2,2-二辛基-1,3-丙二醇 | 106868-09-1

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 中文名称: 2,2-二辛基-1,3-丙二醇
• 中文别名: 9,9-双(羟甲基)十七烷；1,3-二羟基-2,2-正辛基丙烷；2,2-二正辛基-1,3-丙二醇
• 英文名称: 2,2-di-n-octyl-1,3-propanediol
• 英文别名: 2,2-dioctyl-propane-1,3-diol；2,2-dioctyl-1,3-propanediol；2,2-dioctylpropan-1,3-diol；2,2-Dioctylpropane-1,3-diol
• CAS: 106868-09-1
• 化学式: C₁₉H₄₀O₂
• 分子量: 300.525
• InChiKey: NFPNQEAEXIXGNY-UHFFFAOYSA-N

物化性质

• 沸点：
  424.3±18.0 °C(Predicted)
• 密度：
  0.891±0.06 g/cm3(Predicted)
• 溶解度：
  溶于甲醇

计算性质

• 辛醇/水分配系数(LogP)：
  7.3
• 重原子数：
  21
• 可旋转键数：
  16
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  40.5
• 氢给体数：
  2
• 氢受体数：
  2

安全信息

• 海关编码：
  2905399090

SDS

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Section I.Chemical Product and Company Identification
Chemical Name 2,2-Di-n-octyl-1,3-propanediol
Portland OR
Synonym 1,3-Propanediol, 2,2-dioctyl -(9CI)
Chemical Formula C19H40O2
CAS Number 106868-09-1

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Section II. Composition and Information on Ingredients
Chemical Name CAS Number Percent (%) TLV/PEL Toxicology Data
2,2-Di-n-octyl-1,3-propanediol 106868-09-1 Not available. Not available. Not available.

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Section III. Hazards Identification
Acute Health Effects No specific information is available in our data base regarding the toxic effects of this material for humans. However,
exposure to any chemical should be kept to a minimum. Skin and eye contact may result in irritation. May be harmful if
inhaled or ingested. Always follow safe industrial hygiene practices and wear proper protective equipment when handling
this compound.
CARCINOGENIC EFFECTS : Not available.
Chronic Health Effects
MUTAGENIC EFFECTS : Not available.
TERATOGENIC EFFECTS : Not available.
DEVELOPMENTAL TOXICITY: Not available.
Repeated or prolonged exposure to this compound is not known to aggravate existing medical conditions.

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Section IV. First Aid Measures
Eye Contact Check for and remove any contact lenses. In case of contact, immediately flush eyes with plenty of water for at least 15
minutes. Get medical attention.
Skin Contact In case of contact, immediately flush skin with plenty of water. Remove contaminated clothing and shoes. Wash clothing
before reuse. Thoroughly clean shoes before reuse. Get medical attention.
Inhalation If the victim is not breathing, perform mouth-to-mouth resuscitation. Loosen tight clothing such as a collar, tie, belt or
waistband. If breathing is difficult, oxygen can be administered. Seek medical attention if respiration problems do not
improve.
Ingestion INDUCE VOMITING by sticking finger in throat. Lower the head so that the vomit will not reenter the mouth and throat.
Loosen tight clothing such as a collar, tie, belt or waistband. If the victim is not breathing, perform mouth-to-mouth
resuscitation. Examine the lips and mouth to ascertain whether the tissues are damaged, a possible indication that the
toxic material was ingested; the absence of such signs, however, is not conclusive.

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Section V. Fire and Explosion Data
Auto-Ignition Not available.
Flammability May be combustible at high temperature.
Flammable Limits
Flash Points Not available.
Not available.
Combustion Products These products are toxic carbon oxides (CO, CO 2).
Fire Hazards
Not available.
Risks of explosion of the product in presence of mechanical impact: Not available.
Explosion Hazards
Risks of explosion of the product in presence of static discharge: Not available.
Fire Fighting Media
SMALL FIRE: Use DRY chemical powder.
and Instructions LARGE FIRE: Use water spray, fog or foam. DO NOT use water jet.
Consult with local fire authorities before attempting large scale fire-fighting operations.
Continued on Next Page
2,2-Di-n-octyl-1,3-propanediol

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Section VI. Accidental Release Measures
Spill Cleanup Use a shovel to put the material into a convenient waste disposal container. Finish cleaning the spill by rinsing any
Instructions contaminated surfaces with copious amounts of water. Consult federal, state, and/or local authorities for assistance on
disposal.

