摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1,1-二氟乙烷 | 75-37-6

中文名称
1,1-二氟乙烷
中文别名
氢氟碳152A;偏二氟乙烷;氟里昂-152;1,1-二氟乙烷;氟里昂-152a
英文名称
1,1-difluoroethane
英文别名
HFC-152a
1,1-二氟乙烷化学式
CAS
75-37-6;25497-28-3
化学式
C2H4F2
mdl
MFCD00000449
分子量
66.0506
InChiKey
NPNPZTNLOVBDOC-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

  • 物理描述:
    1,1-Difluoroethane is colorless, odorless gas shipped as a liquefied gas under its vapor pressure. Contact with the liquid can cause frostbite. It is easily ignited. Its vapors are heavier than air and a flame can travel back to the source of leak very easily. This leak can be either a liquid or vapor leak. It can asphyxiate by the displacement of air. Under prolonged exposure to fire or heat the containers may rupture violently and rocket.
  • 颜色/状态:
    Colorless gas
  • 气味:
    Odorless
  • 沸点:
    -24.9 °C
  • 熔点:
    -117.0 °C
  • 闪点:
    < -50 °C (open cup)
  • 溶解度:
    In water, 3.2X10+3 mg/L at 25 °C
  • 密度:
    0.896 c/cu cm at 25 °C, >1 atm
  • 蒸汽密度:
    2.3 (Air = 1)
  • 蒸汽压力:
    4,550 mm Hg at 25 °C
  • 亨利常数:
    0.02 atm-m3/mole
  • 大气OH速率常数:
    3.40e-14 cm3/molecule*sec
  • 稳定性/保质期:
    Stable under recommended storage conditions.
  • 自燃温度:
    455 °C
  • 粘度:
    0.263 cP at 50 °F
  • 燃烧热:
    -7,950 Btu/lb = -4,420 cal/g = -185X10+5 J/kg
  • 汽化热:
    19.08 kJ/mol ar 25 °C
  • 表面张力:
    11.25 dynes/cm = 0.01125 N/m at 20 °C (liquid)
  • 保留指数:
    326;242

计算性质

  • 辛醇/水分配系数(LogP):
    1.4
  • 重原子数:
    4
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    2

