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十八烷基二甲基叔胺 | 124-28-7

中文名称
十八烷基二甲基叔胺
中文别名
N,N-二甲基十八胺;二甲基十八胺;地孟汀;N,N-二甲基正十八胺;二甲十八胺;N,N-二甲基-1-十八胺;十八叔胺;DMA1895
英文名称
N,N-dimethyl-n-octadecylamine
英文别名
octadecyldimethylamine;Dymanthine;N,N-dimethyloctadecan-1-amine
十八烷基二甲基叔胺化学式
CAS
124-28-7
化学式
C20H43N
mdl
MFCD00048496
分子量
297.568
InChiKey
NAPSCFZYZVSQHF-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:
    23 °C
  • 沸点:
    347 °C
  • 密度:
    0.8
  • 闪点:
    155 °C
  • 溶解度:
    氯仿(微溶)、己烷(微溶)
  • LogP:
    1.3-5.1 at 20℃ and pH7.1-8.8
  • 表面张力:
    32.2mN/m at 1g/L and 25℃
  • 解离常数:
    9.78 at 25℃
  • 物理描述:
    N,n-dimethyl-1-octadecanamine appears as a clear yellow liquid with a fishlike odor. Insoluble in water and less dense than water. Hence floats on water. Contact may irritate skin, eyes and mucous membranes. May be toxic by ingestion, inhalation or skin absorption. Used to make other chemicals.
  • 保留指数:
    2096
  • 稳定性/保质期:
    1. 基本性质:可与环氧乙烷硫酸二甲酯硫酸二乙酯氯甲烷苄等反应,生成不同的季盐阳离子。

    2. 本品低毒。

计算性质

  • 辛醇/水分配系数(LogP):
    9.1
  • 重原子数:
    21
  • 可旋转键数:
    17
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    3.2
  • 氢给体数:
    0
  • 氢受体数:
    1

ADMET

毒理性
  • 副作用
Dermatotoxin - 皮肤烧伤。
Dermatotoxin - Skin burns.
来源:Haz-Map, Information on Hazardous Chemicals and Occupational Diseases

安全信息

  • 危险等级:
    8
  • 危险品标志:
    C
  • 安全说明:
    S26,S36/37/39,S45
  • 危险类别码:
    R22,R34
  • 海关编码:
    2921199090
  • 危险品运输编号:
    2735
  • RTECS号:
    RG4200000
  • 包装等级:
    III
  • 危险类别:
    8
  • 危险性防范说明:
    P233,P260,P261,P264,P271,P273,P280,P301+P330+P331,P303+P361+P353,P304,P304+P340,P305+P351+P338,P310,P312,P321,P340,P363,P391,P403,P403+P233,P405,P501
  • 危险性描述:
    H314,H336,H400,H410
  • 储存条件:
    塑料桶包装,每桶重50千克。应贮存于阴凉、通风的地方,并远离火种和热源。 在长途运输时,外用木条箱保护,并在桶底衬垫稻草以增加安全性。

SDS

SDS:0b6c1e769f6a5faeb813397a514f53ba
查看
Name: N N-Dimethyloctadecylamine (Techn) 89% (GC) Material Safety Data Sheet
Synonym: Dimethylstearamine; Dymanthine
CAS: 124-28-7
Section 1 - Chemical Product MSDS Name:N N-Dimethyloctadecylamine (Techn) 89% (GC) Material Safety Data Sheet
Synonym:Dimethylstearamine; Dymanthine

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
124-28-7 N,N-Dimethyloctadecylamine 89 204-694-8
Hazard Symbols: C
Risk Phrases: 10 34

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Flammable. Causes burns.Corrosive.
Potential Health Effects
Eye:
Causes eye burns. May cause chemical conjunctivitis and corneal damage.
Skin:
Causes skin burns. May cause cyanosis of the extremities. May cause skin rash (in milder cases), and cold and clammy skin with cyanosis or pale color.
Ingestion:
May cause severe and permanent damage to the digestive tract. May cause gastrointestinal irritation with nausea, vomiting and diarrhea. Causes gastrointestinal tract burns. May cause perforation of the digestive tract. The toxicological properties of this substance have not been fully investigated. Ingestion of large amounts may cause CNS depression. May cause systemic effects.
Inhalation:
Causes chemical burns to the respiratory tract. The toxicological properties of this substance have not been fully investigated.
Aspiration may lead to pulmonary edema. Vapors may cause dizziness or suffocation. May cause systemic effects. May cause burning sensation in the chest.
Chronic:
Effects may be delayed.

