C) - open cup

93 °F (34 °C) - closed cup

33 °C c.c.

Boiling Point · 3 件

127 °C

127 °C

126.1 °C @760 [mm Hg]

Decomposition · 3 件

Decomposes in water.

When heated to decomposition it emits acrid smoke and fumes.

Begins to react and decompose exothermically at 208 °F (98 °C) or lower if contaminated.

Melting Point · 4 件

-6.5 °C

Heat of Fusion at Melting Point = 1.44X10+7 Joules kmol

-7 °C

-6.5 °C

Vapor Density · 2 件

2.9 (Air = 1)

Relative vapor density (air = 1): 2.9

物理化学的性質

融点
-7.5 °C · -7.5°C
沸点
69 · 69-70 °C100 mm Hg(lit.)
比重(密度)
1.09 g/mL · 1.09 g/mL at 25 °C(lit.)
蒸気密度
2.9 · 2.9 (vs air)
蒸気圧
7.9 mm · 7.9 mm Hg ( 20 °C)
屈折率
20 · n20/D 1.439(lit.)
闪点
95 °F · 95 °F
貯蔵温度
2 · 2-8°C
Henry's Law Constant
1.6 · 1.6×10-2 mol/(m3Pa) at 25℃, HSDB (2015)
InChI
InChI=1S/C4H4O2/c1-3-2-4(5)6-3/h1-2H2
InChIKey
WASQWSOJHCZDFK-UHFFFAOYSA-N
SMILES
O1C(=C)CC1=O
CAS データベース
674 · 674-82-8(CAS DataBase Reference)
NISTの化学物質情報
2 · 2-Oxetanone, 4-methylene-(674-82-8)
EPAの化学物質情報
Diketene (674-82-8)
· 3 件

Flammable.

... Moderate fire risk.

Flammable when exposed to heat or flame ... .

Health Hazards · 2 件

Excerpt from ERG Guide 131 [Flammable Liquids - Toxic; polymerization hazard]:

· TOXIC; may be fatal if inhaled, ingested or absorbed through skin.

Hazards SummaryA skin and eye irritant; [CAMEO] Inhalation may cause acute pulmonary edema; [ICSC] Diketene, stabilized (UN2521) has warning of explosive polymerization; [ERG 2016] A severe lachrymator--see Ketene in CAMEO;
DOT ID and Guide2521 131P
Reactive GroupEsters, Sulfate Esters, Phosphate Esters, Thiophosphate Esters, and Borate Esters
UN ClassificationUN Hazard Class: 6.1; UN Subsidiary Risks: 3; UN Pack Group: I
Reactivity AlertsHighly Flammable
Reactivity Profile · 1 件

DIKETENE is a very reactive dimer, it may undergo a spontaneous decomposition followed by explosion or ignition [Vervalin, 1973, p.86]. In the presence of bases, amines, mineral acids or Lewis acids a violent polymerization will occur, accompanied by gas evolution [Zdenek, F. et al., Czech Pat. 156 584, 1975].

安全と保護具

Fire Fighting · 2 件

Excerpt from ERG Guide 131 [Flammable Liquids - Toxic; polymerization hazard]:

Use carbon dioxide, dry sand. NO hydrous agents. NO water. In case of fire: keep drums, etc., cool by spraying with water. NO direct contact with water.

First Aid Measures · 4 件

Fresh air, rest. Refer for medical attention.

Remove contaminated clothes. Rinse skin with plenty of water or shower. Refer for medical attention if skin irritation occurs.

First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.

Rinse mouth. Give one or two glasses of water to drink. Refer for medical attention .

Accidental Release Measures · 2 件

· CALL 911. Then call emergency response telephone number on shipping paper. If shipping paper not available or no answer, refer to appropriate telephone number listed on the inside back cover.

· ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.

First Aid · 2 件

Excerpt from ERG Guide 131 [Flammable Liquids - Toxic; polymerization hazard]:

General First Aid:

Safe StorageSeparated from acids, bases and food and feedstuffs. Well closed. Fireproof. Cool. Dry. Store only if stabilized.
Firefighting HazardsVapors are heavier than air and may travel to a source of ignition and flash back. Closed containers may rupture violently when heated. Thermally unstable.
Exposure Control and Personal Protection · 2 件

· Wear positive pressure self-contained breathing apparatus (SCBA).

TIH (Toxic Inhalation Hazard) - Term used to describe gases and volatile liquids that are toxic when inhaled. Some are TIH materials themselves, e.g., chlorine, and some release TIH gases when spilled in water, e.g., chlorosilanes. [ERG 2016].