ADMET

毒理性
  • 毒性总结
识别和使用:1,1-二氟乙烷(HFC-152a)是一种无色、无味的气体。HFC-152a的主要用途是作为气溶胶推进剂和泡沫膨胀剂。其他潜在用途包括制冷混合物和催化剂再生。是制备乙烯氟化物的中间体。人类暴露和毒性:几名志愿者暴露于500,000 ppm的HFC 152a几分钟后,报告出现了镇痛和即将失去意识的情况。液体的快速蒸发可能导致冻伤。该物质可能对心血管系统产生影响,导致心脏疾病。氟化烃的滥用正在上升,特别是在青少年人群中。吸入由HFC-152a组成的气溶胶电脑清洁喷雾导致了明显的上下唇面部肿胀,与血管性水肿相符。患者还出现了QT间期延长、轻度吸气性喉鸣,但没有荨麻疹。在另一个案例中,连续两天几乎不间断地吸食后,出现了急性心肌损伤、全心力减弱、横纹肌溶解、急性肾损伤和暴发性肝炎。卤代烃吸入滥用的一种严重但很少报告的并发症是严重的粘膜冻伤。在体外人类淋巴细胞染色体畸变试验中,HFC-152a显示出微弱的致裂变性。 动物研究:HFC-152a具有较低的急性吸入毒性。重复剂量研究表明有一定的刺激性。HFC-152a可能在狗同时接触高浓度暴露和高剂量外源性肾上腺素时产生心脏过敏。在为期2周的重复剂量吸入研究中,大鼠在100,000 ppm的暴露水平下,HFC-152a显示出麻醉性质。在大鼠吸入25,000 ppm HFC-152a三个月的暴露后,没有观察到不良反应。在一项发育研究中,雌性大鼠在怀孕的第6天至第15天,每天6小时,通过吸入暴露至50,000 ppm。在任何测试的浓度下都没有观察到与化合物相关的母体和发育影响。在雄性和雌性大鼠每天6小时,每周5天,暴露于25,000 ppm HFC-152a 3、12或24个月的实验中,没有观察到生殖器官的的组织病理学或重量影响。在一项为期2年的生物鉴定中,HFC-152a在大鼠吸入暴露水平高达25,000 ppm时,不具有致癌性。HFC-152a在Salmonella typhimurium和Escherichia coli菌株的体外细菌反向突变试验(Ames试验)中不具有致突变性。在大鼠体内微粒体试验中,通过全身吸入给药,没有显示出染色体损伤或骨髓细胞毒性的证据。
IDENTIFICATION AND USE: 1,1-Difluoroethane (HFC-152a) is a colorless, odorless gas. The primary uses for HFC-152a are as an aerosol propellant and a foam expansion agent. Other potential uses include refrigeration blends and catalyst regeneration. Intermediate to vinyl fluoride. HUMAN EXPOSURE AND TOXICITY: Several volunteers were exposed to 500,000 ppm of HFC 152a for several min. Analgesia and an impending loss of consciousness were reported. Rapid evaporation of the liquid may cause frostbite. The substance may cause effects on the cardiovascular system , resulting in cardiac disorders. Abuse of fluorinated hydrocarbons is on the rise, especially among the adolescent population. Inhaling aerosolized computer-cleaning spray composed of HFC-152a led to marked upper and lower lip facial swelling consistent with angioedema. The patient also had a prolonged QT interval, mild inspiratory stridor, but no urticaria. In other case, acute myocardial injury and global hypokinesis along with rhabdomyolysis, acute kidney injury, and fulminant hepatitis developed after 2 days of nearly continuous huffing. A serious but rarely reported complication of halogenated hydrocarbon inhalation abuse is severe mucosal frostbite. HFC-152a showed evidence of weak clastogenicity in an in vitro human lymphocyte chromosome aberration test. ANIMAL STUDIES: HFC-152a has low acute inhalation toxicity. The repeat dose studies show some potential for irritation. HFC-152a has the potential to produce cardiac sensitization in dogs challenged simultaneously with high exposure concentrations and high doses of exogenous epinephrine. HFC-152a had anesthetic properties at a 100,000 ppm exposure level during a 2-week repeated dose inhalation study in rats. No adverse effects were observed in rats following a 3-month inhalation exposure to 25,000 ppm HFC-152a. In a developmental study, female rats were exposed via inhalation up to 50,000 ppm during days 6 to 15 of pregnancy for 6 hours per day. No compound related maternal and