Section 4 - FIRST AID MEASURES
Eyes: Get medical aid immediately. Do NOT allow victim to rub eyes or keep eyes closed. Extensive irrigation with water is required (at least 30 minutes).
Skin:
Get medical aid immediately. Immediately flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes. Wash clothing before reuse. Destroy contaminated shoes.
Ingestion:
Do not induce vomiting. If victim is conscious and alert, give 2-4 cupfuls of milk or water. Get medical aid immediately.
Inhalation:
Get medical aid immediately. Remove from exposure and move to fresh air immediately. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Do NOT use mouth-to-mouth resuscitation. If breathing has ceased apply artificial respiration using oxygen and a suitable mechanical device such as a bag and a mask.
Notes to Physician:

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. 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:
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. Discard contaminated shoes. 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# 124-28-7: 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: amine-like
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: 23 deg C
Autoignition Temperature: Not available.
Flash Point: 44 deg C ( 111.20 deg F)
Explosion Limits, lower: Not available.
Explosion Limits, upper: Not available.
Decomposition Temperature:
Solubility in water:
Specific Gravity/Density: .8000g/cm3
Molecular Formula: C20H43N
Molecular Weight: 297.57

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Stable under normal temperatures and pressures.
Conditions to Avoid:
Incompatible materials, ignition sources, excess heat, strong oxidants.
Incompatibilities with Other Materials:
Oxidizing agents.
Hazardous Decomposition Products:
Carbon monoxide, oxides of nitrogen, irritating and toxic fumes and gases, carbon dioxide.
Hazardous Polymerization: Has not been reported

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 124-28-7: RG4200000 LD50/LC50:
CAS# 124-28-7: Draize test, rabbit, eye: 20 mg/24H Moderate; Draize test, rabbit, skin: 20 mg/24H Moderate.
Carcinogenicity:
N,N-Dimethyloctadecylamine - 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: Amines, liquid, corrosive, n.o.s.*
Hazard Class: 8 (3)
UN Number: 2735
Packing Group: III
IMO
Shipping Name: Amines, liquid, corrosive, n.o.s.
Hazard Class: 8 (3)
UN Number: 2735
Packing Group: III
RID/ADR
Shipping Name: CORROSIVE LIQUID, FLAMMABLE, N.O.S.
Hazard Class: 8
UN Number: 2920
Packing group: II

Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: C
Risk Phrases:
R 10 Flammable.
R 34 Causes burns.
Safety Phrases:
S 9 Keep container in a well-ventilated place.
S 16 Keep away from sources of ignition - No
smoking.
S 25 Avoid contact with eyes.
S 28A After contact with skin, wash immediately with
plenty of water.
S 33 Take precautionary measures against static
discharges.
S 36/37/39 Wear suitable protective clothing, gloves
and eye/face protection.
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# 124-28-7: 2
Canada
CAS# 124-28-7 is listed on Canada's DSL List.
CAS# 124-28-7 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 124-28-7 is listed on the TSCA inventory.


SECTION 16 - ADDITIONAL INFORMATION
N/A

制备方法与用途

化学性质

这是一种浅棕色粘稠液体,在20℃时则为浅草黄色软质固体。它易溶于醇类溶剂,而不溶于

用途

该物质是季铵盐型阳离子表面活性剂的重要有机合成中间体,可用于生成不同的季盐阳离子。这些反应可以与环氧乙烷硫酸二甲酯硫酸二乙酯氯甲烷苄进行。由此获得的产物可应用于织物柔软、抗静电剂以及改善头发梳理性等产品中。此外,它还可用以生产驱虫剂。N,N-二甲基十八胺经过与环氧乙烷硝酸反应后,可以制得十八烷基二甲基羟乙基季硝酸盐(即抗静电剂SN)。

