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2,4-己二酮 | 3002-24-2

中文名称
2,4-己二酮
中文别名
二环[4.3.0]-1,5-二氮-5-十一烯;偶氮二异丁脒盐酸盐
英文名称
hexane-2,4-dione
英文别名
2,4-hexanedione;3-methyl-acetylacetone
2,4-己二酮化学式
CAS
3002-24-2
化学式
C6H10O2
mdl
MFCD00009318
分子量
114.144
InChiKey
NDOGLIPWGGRQCO-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    240-241℃
  • 沸点:
    161℃
  • 密度:
    0.936±0.06 g/cm3 (20 ºC 760 Torr)
  • 闪点:
    53.6±16.8℃
  • LogP:
    0.779 (est)
  • 保留指数:
    862

计算性质

  • 辛醇/水分配系数(LogP):
    0.3
  • 重原子数:
    8
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.666
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 危险等级:
    3.2
  • 海关编码:
    2914190090
  • 包装等级:
    III
  • 危险类别:
    3.2
  • 危险品运输编号:
    UN 1224
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H225,H315,H319,H335
  • 储存条件:
    | 2-8°C |

SDS

SDS:fec0742e7981d5b47f8b9477f7cd38b7
查看
Name: 2 4-Hexanedione 99 % (GC) Material Safety Data Sheet
Synonym: Propionylacetone
CAS: 3002-24-2
Section 1 - Chemical Product MSDS Name:2 4-Hexanedione 99 % (GC) Material Safety Data Sheet
Synonym:Propionylacetone

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
3002-24-2 2,4-Hexanedione 99 221-094-1
Hazard Symbols: XI
Risk Phrases: 10 36/37/38

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Flammable. Irritating to eyes, respiratory system and skin.
Potential Health Effects
Eye:
Causes eye irritation. May cause chemical conjunctivitis and corneal damage.
Skin:
Causes skin irritation. May cause irritation and dermatitis. May cause cyanosis of the extremities.
Ingestion:
May cause gastrointestinal irritation with nausea, vomiting and diarrhea. The toxicological properties of this substance have not been fully investigated. Ingestion of large amounts may cause CNS depression.
Inhalation:
Causes respiratory tract irritation. The toxicological properties of this substance have not been fully investigated. Aspiration may lead to pulmonary edema. Vapors may cause dizziness or suffocation. Can produce delayed pulmonary edema. May cause burning sensation in the chest.
Chronic:
Effects may be delayed.

Section 4 - FIRST AID MEASURES
Eyes: Immediately flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Get medical aid.
Skin:
Get medical aid. Flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes. Wash clothing before reuse.
Ingestion:
Get medical aid. Do NOT induce vomiting. If conscious and alert, rinse mouth and drink 2-4 cupfuls of milk or water.
Inhalation:
Remove from exposure and move to fresh air immediately. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Get medical aid.
Notes to Physician:
Treat symptomatically and supportively.

Section 5 - FIRE FIGHTING MEASURES
General Information:
As in any fire, wear a self-contained breathing apparatus in pressure-demand, MSHA/NIOSH (approved or equivalent), and full protective gear. Vapors may form an explosive mixture with air.
Vapors can travel to a source of ignition and flash back. During a fire, irritating and highly toxic gases may be generated by thermal decomposition or combustion. Will burn if involved in a fire. Use water spray to keep fire-exposed containers cool. Water may be ineffective. Material is lighter than water and a fire may be spread by the use of water. Containers may explode in the heat of a fire.
Flammable liquid and vapor. Vapors may be heavier than air. They can spread along the ground and collect in low or confined areas.
Extinguishing Media:
For small fires, use dry chemical, carbon dioxide, water spray or alcohol-resistant foam. For large fires, use water spray, fog, or alcohol-resistant foam. Use water spray to cool fire-exposed containers. Water may be ineffective. Do NOT use straight streams of water.

Section 6 - ACCIDENTAL RELEASE MEASURES
General Information: Use proper personal protective equipment as indicated in Section 8.
Spills/Leaks:
Absorb spill with inert material (e.g. vermiculite, sand or earth), then place in suitable container. Avoid runoff into storm sewers and ditches which lead to waterways. Clean up spills immediately, observing precautions in the Protective Equipment section. Remove all sources of ignition. Use a spark-proof tool. Provide ventilation. A vapor suppressing foam may be used to reduce vapors.