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Section VII. Handling and Storage
Handling and Storage Keep away from heat. Mechanical exhaust required. When not in use, tightly seal the container and store in a dry, cool
place. Avoid excessive heat and light. Do not breathe dust.
Information
Always store away from incompatible compounds such as oxidizing agents.

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Section VIII. Exposure Controls/Personal Protection
Engineering Controls Use process enclosures, local exhaust ventilation, or other engineering controls to keep airborne levels below
recommended exposure limits. If user operations generate dust, fume or mist, use ventilation to keep exposure to
airborne contaminants below the exposure limit.
Personal Protection Splash goggles. Lab coat. Dust respirator. Boots. Gloves. Suggested protective clothing might not be sufficient; consult
a specialist BEFORE handling this product. Be sure to use a MSHA/NIOSH approved respirator or equivalent.
Exposure Limits Not available.

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Section IX. Physical and Chemical Properties
Solid. (White Crystal Lumps.) Solubility
Physical state @ 20°C Soluble in methanol.
Not available.
Specific Gravity
Molecular Weight 300.52 Partition Coefficient Not available.
Boiling Point
Not available. Vapor Pressure Not applicable.
Melting Point 36°C (96.8°F) Vapor Density Not available.
Refractive Index Not available. Volatility Not available.
Critical Temperature Not available. Odor Not available.
Viscosity Not available. Taste Not available.

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Section X. Stability and Reactivity Data
Stability

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This material is stable if stored under proper conditions. (See Section VII for instructions)
Conditions of Instability Avoid excessive heat and light.
Incompatibilities
Reactive with oxidizing agents.

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Section XI. Toxicological Information
RTECS Number Not available.
Eye Contact. Ingestion. Inhalation.
Routes of Exposure
Toxicity Data Not available.
Chronic Toxic Effects CARCINOGENIC EFFECTS : Not available.
MUTAGENIC EFFECTS : Not available.
TERATOGENIC EFFECTS : Not available.
DEVELOPMENTAL TOXICITY: Not available.
Repeated or prolonged exposure to this compound is not known to aggravate existing medical conditions.
Acute Toxic Effects No specific information is available in our data base regarding the toxic effects of this material for humans. However,
exposure to any chemical should be kept to a minimum. Skin and eye contact may result in irritation. May be harmful if
inhaled or ingested. Always follow safe industrial hygiene practices and wear proper protective equipment when handling
this compound.
Continued on Next Page
2,2-Di-n-octyl-1,3-propanediol

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Section XII. Ecological Information
Ecotoxicity Not available.
Environmental Fate Not available.

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Section XIII. Disposal Considerations
Recycle to process, if possible. Consult your local regional authorities. You may be able to dissolve or mix material with a
Waste Disposal
combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber system. Observe all
federal, state and local regulations when disposing of the substance.

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Section XIV. Transport Information
DOT Classification Not a DOT controlled material (United States).
PIN Number Not applicable.
Proper Shipping Name
Not applicable.
Packing Group (PG) Not applicable.
DOT Pictograms

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Section XV. Other Regulatory Information and Pictograms
TSCA Chemical Inventory This product is NOT on the EPA Toxic Substances Control Act (TSCA) inventory. The following notices are required by 40
CFR 720.36 (C) for those products not on the inventory list:
(EPA)
(i) These products are supplied solely for use in research and development by or under the supervision of a technically
qualified individual as defined in 40 CFR 720.0 et sec.
(ii) The health risks of these products have not been fully determined. Any information that is or becomes available will be
supplied on an MSDS sheet.
WHMIS Classification Not available.
(Canada)
EINECS Number (EEC) Not available.
EEC Risk Statements Not available.