用途

该物质还可用于制备季盐、甜菜碱及氧化叔胺等化合物。

生产方法

N,N-二甲基十八胺可通过将十八胺甲醛甲酸缩合获得。具体步骤是首先在乙醇介质中搅拌均匀十八胺,随后在50-60℃下加入甲酸,搅拌数分钟后,在60-65℃下加入甲醛,升温至80-83℃并回流保温2小时后用液碱中和至pH值大于10,静置分层去后再进行减压蒸馏去除乙醇。冷却后即可得到N,N-二甲基十八胺

原料消耗定额如下:每吨产品需要工业品十八胺917千克、95%乙醇417千克、甲酸510千克和37%甲醛546千克。此外,还有直接由高级醇与二甲胺合成的方法。该方法是在存在催化剂的情况下,在180-220℃的液相条件下将十八醇二甲胺进行催化胺化反应,并脱除一分子后得到粗叔胺,再通过减压蒸馏获得高纯度N,N-二甲基十八胺。每吨产品需要消耗十八醇971千克和二甲胺170千克。

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:
    十八烷基二甲基叔胺双氧水 作用下, 以 乙醇 为溶剂, 反应 6.0h, 生成 N,N-二甲基十八烷基-N-氧化胺
    参考文献:
    名称:
    新型的低粘度,绿色和两亲性N-氧化物/苯乙酸基深共熔溶剂
    摘要:
    通过将苯乙酸(一种存在于蜂蜜中的天然分子)与胺N-氧化物(自然界中易于生物降解的分子)混合,制得了四种新型的深共晶溶剂(DES)。这些N-氧化物中的三个是两亲的。新型DES的凝固点非常低(从-34°C到20°C),并且粘度非常低,远低于迄今为止文献中最常用和使用的DES(氯化胆碱/尿素混合物)。电导率值较低,离子性分析表明这些DES为“超离子性”。它们的极性足够高,可以与其他常用溶剂或离子液体相比。
    DOI:
    10.1016/j.molliq.2017.05.084
  • 作为产物:
    描述:
    N n-二甲基-9-十八酰胺 在 sponge copper catalyst: 73.4percent Cu, 0.5percent Mg, 5.7percent Fe, 0.9percent Al 氢气 作用下, 以 为溶剂, 250.0 ℃ 、1.5 MPa 条件下, 以81.7%的产率得到十八烷基二甲基叔胺
    参考文献:
    名称:
    PROCESS FOR PRODUCING NITROGEN-CONTAINING COMPOUNDS
    摘要:
    本发明涉及一种在存在含有海绵铜催化剂的催化剂的情况下,通过还原酰胺化合物来生产三级胺的方法,所述海绵铜催化剂是通过浸出含有铜和铝的合金颗粒并干燥浸出的合金颗粒获得的。本发明提供了一种在无溶剂适度条件下将脂肪酸酰胺经过加氢还原处理以高产率产生含有少量副产物的高纯度脂肪族三级胺的方法。
    公开号:
    US20100179349A1
  • 作为试剂:
    描述:
    果糖二丙酮十八烷基二甲基叔胺磺酰胺 作用下, 以 邻二甲苯 为溶剂, 反应 0.5h, 生成 托吡酯
    参考文献:
    名称:
    [EN] PROCESS FOR THE PREPARATION OF ANTICONVULSANT DERIVATIVES OF TOPIRAMATE
    [FR] PROCEDE DE PREPARATION DE DERIVES DE TOPIRAMATE ANTICONVULSIFS
    摘要:
    本发明涉及一种制备一步法的果糖吡喃磺酰胺衍生物的方法,其通式为(I),其中X、R1、R3、R4、R5和R6如规范中所述。
    公开号:
    WO2004078769A1
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文献信息