developmental effects were observed at any of the concentrations tested. No histopathological or weight effects on reproductive organs were observed in male and female rats exposed up to 25,000 ppm HFC-152a for 6 hours per day, 5 days per week for 3, 12 or 24 months. . In a 2-year bioassay, HFC-152a was not carcinogenic to rats at inhalation exposure levels up to 25,000 ppm. HFC-152a was not mutagenic in the in vitro bacterial reverse mutation test (Ames test) in Salmonella typhimurium and Escherichia coli strains. An in vivo rat Micronucleus Test did not show any evidence of chromosome damage or bone marrow cell toxicity when administered by whole body inhalation.
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 暴露途径
该物质可以通过吸入被身体吸收。
The substance can be absorbed into the body by inhalation.
来源:ILO-WHO International Chemical Safety Cards (ICSCs)
毒理性
  • 吸入症状
晕眩。嗜睡。昏迷。窒息。
Dizziness. Drowsiness. Unconsciousness. Suffocation.
来源:ILO-WHO International Chemical Safety Cards (ICSCs)
毒理性
  • 皮肤症状
接触液体时:冻伤。
ON CONTACT WITH LIQUID: FROSTBITE.
来源:ILO-WHO International Chemical Safety Cards (ICSCs)
毒理性
  • 眼睛症状
看皮肤。
See Skin.
来源:ILO-WHO International Chemical Safety Cards (ICSCs)
吸收、分配和排泄
1,1-二氟乙烷(DFE)是一种卤代烃,用作清洁电子设备和喷枪绘画产品的推进剂。滥用时,吸入DFE会导致中毒和肌肉协调能力丧失。为了研究DFE的毒代动力学,将三组(每组n=3)Sprague-Dawley大鼠暴露于20升/分钟的DFE,持续30秒。实验模型旨在模仿滥用时的暴露情况,这一方案尚未进行过。在0、10、20、30、45、60、120、240、480和900秒时收集组织(血液、大脑、心脏、肝脏和肾脏)。平均峰值DFE水平为血液352毫克/升或毫克/千克,大脑519毫克/升或毫克/千克,心脏338毫克/升或毫克/千克,肝脏187毫克/升或毫克/千克,肾脏364毫克/升或毫克/千克。给药剂量的总吸收百分比为4.0%。各个部位的吸收百分比为血液2.72%,大脑0.38%,心脏0.15%,肝脏0.41%,肾脏0.32%。所有动物在20秒内表现出中毒迹象,表现为精神萎靡、俯卧和失去翻正反射。明显的中毒状态持续了大约4分钟,此时血液中DFE平均为21毫克/升,大脑中为17毫克/千克。在4到8分钟之间,动物在处理过程中继续表现出镇静迹象,表现为攻击性和兴奋性降低。8分钟后没有明显的中毒迹象,血液和大脑中的水平分别降至10和6毫克/升或千克。浓度(对数)与时间的图表符合双室模型。初始分布迅速,平均半衰期(t(1/2))在α相为血液9秒,大脑18秒,心脏组织27秒。在β斜率消除期间,平均t(1/2)为血液86秒,大脑110秒,心脏168秒。晚期消除半衰期较长,血液γ=240秒,大脑γ=340秒,心脏γ=231秒。急性暴露后,Vd=0.06升,β=0.48分钟(-1),AUC=409.8毫克·分钟/升,血液清除率(CL)为0.03升/分钟。计算出的毒代动力学数据可能低估了这些参数,如果DFE长期滥用,由于重复给药,DFE会继续进入低灌注组织。
1,1-Difluoroethane (DFE) is a halogenated hydrocarbon used as a propellant in products designed for dusting electronic equipment and air brush painting. When abused, inhaled DFE produces intoxication and loss of muscular coordination. To investigate DFE toxicokinetics, groups (n = 3) of Sprague-Dawley rats were exposed to 30 s of 20 L/min DFE. The experimental model was designed to mimic exposure during abuse, a protocol which has not been conducted. Tissue collection (blood, brain, heart, liver, and kidney) occurred at 0, 10, 20, 30, 45, 60, 120, 240, 480, and 900 s. Average peak DFE levels were blood 352, brain 519, heart 338, liver 187, and kidney 364 mg/L or mg/kg. The total percent uptake of the administered dose was 4.0%. Uptake into individual compartments was 2.72, 0.38, 0.15, 0.41, and 0.32% for blood, brain, heart, liver, and kidney, respectively. All animals showed signs of intoxication within 20 s manifested as lethargy, prostration and loss of righting reflex. Marked