Fire Fighting Procedures · 3 件

To fight fire, use alcohol foam.

Approach fire from upwind to avoid hazardous vapors and toxic decomposition products. Fight fire from protected location or maximum possible distance. Use water spray to keep fire-exposed containers cool. Use flooding quantities of water as fog or spray. Carbon dioxide may be used. Extinguish fire using agent suitable for surrounding fire.

If material on fire or involved in fire: Do not extinguish fire unless flow can be stopped. Use water in flooding quantities as fog. Solid streams of water may be ineffective. Cool all affected containers with flooding quantities of water. Apply water from as far a distance as possible. Use "alcohol" foam, dry chemical or carbon dioxide. Keep run-off water out of sewers and water sources. /Diketene, stabilized/

Storage ConditionsStore at 32 °F (0 °C) in a standard flammable liquids storage warehouse, room, or cabinet. Special vented containers may be required. Separate from oxidizing materials, acids, and alkalies.
Cleanup Methods · 4 件

Environmental considerations - land spill: Dig a pit, pond, lagoon, holding area to contain liquid or solid material. /SRP: If time permits, pits, ponds, lagoons, soak holes, or holding areas should be sealed with an impermeable flexible membrane liner./ Dike surface flow using soil, sand bags, foamed polyurethane, or foamed concrete. Absorb bulk liquid with fly ash, cement powder, or commrcial sorbents. /Diketene, stabilized/

Environmental considerations - water spill: Use natural barriers or oil spill control booms to limit spill travel. Remove trapped material with suction hoses. /Diketene, stabilized/

Environmental considerations - air spill: Apply water spray or mist to knock down vapors. Disperse vapors using fans or blowers. /Diketene, stabilized/

Wear special protective clothing and positive pressure self-contained breathing apparatus. Eliminate all ignition sources. Approach release from upwind. Use water spray to cool and disperse vapors, protect personnel, and dilute spills to form nonflammable mixtures. Stop or control the leak, if this can be done without undue risk. Control runoff and isolate discharged material for proper disposal. Releases may require isolation or evacuation.

Nonfire Spill ResponseExcerpt from ERG Guide 131 [Flammable Liquids - Toxic; polymerization hazard]:
Disposal Methods · 1 件

SRP: Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in air, soil or water; effects on animal, aquatic and plant life; and conformance with environmental and public health regulations. If it is possible or reasonable use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination.

毒性情報

Ecotoxicity ValuesEC50; Species: Daphnia magna (Water flea) neonate; Conditions: freshwater, static; Concentration: 5 mg/L for 1 hr; Effect: biochemistry, fluorescence /formulation/
Environmental Fate · 3 件

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 6(SRC), determined from a structure estimation method(2), indicates that acetyl ketene is expected to have very high mobility in soil(SRC). Volatilization of acetyl ketene from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 6.1X10-4 atm-cu m/mole(SRC), developed using a fragment constant estimation method(2). Acetyl ketene is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 10.7 mm Hg at 25 °C(3). Utilizing the Japanese MITI test, 94% of the Theoretical BOD was reached in 4 weeks(4) indicating that biodegradation is an important environmental fate process in soil(SRC).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 6(SRC), determined from a structure estimation method(2), indicates that acetyl ketene is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is expected(3) based upon an estimated Henry's Law constant of 6.1X10-4 atm-cu m/mole(SRC), developed using a fragment constant estimation method(2). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 4 hrs and 4 days, respectively(SRC). According to a classification scheme(4), an estimated BCF of 3(SRC), from an estimated log Kow of -0.39(2) and a regression-derived equation(2), suggests the potential for bioconcentration in aquatic organisms is low(SRC). Utilizing the Japanese MITI test, 94% of the Theoretical BOD was reached in 4 weeks(5) indicating that biodegradation is an important environmental fate process in water(SRC).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), acetyl ketene, which has a vapor pressure of 10.7 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase acetyl ketene is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 7.5 hrs(SRC), calculated from its rate constant of 5.2X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). Vapor-phase acetyl ketene is degraded in the atmosphere by reaction with ozone(SRC); the half-life for this reaction in air is estimated to be 24 hrs(SRC), calculated from its rate constant of 1.1X10-17 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). Acetyl ketene contains chromophores that absorb at wavelengths >290 nm(4) and, therefore, may be susceptible to direct photolysis by sunlight(SRC).