  • USE OF NITROGEN COMPOUNDS QUATERNISED WITH ALKYLENE OXIDE AND HYDROCARBYL-SUBSTITUTED POLYCARBOXYLIC ACID AS ADDITIVES IN FUELS AND LUBRICANTS
    申请人:BASF SE
    公开号:US20160130514A1
    公开(公告)日:2016-05-12
    The invention relates to the use of quaternized nitrogen compounds as a fuel and lubricant additive or kerosene additive, such as in particular as a detergent additive, for decreasing or preventing deposits in the injection systems of direct-injection diesel engines, in particular in common rail injection systems, for decreasing the fuel consumption of direct-injection diesel engines, in particular of diesel engines having common rail injection systems, and for minimizing the power loss in direct-injection diesel engines, in particular in diesel engines having common rail injection systems; the invention further relates to the use as an additive for petrol, in particular for operation of DISI engines.
    该发明涉及将季化氮化合物用作燃料和润滑剂添加剂或煤油添加剂,特别是作为清洁剂添加剂,用于减少或预防直喷柴油发动机的喷射系统中的沉积物,在特定是在共轨喷射系统中,用于降低直喷柴油发动机的燃料消耗,特别是具有共轨喷射系统的柴油发动机,并用于减少直喷柴油发动机的功率损失,特别是在具有共轨喷射系统的柴油发动机中;该发明还涉及将其用作汽油添加剂,特别是用于DISI发动机的运行。
  • Synthesis of 4-ketocyclopentene and cyclopentadiene compounds
    申请人:——
    公开号:US20020002308A1
    公开(公告)日:2002-01-03
    A process for forming 4-ketocyclopentene and substituted 4-ketocyclopentene compounds starting from the corresponding 1-carbohydrocarbyloxy-2-keto-4-hydroxy-5-cyclopentene by reduction followed by decarboxylation using zinc dichloride or zinc dibromide. The ketone may thereafter be converted to a cyclopentadiene compound by reducing the ketone to form an alcohol, replacing the hydroxyl functionality of the alcohol under substitution conditions with a leaving group, and deprotonating the resulting product under base induced elimination conditions to form the cyclopentadiene compound. Alternatively functionalized cyclopentadienyl compounds can be produced without isolation of an unsubstituted cyclopentadienyl compound by combining the elimination and deprotonation steps with a replacement step in a single unit operation.
    从相应的1-碳氢烷氧基-2-酮-4-羟基-5-环戊烯开始,通过还原后脱羧,使用氯化锌溴化锌形成4-酮环戊烯和取代的4-酮环戊烯化合物的过程。然后,可以通过将酮还原形成醇,用取代条件下的离去基取代醇的羟基官能团,并在碱诱导的消除条件下去质子化所得产物以形成环戊二烯化合物。或者,可以通过将消除和去质子化步骤与替换步骤结合在单个单元操作中,而无需分离未取代的环戊二烯基化合物来生产功能化的环戊二烯基化合物。
  • Antimicrobial Activity of Gemini Surfactants with Ether Group in the Spacer Part
    作者:Bogumil Eugene Brycki、Adrianna Szulc、Iwona Kowalczyk、Anna Koziróg、Ewelina Sobolewska
    DOI:10.3390/molecules26195759
    日期:——

    Due to their large possibility of the structure modification, alkylammonium gemini surfactants are a rapidly growing class of compounds. They exhibit significant surface, aggregation and antimicrobial properties. Due to the fact that, in order to achieve the desired utility effect, the minimal concentration of compounds are used, they are in line with the principle of greenolution (green evolution) in chemistry. In this study, we present innovative synthesis of the homologous series of gemini surfactants modified at the spacer by the ether group, i.e., 3-oxa-1,5-pentane-bis(N-alkyl-N,N-dimethylammonium bromides). The critical micelle concentrations were determined. The minimal inhibitory concentrations of the synthesized compounds were determined against bacteria Escherichia coli ATCC 10536 and Staphylococcus aureus ATCC 6538; yeast Candida albicans ATCC 10231; and molds Aspergillus niger ATCC 16401 and Penicillium chrysogenum ATCC 60739. We also investigated the relationship between antimicrobial activity and alkyl chain length or the nature of the spacer. The obtained results indicate that the synthesized compounds are effective microbicides with a broad spectrum of biocidal activity.