intoxication continued for about 4 min when DFE averaged 21 mg/L in blood and 17 mg/kg in brain. Between 4 and 8 min, animals continued to show signs of sedation as evidenced by reduced aggression and excitement during handling. No discernable intoxication was evident after 8 min and blood and brain levels had fallen to 10 and 6 mg/L or kg, respectively. Plots of concentration (log) versus time were consistent with a two compartment model. Initial distribution was rapid with average half life (t((1/2))) during the alpha phase of 9 s for blood, 18 s for brain and 27 s in cardiac tissue. During beta slope elimination average t((1/2)) was 86 s in blood, 110 s in brain and 168 s in heart. Late elimination half lives were longer with blood gamma = 240 s, brain gamma = 340 s, and heart gamma = 231 s. Following acute exposure the Vd = 0.06 L, beta = 0.48 min(-1), AUC = 409.8 mg.min L(-1), and CL from blood was 0.03 L min(-1). The calculated toxicokinetic data may underestimate these parameters if DFE is abused chronically due to continued uptake into lowly perfused tissues with repeated dosing.
来源:Hazardous Substances Data Bank (HSDB)
吸收、分配和排泄
这项研究旨在确定人体吸入1,1-二氟乙烷(HFC-152a)的毒物动力学。健康志愿者在暴露室中以轻度运动暴露于0、200或1000 ppm的1,1-二氟乙烷2小时。在暴露后长达22小时的时间内采集毛细血管血、尿液和呼出的空气,并分析其中的1,1-二氟乙烷。尿液中分析了氟化物和其他潜在代谢物。评估了刺激症状和中枢神经系统影响的症状,并在血液中分析了炎症标志物。在暴露于200和1000 ppm的几分钟内,1,1-二氟乙烷在血液中迅速增加,分别达到平均浓度7.4和34.3微摩尔。暴露后血液中的下降是快速的,与呼出气体的下降平行。血液和呼吸的时间过程与PBPK模型获得的结果一致。PBPK模拟表明,在1000 ppm暴露期间,净吸收为6.6毫摩尔(6.7%),这与暴露后呼出的量相对应。暴露于1000 ppm后,尿液中排泄了大约20微摩尔的过量氟化物(按摩尔计算吸入的1,1-二氟乙烷的0.013%),与对照组相比。尿液中未检测到含氟代谢物。症状评分和炎症标志物的变化未显示与暴露相关的效果。
The aim of this study was to determine the toxicokinetics of inhaled 1,1-difluoroethane (HFC-152a) in humans. Healthy volunteers were exposed to 0, 200 or 1000 ppm 1,1-difluoroethane for 2 hr at light exercise in an exposure chamber. Capillary blood, urine and exhaled air were sampled up to 22 hr post-exposure and analyzed for 1,1-difluoroethane. Fluoride and other potential metabolites were analyzed in urine. Symptoms of irritation and central nervous system effects were rated and inflammatory markers were analyzed in blood. Within a few minutes of exposure to 200 and 1000 ppm, 1,1-difluoroethane increased rapidly in blood and reached average levels of 7.4 and 34.3 uM, respectively. The post-exposure decreases in blood were fast and parallel to those in exhaled air. The observed time courses in blood and breath agreed well with those obtained with the PBPK model. The PBPK simulations indicate a net uptake during exposure to 1000 ppm of 6.6 mmol (6.7%) which corresponds to the amount exhaled post-exposure. About 20 umol excess fluoride (0.013% of inhaled 1,1-difluoroethane on a molar basis) was excreted in urine after exposure to 1000 ppm, compared to control. No fluorine-containing metabolites were detected in urine. Symptom ratings and changes in inflammatory markers revealed no exposure-related effects.
来源:Hazardous Substances Data Bank (HSDB)