Adverse EffectsDermatotoxin - Skin burns.
Exposure RoutesThe substance can be absorbed into the body by inhalation of its vapour and by ingestion.
Toxicity Summary · 1 件

IDENTIFICATION AND USE: Acetyl ketene is a colorless liquid, which turns brownish-yellow upon standing at room temperature. It is used in the production of acetoarylamides, pigments and toners, pesticides, food preservatives, pharmaceutical intermediates. It is also used as a reagent in synthetic organic chemistry. HUMAN STUDIES: There are no data available. ANIMAL STUDIES: it was not carcinogenic in mice following dermal application or sc injection, and in rats after sc injection. Extended toxicity testing on mice, rats, guinea pigs and rabbits showed that ten minute exposures to concentrations of freshly generated acetyl ketene as low as 116 ppm was lethal.

Signs and Symptoms · 4 件

Cough. Sore throat.

Redness. Pain.

Redness. Pain.

See Inhalation.

Soil Adsorption/Mobility · 1 件

Using a structure estimation method based on molecular connectivity indices(1), the Koc of acetyl ketene can be estimated to be 6(SRC). According to a classification scheme(2), this estimated Koc value suggests that acetyl ketene is expected to have very high mobility in soil(SRC).

Artificial Pollution Sources · 1 件

Acetyl ketene's use as a reagent in synthetic organic chemistry(1) and chemical intermediate for acetoacetic esters and acetoacetanilides, dyes, pharmaceuticals, food preservatives, and insecticides(2) may result in its release to the environment through various waste streams(SRC).

Environmental BiodegradationAEROBIC: Acetyl ketene, present at 100 mg/L, reached 94% of its theoretical BOD in 4 weeks using an activated sludge inoculum at 30 mg/L in the Japanese MITI test(1).
Environmental Bioconcentration · 1 件

An estimated BCF of 3 was calculated in fish for acetyl ketene(SRC), using an estimated log Kow of -0.39(1) and a regression-derived equation(1). According to a classification scheme(2), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC).

Volatilization from Water/Soil · 1 件

The Henry's Law constant for acetyl ketene is estimated as 6.1X10-4 atm-cu m/mole(SRC) developed using a fragment constant estimation method(1). This Henry's Law constant indicates that acetyl ketene is expected to volatilize from water surfaces(2). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as 4 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 4 days(SRC). Acetyl ketene's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Acetyl ketene is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 10.7 mm Hg(3).

Non-Human Toxicity Excerpts · 5 件

/LABORATORY ANIMALS: Chronic Exposure or Carcinogenicity/ Male Swiss-Millerton mice were painted 3 times weekly with approximately 100 mg of a 10% diketene in acetone solution per application. The entire backs of the animals were painted and the hair clipped when necessary. 4 control groups with 3 times weekly painting of benzene, acetone, benzo[a]pyrene, and no treatment were included. All tumors were excised at death and confirmed microscopically. The median survival time was 561 days. No tumors were observed.

/LABORATORY ANIMALS: Chronic Exposure or Carcinogenicity/ The backs of female ICR/Ha Swiss mice were freed of hair and applications of close to 100 mg of 10% solutions were made 3 times weekly onto the dorsal skin. Mice were individually weighed and observed regularly and their tumors were charted on appearance. At the time of death all animals were autopsied. All abnormal tissues and tumors were investigated microscopically. Diketene did not cause carcinogenic effects in this study. The lack of effect was so far seen on the rapid hydrolisis of the diketene. The application of diketene in tricaprylin, in which hydrolisis presumably is slower, yielded however also no carcinogenic effects.

/LABORATORY ANIMALS: Chronic Exposure or Carcinogenicity/ Subcutaneous injection in female Sprague-Dawley rats. 4 mg diketene in 0.1 mL tricaprylin was subcutaneously injected once weekly in the left axillary area. The rats were examined regularly for palpable masses and their condition was recorded once a month. They were treated and observed for their lifespans (543 days). No local subcutaneous sarcomas were found.

/LABORATORY ANIMALS: Chronic Exposure or Carcinogenicity/ Subcutaneous injection of diketene in mice with tricaprylin as vehicle, once weekly. 1.1 mg per injection. No tumors were observed after 20 months.

/OTHER TOXICITY INFORMATION/ Extended toxicity testing on mice, rats, guinea pigs and rabbits showed that ten minute exposures to concentrations of freshly generated ketene as low as 0.2 mg/L (116 ppm) may produce a high percentage of deaths in small animals.