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SECTION 16 - ADDITIONAL INFORMATION
N/A

反应信息

• 作为反应物：
  描述：

  2,2-二辛基-1,3-丙二醇 在 草酰氯 、 二甲基亚砜 、 三乙胺 、 氯化铵 作用下， 以 二氯甲烷 、 水 为溶剂， 反应 3.0h， 生成 2,2-di-n-octylmalonaldehyde
  参考文献：
  名称：

  前所未有的形状的自组装胶囊

  摘要：

  弯曲的宿主：描述了弯曲分子胶囊的第一个例子：它们具有香蕉或 S 形状（见图），并且能够选择性地结合互补形状的客人。

  DOI：

  10.1002/anie.201102548
• 作为产物：
  描述：

  二辛基丙二酸二乙酯 在 lithium aluminium tetrahydride 作用下， 以 乙醚 为溶剂， 以69%的产率得到2,2-二辛基-1,3-丙二醇
  参考文献：
  名称：

  双邻苯二甲腈在侧链1,11,15,25-四取代酞菁合成中的应用

  摘要：

  3-硝基邻苯二甲腈的亲核芳族取代反应产生3-羟基邻苯二甲腈和3-新戊氧基邻苯二甲腈，后者缩合为1,8,15,22-四新戊氧基酞菁作为异构体的混合物。双邻苯二甲腈，例如 1,3-双(2',3'-二氰基苯氧基)-2,2-二戊基丙烷、1,3-双(2',3'-二氰基苯氧基)-2,2-二乙基丙烷、1,3-双(2',3'-二氰基苯氧基)-2,2-二辛基丙烷和1,3-双(2',3'-二氰基苯氧基)-2-甲基-2-三苯甲氧基甲基丙烷均得到双冠状1,11， 15,25-四取代酞菁作为纯化合物，在 1-辛醇中在 196 °C 下用辛氧化锂处理。其他九种双邻苯二甲腈，包括 1,5-双(2',3'-二氰基苯氧基)-3-氧戊烷、1,1-双(2',3'-二氰基苯氧基甲基)环己烷、1,2-双(2') ,3'-二氰基苯氧基甲基)苯和 2,5-双(2', 3'-二氰基苯氧基甲基）呋喃不会二聚化为单核酞菁。“宝石二甲基”效应

  DOI：

  10.1139/v96-035

文献信息

• AMPHIPATHIC COMPOUND HAVING NOVEL PENTA-SACCHARIDE HYDROPHILIC GROUP AND USE THEREOF
  申请人：Industry-University Cooperation Foundation Hanyang University Erica Campus

  公开号：US20190169218A1

  公开（公告）日：2019-06-06

  Disclosed are an amphipathic compound having a penta-saccharide hydrophilic group, a method of preparing the same, and a method of extracting, solubilizing, stabilizing, crystallizing or analyzing membrane proteins and membrane protein complexes using the same. In particular, since the compound has a high-density penta-saccharide hydrophilic group composed of five glucose units, the compound may have an excellent effect on crystallization of membrane proteins. In addition, since the hydrophilic group used in the amphipathic compound has a novel structure, the hydrophilic group may be applied to the development of various amphipathic molecules.

  披露了一种具有戊糖水基团的亲水性化合物，其制备方法以及使用该化合物提取、溶解、稳定、结晶或分析膜蛋白和膜蛋白复合物的方法。特别是，由于该化合物具有由五个葡萄糖单位组成的高密度戊糖水基团，该化合物可能对膜蛋白结晶具有显著效果。另外，由于在两亲性化合物中使用的亲水基团具有新颖的结构，该亲水基团可应用于各种两亲性分子的开发。
• The use of bisphthalonitriles in the synthesis of side-strapped 1,11,15,25-tetrasubstituted phthalocyanines
  作者：Clifford C. Leznoff、David M. Drew

  DOI：10.1139/v96-035

  日期：1996.3.1

  25-tetrasubstituted phthalocyanines as pure compounds when treated with lithium octoxide in 1-octanol at 196 °C. A host of nine other bisphthalonitriles including 1,5-bis(2′,3′-dicyanophenoxy)-3-oxapentane, 1,1-bis(2′,3′-dicyanophenoxymethyl)cyclohexane, 1,2-bis(2′,3′-dicyanophenoxymethyl)benzene, and 2,5-bis(2′,3′-dicyanophenoxymethyl)furan did not dimerize to mononuclear phthalocynaines. The "gem dimethyl"