Section 7 - HANDLING and STORAGE
Handling:
Wash thoroughly after handling. Remove contaminated clothing and wash before reuse. Use with adequate ventilation. Ground and bond containers when transferring material. Use spark-proof tools and explosion proof equipment. Avoid contact with eyes, skin, and clothing. Empty containers retain product residue, (liquid and/or vapor), and can be dangerous. Keep container tightly closed. Keep away from heat, sparks and flame. Avoid ingestion and inhalation. Do not pressurize, cut, weld, braze, solder, drill, grind, or expose empty containers to heat, sparks or open flames.
Storage:
Keep away from heat, sparks, and flame. Keep away from sources of ignition. Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.
Flammables-area.

Section 8 - EXPOSURE CONTROLS, PERSONAL PROTECTION
Engineering Controls:
Facilities storing or utilizing this material should be equipped with an eyewash facility and a safety shower. Use adequate general or local explosion-proof ventilation to keep airborne levels to acceptable levels.
Exposure Limits CAS# 3002-24-2: Personal Protective Equipment Eyes: Wear appropriate protective eyeglasses or chemical safety goggles as described by OSHA's eye and face protection regulations in 29 CFR 1910.133 or European Standard EN166.
Skin:
Wear appropriate protective gloves to prevent skin exposure.
Clothing:
Wear appropriate protective clothing to prevent skin exposure.
Respirators:
A respiratory protection program that meets OSHA's 29 CFR 1910.134 and ANSI Z88.2 requirements or European Standard EN 149 must be followed whenever workplace conditions warrant respirator use.

Section 9 - PHYSICAL AND CHEMICAL PROPERTIES

Physical State: Liquid
Color: colorless
Odor: acetone-like
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: 152 - 154 deg C @ 760.00mm Hg
Freezing/Melting Point: Not available.
Autoignition Temperature: Not available.
Flash Point: 46 deg C ( 114.80 deg F)
Explosion Limits, lower: Not available.
Explosion Limits, upper: Not available.
Decomposition Temperature:
Solubility in water:
Specific Gravity/Density: .9590g/cm3
Molecular Formula: C6H10O2
Molecular Weight: 114.14

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Stable at room temperature in closed containers under normal storage and handling conditions.
Conditions to Avoid:
Incompatible materials, ignition sources, excess heat, strong oxidants.
Incompatibilities with Other Materials:
Oxidizing agents.
Hazardous Decomposition Products:
Carbon monoxide, irritating and toxic fumes and gases, carbon dioxide.
Hazardous Polymerization: Has not been reported

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 3002-24-2: MO3145000 LD50/LC50:
Not available.
Carcinogenicity:
2,4-Hexanedione - Not listed by ACGIH, IARC, or NTP.
Other:
See actual entry in RTECS for complete information.

Section 12 - ECOLOGICAL INFORMATION


Section 13 - DISPOSAL CONSIDERATIONS
Dispose of in a manner consistent with federal, state, and local regulations.

Section 14 - TRANSPORT INFORMATION

IATA
Shipping Name: KETONES, LIQUID, N.O.S.*
Hazard Class: 3
UN Number: 1224
Packing Group: III
IMO
Shipping Name: KETONES, LIQUID, N.O.S.
Hazard Class: 3.3
UN Number: 1224
Packing Group: III
RID/ADR
Shipping Name: KETONES, N.O.S.
Hazard Class: 3
UN Number: 1224
Packing group: III

Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: XI
Risk Phrases:
R 10 Flammable.
R 36/37/38 Irritating to eyes, respiratory system
and skin.
Safety Phrases:
S 9 Keep container in a well-ventilated place.
S 16 Keep away from sources of ignition - No
smoking.
S 24/25 Avoid contact with skin and eyes.
S 28A After contact with skin, wash immediately with
plenty of water.
S 33 Take precautionary measures against static
discharges.
S 37 Wear suitable gloves.
S 45 In case of accident or if you feel unwell, seek
medical advice immediately (show the label where
possible).
WGK (Water Danger/Protection)
CAS# 3002-24-2: No information available.
Canada
CAS# 3002-24-2 is listed on Canada's DSL List.
CAS# 3002-24-2 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 3002-24-2 is listed on the TSCA inventory.