安全信息

  • 危险品标志:
    F
  • 安全说明:
    S16,S33,S36,S38
  • 危险类别码:
    R11
  • WGK Germany:
    1
  • RTECS号:
    KI1410000
  • 海关编码:
    2903399090
  • 危险类别:
    2.1
  • 危险标志:
    GHS02,GHS04
  • 危险品运输编号:
    UN 1030 2.1
  • 危险性描述:
    H220,H280
  • 危险性防范说明:
    P210,P377,P381,P410 + P403

SDS

SDS:effe0f09dd4820bef6bc7d65fb200b18
查看

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:
    1,1-二氟乙烷 作用下, 生成 二氯二氟甲烷
    参考文献:
    名称:
    Production of dichlorodifluoromethane
    摘要:
    公开号:
    US02417059A1
  • 作为产物:
    描述:
    1,1-二氯乙烷chromium(III) oxide 氢氟酸 作用下, 200.0 ℃ 、200.0 kPa 条件下, 反应 100.0h, 以62%的产率得到1,1-二氟乙烷
    参考文献:
    名称:
    [EN] METHOD FOR PURIFICATION OF 1,1-DICHLOROETHANE AND PROCESS FOR PRODUCTION OF 1,1-DIFLUOROETHANE USING THIS METHOD
    [FR] PROCÉDÉ DE PURIFICATION DU 1,1-DICHLOROÉTHANE ET PROCESSUS DE PRODUCTION DU 1,1-DIFLUOROÉTHANE EN UTILISANT CE PROCÉDÉ
    摘要:
    将含有硝基和/或羟基化合物作为稳定剂的1,1-二氯乙烷与平均孔径为3.4至11A的沸石和/或平均孔径为3.4至11A的碳质吸附剂在液相中接触。通过简单方便的方法有效地去除1,1-二氯乙烷中的稳定剂,并可以经济地生产1,1-二氟乙烷。
    公开号:
    WO2005102970A1
  • 作为试剂:
    描述:
    4-二甲氨基吡啶 、 [(MesNacnac)MgMg(MesNacnac)] 在 1,1-二氟乙烷 作用下, 以 氘代苯 为溶剂, 60.0 ℃ 、100.0 kPa 条件下, 生成
    参考文献:
    名称:
    镁试剂对 HFC 的脱氟
    摘要:
    一系列 HFC 与含有 Mg-Mg 键的主族试剂反应,导致脱氟,形成相应的氟化镁络合物。对于 1,1,1,2-四氟乙烷 (HFC-134a),氟化物的生成与 1,1-二氟乙烯的选择性形成同时发生。进行 DFT 计算是为了更好地了解选择性,并比较该系统中 sp 3 C-F 键活化与 sp 3 C-H 键活化的势垒。
    DOI:
    10.1039/d4dt00636d
点击查看最新优质反应信息