  3-硝基邻苯二甲腈的亲核芳族取代反应产生3-羟基邻苯二甲腈和3-新戊氧基邻苯二甲腈，后者缩合为1,8,15,22-四新戊氧基酞菁作为异构体的混合物。双邻苯二甲腈，例如 1,3-双(2',3'-二氰基苯氧基)-2,2-二戊基丙烷、1,3-双(2',3'-二氰基苯氧基)-2,2-二乙基丙烷、1,3-双(2',3'-二氰基苯氧基)-2,2-二辛基丙烷和1,3-双(2',3'-二氰基苯氧基)-2-甲基-2-三苯甲氧基甲基丙烷均得到双冠状1,11， 15,25-四取代酞菁作为纯化合物，在 1-辛醇中在 196 °C 下用辛氧化锂处理。其他九种双邻苯二甲腈，包括 1,5-双(2',3'-二氰基苯氧基)-3-氧戊烷、1,1-双(2',3'-二氰基苯氧基甲基)环己烷、1,2-双(2') ,3'-二氰基苯氧基甲基)苯和 2,5-双(2', 3'-二氰基苯氧基甲基）呋喃不会二聚化为单核酞菁。“宝石二甲基”效应
• METHOD FOR PRODUCING DIVINYL ETHER COMPOUND HAVING ALKYLENE SKELETON
  申请人：MARUZEN PETROCHEMICAL CO., LTD.

  公开号：US20220033334A1

  公开（公告）日：2022-02-03

  A method of purifying a divinyl ether compound having an alkylene skeleton may take place with low energy and in a simplified manner. Such a method for producing a divinyl ether compound may include: reacting a compound of formula (1) wherein R 1 is an alkylene group having 4 to 20 carbon atoms, with acetylene by using an alkali metal catalyst; and purifying the divinyl ether compound of formula (2) which is obtained in the reacting, without an extraction.

  一种用低能耗和简化方式进行的纯化含有烯基醚基团的烯基醚化合物的方法。生产烯基醚化合物的方法可能包括：通过使用碱金属催化剂将具有4到20个碳原子的烯基醚基团的化合物（式1）与乙炔发生反应；并在反应中获得的烯基醚化合物（式2）进行纯化，而无需提取。
• Toner and toner production method
  申请人：Canon Kabushiki Kaisha

  公开号：EP2701008A1

  公开（公告）日：2014-02-26

  The present invention provides a toner having superior color development property and a method of producing a toner having favorable particle size distribution and color development property, in which the toner containing a binder resin and a colorant that contains a phthalocyanine pigment represented by general formula (1), and the method for producing the toner.

  本发明提供了一种具有优越的色彩发展性能的调色剂以及一种制备具有良好颗粒大小分布和色彩发展性能的调色剂的方法，其中该调色剂包含一种含有通式（1）所表示的菲洛蓝素颜料的粘合剂树脂和着色剂，以及制备该调色剂的方法。
• Electrochromic polymers and polymer electrochromic devices
  申请人：University of Florida

  公开号：US20030174377A1

  公开（公告）日：2003-09-18

  The subject invention pertains to electrochromic polymers and polymer electrochromic devices. In a specific embodiment, two complementary polymers can be matched and incorporated into dual polymer electrochromic devices. The anodically coloring polymers in accordance with the subject invention can allow control over the color, brightness, and environmental stability of an electrochromic window. In addition, high device contrast ratios, high transmittance changes, and high luminance changes can be achieved, along with half-second switching times for full color change. Also provided are electrochromic devices such as advertising signage, video monitors, stadium scoreboards, computers, announcement boards, warning systems for cell phones, warning/information systems for automobiles, greeting cards, electrochromic windows, billboards, electronic books, and electrical wiring. The subject invention also provides for the use of complementary electrochromic polymers in the manufacture of electrochromic devices. In some embodiments, the devices of the invention can be prepared using metal vapor deposition or line patterning.

  本发明涉及电致变色聚合物和聚合物电致变色器件。在一个特定的实施例中，可以将两种互补的聚合物配对并纳入双聚合物电致变色器件中。根据本发明的阳极着色聚合物可以允许控制电致变色窗户的颜色、亮度和环境稳定性。此外，可以实现高对比度比、高透射率变化和高亮度变化，以及半秒钟的全彩色变换时间。还提供了电致变色器件，例如广告标志、视频监视器、体育场记分牌、计算机、公告牌、手机警告系统、汽车警告/信息系统、贺卡、电致变色窗户、广告牌、电子书和电气布线。本发明还提供了在制造电致变色器件时使用互补电致变色聚合物的方法。在一些实施例中，可以使用金属蒸汽沉积或线路图案制备本发明的器件。