SECTION 16 - ADDITIONAL INFORMATION
N/A

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2,4-己二酮4-乙酰氨基苯磺酰叠氮 作用下, 以 乙腈 为溶剂, 以93%的产率得到(2Z)-3-偶氮基-4-氧代-2-戊烯-2-醇
    参考文献:
    名称:
    基于双氧化[3 + 3]环加成反应的二氢吡喃并[4,3-b]吲哚的电合成。
    摘要:
    氧化性[3 + 3]环加成反应为六元环形成提供了一条有效途径。该方法是基于吲哚/烯胺与活性亚甲基化合物的电化学氧化偶联,然后串联6π-电环化反应生成二氢吡喃并[4,3- b ]吲哚和2,3-二氢呋喃而实现的。阳极氧化产生的自由基与自由基从O 2产生的自由基之间的自由基交叉偶联为合成结构复杂的杂环提供了温和的反应条件。
    DOI:
    10.1002/anie.202003364
  • 作为产物:
    描述:
    2,4-己二炔甲醇硫酸 、 mercury(II) sulfate 作用下, 生成 2,4-己二酮
    参考文献:
    名称:
    Mkrjan; Papasjan, Doklady Akademii Nauk Armyanskoi SSR, 1953, vol. 16, p. 103,105
    摘要:
    DOI:
  • 作为试剂:
    描述:
    哌啶5-氨基四氮唑2,4-己二酮乙醇 作用下, 生成 5,6,7-trimethyl-tetrazolo[1,5-a]pyrimidine
    参考文献:
    名称:
    Buelow, Chemische Berichte, 1909, vol. 42, p. 4434
    摘要:
    DOI:
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文献信息