文献信息

  • Estimation of Atmospheric Lifetimes of Hydrofluorocarbons, Hydrofluoroethers, and Olefins by Chlorine Photolysis Using Gas-Phase NMR Spectroscopy
    作者:Alexander A. Marchione、Paul J. Fagan、Eric J. Till、Robert L. Waterland、Concetta LaMarca
    DOI:10.1021/ac800883t
    日期:2008.8.1
    hydrofluoroethers and relative rates of reaction with photolyzed chlorine in excess at ambient temperature. These kinetic systems were studied by nuclear magnetic resonance (NMR) spectroscopy in the gas phase, marking the first application of NMR spectroscopy to this field. The square of the Pearson coefficient R for the linear correlation between observed reaction rates and accepted atmospheric lifetimes was 0.87
    在一组氢氟烃和氢氟醚的公认大气寿命与在环境温度下与过量光解氯的相对反应速率之间存在经验相关性。在气相中通过核磁共振(NMR)光谱研究了这些动力学系统,这标志着NMR光谱在该领域的首次应用。对于观察到的反应速率与可接受的大气寿命之间的线性相关性,皮尔逊系数R的平方对于寿命小于20年的化合物为0.87。该方法扩展到乙烯和丙烯的研究。发现丙烯在23摄氏度下的反应速率是乙烯的1.25倍。
  • Nitroxide chemistry. Part XVII [1]. Reaction of bistrifluoromethyl nitroxide with some halogenoalkanes and related alkenes
    作者:R.E. Banks、J.A. Bernardin、R.N. Haszeldine、B. Justin、A. Vavayannis
    DOI:10.1016/s0022-1139(00)81779-0
    日期:1981.4
    CHXYZ, with bistrifluoromethyl nitroxide. The 1,2-bis(bistrifluoromethylamino-oxy)alkanes (CF3)2NOCH2CXYON(CF3)2 were obtained as by-products in the reactions involving the ethanes CH3CHXY (X = H, Y = F or Cl; X = Y = F); these products, like their analogues (CF3)2NOCHFCF2ON(CF3)2 and (CF3)2NOCH2CCl2ON(CF3)2, were also prepared via attack of bistrifluoromethyl nitroxide on the corresponding ethenes.
    单(双三氟甲基氨基氧基)烷烃(CF 3)2 NOCXYZ(X = Y = F,Z = Cl; X = H,Y = F或Cl,Z = CH 3 ; X = Y = F,Z = CH 3; X = H,Y = Cl或Br,Z = CF 3; X = Cl,Y = Br,Z = CF 3)是通过用双三氟甲基硝基氧处理适当的卤代烷烃CHXYZ而合成的。在涉及乙烷CH 3 CHXY(X = H,Y = F或Cl)的反应中作为副产物获得1,2-双(双三氟甲基氨基-氧基)烷烃(CF 3)2 NOR 2 CXYON(CF 3)2。 ; X = Y = F); 这些产品,如它们的类似物(CF 3)2 NOCHFCF 2 ON(CF 3)2和(CF 3)2 NOCH 2的CCl 2 ON(CF 3)2,也通过在对应的ethenes三氟甲基氮氧自由基的攻击制备。
  • FLP-Catalyzed Monoselective C–F Functionalization in Polyfluorocarbons at Geminal or Distal Sites
    作者:Richa Gupta、Dipendu Mandal、Amit K. Jaiswal、Rowan D. Young
    DOI:10.1021/acs.orglett.1c00346
    日期:2021.3.5
    positions. This methodology can be applied to aromatic-, ether-, thioether-, and alkyl-supported fluoromethyl groups. We expand the range of FLP base partners that work with monoselective C–F activation to include sulfide. The activated products can be subsequently functionalized via SN2 substitutions, photoredox-alkylations, and Suzuki couplings.
    我们报道了受挫的路易斯对(FLP)催化的一系列脂族多氟化碳具有同等的双链和双链CF位置的单选择性CF活化。该方法可以应用于芳族,醚,硫醚和烷基支持的氟甲基。我们扩大了与单选择性C–F激活一起使用的FLP基础合作伙伴的范围,以包括硫化物。随后可以通过S N 2取代,光氧化还原烷基化和Suzuki偶联将活化的产物官能化。
  • [EN] PROCESS FOR PURIFYING PENTAFLUOROETHANE, PROCESS FOR PRODUCING THE SAME, AND USE THEREOF<br/>[FR] PROCEDE DE PURIFICATION DE PENTAFLUOROETHANE, PROCEDE DE PRODUCTION DE PENTAFLUOROETHANE, ET UTILISATION DE CE PENTAFLUOROETHANE
    申请人:SHOWA DENKO KK
    公开号:WO2004005226A1
    公开(公告)日:2004-01-15
    ABSTRACT A process comprising bringing crude pentafluoroethane containing at least one compound selected from the group consisting of hydrofluorocarbons containing one carbon atom, hydrochlorofluorocarbons containing one carbon atom and hydrochlorocarbons containing one carbon atom, into contact with an adsorbent comprising a zeolite having an average pore size of 3 to 6 Å and a silica/aluminum ratio of 2.0 or less and/or a carbonaceous adsorbent having an average pore size of 3.5 to 6 Å, to reduce the content of the compound. The purified gas can be used as a low temperature refrigerant or an etching gas.
    摘要:一种过程包括将含有至少一种来自羟氟烃、含有一个碳原子的氢氟烃和含有一个碳原子的氯碳烃的混合氟乙烷原料与一种吸附剂接触,该吸附剂包括平均孔径为3至6 Å且硅铝比不超过2.0的沸石和/或平均孔径为3.5至6 Å的碳质吸附剂,以减少所述化合物的含量。纯化后的气体可用作低温制冷剂或蚀刻气体。
  • Efficient Synthesis of New Fluorinated Building Blocks by means of Hydroformylation
    作者:Lidia Fanfoni、Lisa Diab、Tomas Smejkal、Bernhard Breit
    DOI:10.2533/chimia.2014.371
    日期:——
    Hydroformylation of fluorinated alkenes is an efficient method for the preparation of fluorinated functionalized building blocks for the synthesis of biologically active target structures. In this article we summarize known hydroformylation reactions of fluorinated olefins and we add new results from our research groups. Particular attention is paid to the remarkable influence of organofluorine substituents
    氟化烯烃的加氢甲酰化是制备用于合成生物活性靶结构的氟化官能化结构单元的有效方法。在本文中,我们总结了氟化烯烃的已知加氢甲酰化反应,并增加了我们研究组的新结果。特别注意有机氟取代基对加氢甲酰化反应的催化剂活性,区域选择性和立体选择性的显着影响。
查看更多

表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
查看更多图谱数据,请前往“摩熵化学”平台
mass
查看更多图谱数据,请前往“摩熵化学”平台
ir
查看更多图谱数据,请前往“摩熵化学”平台
  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
查看更多图谱数据,请前往“摩熵化学”平台
Assign
Shift(ppm)
查看更多图谱数据,请前往“摩熵化学”平台
测试频率
样品用量
溶剂
溶剂用量
查看更多图谱数据,请前往“摩熵化学”平台