法規制情報

Atmospheric Standards · 1 件

This action promulgates standards of performance for equipment leaks of Volatile Organic Compounds (VOC) in the Synthetic Organic Chemical Manufacturing Industry (SOCMI). The intended effect of these standards is to require all newly constructed, modified, and reconstructed SOCMI process units to use the best demonstrated system of continuous emission reduction for equipment leaks of VOC, considering costs, non air quality health and environmental impact and energy requirements. Diketene is produced, as an intermediate or a final product, by process units covered under this subpart.

安全データ

F
19-21-27
wgk
2
IDLA
7.6 ppm
tsca
TSCA listed
rtecs
RQ8225000
ridadr
UN 2521 (DIKETENE, STABILIZED)
PRTR法
第1種指定化学物質
hs_code
2914190090
risk_code
10-20-40-36/37/38
化審法
一般化学物質
hazard_code
Xn
safety_code
3-36/37-33-24/25-23-16-26
hazard_class
6.1
packing_group
I
有毒物質データの
674-82-8(Hazardous Substances Data)
危険度評価(NFPA 704基準/消防庁データ)
人的[青]=1 火災[赤]=3
General Manufacturing Information · 2 件

2-Oxetanone, 4-methylene-: ACTIVE

Diketene is now generally consumed at the site of production, because of its extreme reactivity and hazardous properties.

応用分野 · 4 件

解説ジケテン,放置すると徐々に重合するため,安定剤を含んだ形で販売されることもある.550 ℃ 程度で熱分解するとアセチル化剤などとして有用なケテンを生成する.また,さまざまな求核体(アルコール,アミンなど)と反応し,アセト酢酸誘導体を生成する.この性質を利用してアミノ基などの保護基として用いられることもある.求電子体とはエキソメチレン部で反応し,4位に置換基をもつアセトアセチル誘導体を与える.LD50 560 mg/kg(ラット,経口).森北出版「化学辞典(第2版)

用途医薬、染料、防腐剤原料

使用Diketene is used as a reactant in the manufacture of paper and control of its sizing. In addition its used in the preparation of potent and selective inhibitor of histone methyltransferase EZH2 in the treatment of B-Cell lymphomas.

一般的な説明A colorless liquid with a disagreeable odor. Slightly less dense than water. Flash point 90°F. Irritates skin and eyes. Used to make paints and pharmaceuticals.

上流・下流製品情報

上流原料

りん酸 トリエチルアセトンPolymerization inhibitorポリエチレン酢酸ブチル酢酸ケテン

下流製品

デヒドロ酢酸アセト酢酸エチルN,N'-ビス(アセトアセチル)-o-トルイジンアセト酢酸tert-ブチルアセトアセトアニリドアセト酢酸(2E)-3,7-ジメチル-2,6-オクタジエニル22(S),23(S)-Homobrassinolide4-オキソ-6-メチル-3,4-ジヒドロ-1,2,3-オキサチアジン2,2-ジオキシドアミトリプチリン 塩酸塩3-メチル-1-フェニル-5-ピラゾロン酪酸無水物3-オキソブチルアミドソルビン酸p-アセトアセトアニシジド4-クロロアセト酢酸エチルオラキンドクス無水酢酸アセスルファムKN,N-ジエチルアセトアセタミド5-Chloro-6 b,19-epoxy-5a -androtane-3,17-dione1,4-ジヒドロ-2,6-ジメチル-4-(3-ニトロフェニル)-3,5-ピリジンジカルボン酸3-[2-[4-(ジフェニルメチル)ピペラジン-1-イル]エチル]5-メチルアセト酢酸メチルPigment Red 122N-アセトアセチル-o-トルイジンクロロアセチルクロリド1-(2',5'-ジクロロ-4'-スルホフェニル)-3-メチル-5-ピラゾロンo-アセトアセトアニシジドりん酸ジメチル[3-(ジエチルアミノ)-3-オキソ-2-クロロ-1-メチル-1-プロペニル]Seedavay(Uniroyal)α-アセチル-γ-ブチロラクトンN-Acetyl-N-(4-chloro-2-nitrophenyl)acetamideN-メチルアセトアセトアミド (約70%水溶液)2,6-ヘプタンジオンキザロホップ-P-エチル標準品アセト酢酸ブチル2-[4,5-ジヒドロ-4-メチル-4-イソプロピル-5-オキソ-1H-イミダゾール-2-イル]-5-エチル-3-ピリジンカルボン酸アセト酢酸イソブチル2'-クロロアセトアセトアニリド