  • [EN] TRICYCLIC COMPOUNDS AS ALLOSTERIC MODULATORS OF METABOTROPIC GLUTAMATE RECEPTORS<br/>[FR] COMPOSÉS TRICYCLIQUES COMME MODULATEURS ALLOSTÉRIQUES DES RÉCEPTEURS MÉTABOTROPES AU GLUTAMATE
    申请人:MERCK SHARP & DOHME
    公开号:WO2012006760A1
    公开(公告)日:2012-01-19
    The present invention describes and claims compounds of the Structural Formula (I), Structural Formula (II), or Structural Formula (III). In Formula (I), R1, R2, R3 and R3' are -H or methyl, or R3 and R3' taken together form a double bond, or R3' is -H and R2 and R3 taken together form a spiro-cyclopropyl substituent, R4 is -H or -F, and R5 is -H, methyl, -Cl or -Br. In Formula (II), R1 is -H, ethyl-, isopropyl-, cyclopropyl-, methyl- or methoxy-, R4 is -H or -F, and "Y" is: (a) -CH2-; (b) -CR6H-O-CR7R8-, wherein R6, R7, and R8 are independently -H or methyl; (c) -CR6H-N(R9)-CR7R8-, wherein R6, R7, and R8 are independently -H or methyl; (d) -CH2-C(R9)(R10)-C(R7)(R8)-, wherein R7, R8, R9 and R10 are independently -H or -methyl, or both R7 and R8 are -F, R9 and R10 are independently -H or -methyl, or both R9 and R10 are -F, or R9 and R10 taken together are (O=), which together with the carbon to which they are attached forms a carbonyl group.
    本发明描述和声明了结构式(I)、结构式(II)或结构式(III)的化合物。在结构式(I)中,R1、R2、R3和R3'为-H或甲基,或R3和R3'一起形成双键,或R3'为-H且R2和R3一起形成螺环丙基取代基,R4为-H或-F,R5为-H、甲基、-Cl或-Br。在结构式(II)中,R1为-H、乙基、异丙基、环丙基、甲基或甲氧基,R4为-H或-F,“Y”为:(a)-CH2-;(b)-CR6H-O-CR7R8-,其中R6、R7和R8独立地为-H或甲基;(c)-CR6H-N(R9)-CR7R8-,其中R6、R7和R8独立地为-H或甲基;(d)-CH2-C(R9)(R10)-C(R7)(R8)-,其中R7、R8、R9和R10独立地为-H或-甲基,或R7和R8都为-F,R9和R10独立地为-H或-甲基,或R9和R10都为-F,或R9和R10一起为(O=),与它们连接的碳一起形成羰基。
  • Composition and Method for Producing ITO Powders or ITO Coatings
    申请人:Bubel Carsten
    公开号:US20120070690A1
    公开(公告)日:2012-03-22
    A composition for preparing ITO powders and ITO coatings includes at least one indium compound and at least one bimetal compound which includes indium and tin. A method of preparing ITO powders and ITO coatings includes a one-step temperature treatment in an inert atmosphere.
    一种用于制备ITO粉末和ITO涂层的组合物包括至少一种铟化合物和至少一种含铟和锡的双金属化合物。一种制备ITO粉末和ITO涂层的方法包括在惰性气氛中进行一步温度处理。
  • HETEROCYCLIC UREA DERIVATIVES AND METHODS OF USE THEREOF
    申请人:CHOY Allison Laura
    公开号:US20100317624A1
    公开(公告)日:2010-12-16
    Compounds of formula (IA) and their pharmaceutically acceptable salts are described. Processes for their preparation, pharmaceutical compositions containing them, their use as medicaments and their use in the treatment of bacterial infections are also described.
    公式(IA)的化合物及其药用可接受的盐被描述。还描述了它们的制备过程、含有它们的药物组合物、它们作为药物的使用以及它们在治疗细菌感染中的用途。
  • [EN] HETEROCYCLIC COMPOUNDS AND THEIR USE AS RETINOID-RELATED ORPHAN RECEPTOR (ROR) GAMMA-T INHIBITORS<br/>[FR] COMPOSÉS HÉTÉROCYCLIQUES ET LEUR UTILISATION EN TANT QU'INHIBITEURS GAMMA-T DU RÉCEPTEUR ORPHELIN APPARENTÉ AUX RÉCEPTEURS DES RÉTINOÏDES (ROR) )
    申请人:TAKEDA PHARMACEUTICAL
    公开号:WO2016002968A1
    公开(公告)日:2016-01-07
    Provided are heterocyclic compounds having a RORγt inhibitory action represented by the formula (I): wherein each symbol is as defined in the specification, or a salt thereof.
    提供的是具有RORγt抑制作用的杂环化合物,其由公式(I)表示:其中每个符号如说明书中定义,或其盐。
  • A new facile, efficient synthesis and structure peculiarity of quinoxaline derivatives with two benzimidazole fragments
    作者:Vakhid A. Mamedov、Nataliya A. Zhukova、Victor V. Syakaev、Aidar T. Gubaidullin、Tat'yana N. Beschastnova、Dil'bar I. Adgamova、Aida I. Samigullina、Shamil K. Latypov
    DOI:10.1016/j.tet.2012.10.045
    日期:2013.1
    A highly efficient and versatile method for the synthesis of quinoxaline derivatives with two benzimidazole fragments have been developed on the basis of the ring contraction of 3-(benzimidazo-2-yl)quinoxalin-2(1H)-one with 1,2-diaminobenzene and its various types of substituted and condensed derivatives. Owing to the inter- and intramolecular processes, involving self association, proton exchange
    基于3-(苯并咪唑-2-基)喹喔啉-2(1 H)-与1,2-的环收缩,已开发出一种高效且通用的具有两个苯并咪唑片段的喹喔啉衍生物的合成方法。二氨基苯及其各种类型的取代和稠合衍生物。由于分子间和分子内过程,涉及桥联和相邻碳原子的大多数双-苯并咪唑基喹喔啉信号的几种形式之间的自缔合,质子交换,构象和/或互变异构交换,且NMR光谱中的苯并咪唑片段变宽。苯并咪唑片段与分子的喹喔啉核心之间的共轭作用比喹喔啉衍生物(10c)与其噻二唑[ f ]-(17)和吡咯并[ a ]-(19)环化了衍生物,导致整个分子的平面度更大。
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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mass
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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