    由于烷基双链表面活性剂具有结构修改的大可能性,它们是一类快速增长的化合物。它们表现出显著的表面、聚集和抗微生物特性。由于为了实现所需的效果,使用了化合物的最小浓度,它们符合化学中的绿色演化原则。在这项研究中,我们提出了一种创新的合成方法,合成了通过醚基修饰的同系列双链表面活性剂,即3-氧杂-1,5-戊烷-双(N-烷基-N,N-二甲基化物)。确定了临界胶束浓度。确定了合成化合物对大肠杆菌ATCC 10536和黄色葡萄球菌ATCC 6538;酵母白念珠菌ATCC 10231;以及曼氏黑曲霉ATCC 16401和青霉菌ATCC 60739的最小抑菌浓度。我们还研究了抗微生物活性与烷基链长度或间隔物性质之间的关系。得到的结果表明,合成的化合物是具有广谱生物杀灭活性的有效微生物杀菌剂。
  • Effect of the alkyl chain length on micelle formation for bis(N-alkyl-N,N-dimethylethylammonium)ether dibromides
    作者:Bogumil Brycki、Adrianna Szulc、Hanna Koenig、Iwona Kowalczyk、Tomasz Pospieszny、Sara Górka
    DOI:10.1016/j.crci.2019.04.002
    日期:2019.5
    Résumé Dimeric alkylammonium salts – gemini surfactants – due to their unusual very low critical micelle concentration and minimal inhibitory concentration are subject to intensive research as surface active and antimicrobial compounds. Thanks to the presence of two positively charged nitrogen atoms and a large molecular surface, gemini surfactants are also very efficient corrosion inhibitors. To strengthen the electrostatic adsorption of ammonium cations on a metal surface, which is a key parameter in the inhibition of corrosion, heteroatoms (O, S, N, or P) and π-electron systems can be introduced into the gemini surfactant structure to increase chemical adsorption. In this study, we investigated the relationship between the alkyl chain length and critical micelle concentration for gemini surfactants containing an oxygen atom in the spacer, that is, bis(N-alkyl-N,N-dimethylethylammonium)ether dibromides, for potential use as corrosion inhibitors.
    简历 二聚烷基盐——双子表面活性剂——因其异常低的临界胶束浓度和最小抑制浓度,作为表面活性和抗菌化合物受到了深入研究。由于含有两个正电荷的氮原子和大分子表面,双子表面活性剂也是非常高效的腐蚀抑制剂。为了增强阳离子在属表面的静电吸附——这是抑制腐蚀的关键参数——可以在双子表面活性剂结构中引入杂原子(O、S、N或P)和π电子体系以增加化学吸附。在本研究中,我们探究了含有氧原子间隔基的双子表面活性剂,即双(N-烷基-N,N-二甲基乙基)醚二化物,作为潜在腐蚀抑制剂时,烷基链长度与临界胶束浓度之间的关系。
  • CONTACT-KILLING, QAC FUNCTIONALIZED THERMOPLASTIC POLYURETHANE FOR CATHETER APPLICATIONS
    申请人:THE UNIVERSITY OF AKRON
    公开号:US20190106525A1
    公开(公告)日:2019-04-11
    In various embodiments, the present invention provides a functionalized thermoplastic polyurethane (TPU) containing bulk incorporated or surface-grafted quaternary ammonium compounds (QAC)s for contact-killing of a variety of microbes, where the QACs are on the surface of TPU to provide a sterile surface material that prevents bacteria commonly involved in device-associated infections (DAIs) from proliferating. The functionalized TPUs of the present invention can be formed into a wide variety of 3-dimensional shapes, such as catheters, medical tubing, laryngeal or tracheal stents, sutures, prosthetics, wound dressings, and/or a coating for medical devices and contains the residue of either a QAC containing diol monomer or an alkene functional diol monomer, which then allows the TPU to be functionalized with a QAC containing disulfide or free thiol compound, to form a quaternary ammonium functionalized thermoplastic polyurethane compound having antimicrobial properties for use in medical devices.
    在各种实施方式中,本发明提供了一种功能化的热塑性聚酯(TPU),其中包含大量引入或表面接枝的季化合物(QAC),用于接触杀灭多种微生物,其中QAC位于TPU表面,以提供一种无菌表面材料,防止通常涉及设备相关感染(DAIs)的细菌繁殖。本发明的功能化TPU可以形成多种三维形状,例如导管、医疗管、喉部或气管支架、缝合线、假体、伤口敷料和/或医疗设备的涂层,并包含含有二醇单体或烯功能二醇单体的QAC残留物,这使得TPU可以用含有二键或自由巯基化合物的QAC进行功能化,以形成具有用于医疗设备的抗菌性能的季功能化热塑性聚酯化合物。
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
hnmr
mass
cnmr
ir
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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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