CN113336630B - 一种乙基香兰素共晶化合物及其制备方法和应用 - Google Patents
一种乙基香兰素共晶化合物及其制备方法和应用 Download PDFInfo
- Publication number
- CN113336630B CN113336630B CN202110538885.0A CN202110538885A CN113336630B CN 113336630 B CN113336630 B CN 113336630B CN 202110538885 A CN202110538885 A CN 202110538885A CN 113336630 B CN113336630 B CN 113336630B
- Authority
- CN
- China
- Prior art keywords
- ethyl vanillin
- eutectic compound
- eutectic
- compound
- ethyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- CBOQJANXLMLOSS-UHFFFAOYSA-N ethyl vanillin Chemical compound CCOC1=CC(C=O)=CC=C1O CBOQJANXLMLOSS-UHFFFAOYSA-N 0.000 title claims abstract description 172
- 229940073505 ethyl vanillin Drugs 0.000 title claims abstract description 86
- 230000005496 eutectics Effects 0.000 title claims abstract description 69
- 150000001875 compounds Chemical class 0.000 title claims abstract description 68
- 238000002360 preparation method Methods 0.000 title claims abstract description 9
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000004202 carbamide Substances 0.000 claims abstract description 20
- 235000019504 cigarettes Nutrition 0.000 claims abstract description 19
- 239000013078 crystal Substances 0.000 claims description 20
- 238000007789 sealing Methods 0.000 claims description 12
- 241000208125 Nicotiana Species 0.000 claims description 8
- 235000002637 Nicotiana tabacum Nutrition 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 239000002904 solvent Substances 0.000 claims description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical group CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 7
- 235000013355 food flavoring agent Nutrition 0.000 claims description 7
- 239000000796 flavoring agent Substances 0.000 claims description 6
- 239000000706 filtrate Substances 0.000 claims description 5
- 238000005303 weighing Methods 0.000 claims description 5
- 238000004090 dissolution Methods 0.000 claims description 4
- 238000001914 filtration Methods 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 230000000391 smoking effect Effects 0.000 abstract description 15
- 239000003205 fragrance Substances 0.000 abstract description 14
- 239000000178 monomer Substances 0.000 abstract description 10
- 235000013599 spices Nutrition 0.000 abstract description 10
- 230000014759 maintenance of location Effects 0.000 abstract description 2
- 238000002844 melting Methods 0.000 abstract description 2
- 230000008018 melting Effects 0.000 abstract description 2
- 238000011156 evaluation Methods 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000002441 X-ray diffraction Methods 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 description 2
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Natural products C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- 238000012512 characterization method Methods 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 238000012258 culturing Methods 0.000 description 2
- 239000003571 electronic cigarette Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 229960002715 nicotine Drugs 0.000 description 2
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 2
- 238000001144 powder X-ray diffraction data Methods 0.000 description 2
- -1 pyrazine compound Chemical class 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- 238000009210 therapy by ultrasound Methods 0.000 description 2
- WJUFSDZVCOTFON-UHFFFAOYSA-N veratraldehyde Chemical compound COC1=CC=C(C=O)C=C1OC WJUFSDZVCOTFON-UHFFFAOYSA-N 0.000 description 2
- JMKUTMOIKCXELD-UHFFFAOYSA-N (1-Methylethenyl)pyrazine Chemical compound CC(=C)C1=CN=CC=N1 JMKUTMOIKCXELD-UHFFFAOYSA-N 0.000 description 1
- DYZSLXGUSWETQL-UHFFFAOYSA-N 2-pyrazin-2-ylbutan-2-yl hydrogen carbonate Chemical compound CCC(C)(C1=NC=CN=C1)OC(=O)O DYZSLXGUSWETQL-UHFFFAOYSA-N 0.000 description 1
- 206010013911 Dysgeusia Diseases 0.000 description 1
- 235000009499 Vanilla fragrans Nutrition 0.000 description 1
- 244000263375 Vanilla tahitensis Species 0.000 description 1
- 235000012036 Vanilla tahitensis Nutrition 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005564 crystal structure determination Methods 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000000634 powder X-ray diffraction Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/52—Compounds having —CHO groups bound to carbon atoms of six—membered aromatic rings
- C07C47/575—Compounds having —CHO groups bound to carbon atoms of six—membered aromatic rings containing ether groups, groups, groups, or groups
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/18—Treatment of tobacco products or tobacco substitutes
- A24B15/28—Treatment of tobacco products or tobacco substitutes by chemical substances
- A24B15/30—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances
- A24B15/301—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances by aromatic compounds
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B3/00—Preparing tobacco in the factory
- A24B3/12—Steaming, curing, or flavouring tobacco
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C273/00—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C273/02—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of urea, its salts, complexes or addition compounds
- C07C273/14—Separation; Purification; Stabilisation; Use of additives
- C07C273/16—Separation; Purification
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/02—Salts; Complexes; Addition compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/78—Separation; Purification; Stabilisation; Use of additives
- C07C45/81—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Fats And Perfumes (AREA)
Abstract
本发明公开了一种乙基香兰素共晶化合物,所述共晶化合物由一个乙基香兰素分子和两个尿素分子通过分子间作用力形成基本结构单元,再以基本结构单元重复堆叠形成。本发明还公开了上述乙基香兰素共晶化合物的制备方法及其作为香料在卷烟中的应用。本发明通过将尿素和乙基香兰素混合,形成的乙基香兰素共晶化合物,相比于乙基香兰素单体,有效提高了香料化合物的熔点,因此当将共晶化合物作为香料添加到卷烟中时,能够有效减少香料在常温下的挥发量,即不易挥发,进而提高其稳定性,克服了乙基香兰素单体作为香料存在的易挥发、留香短及抽吸时香气释放不均的问题,乙基香兰素共晶化合物能够实现抽吸时香气的稳定释放,进而提升抽吸者的体验感。
Description
技术领域
本发明涉及一种乙基香兰素共晶化合物,还公开了上述乙基香兰素共晶化合物的制备方法及其作为香料在卷烟中的应用。
背景技术
乙基香兰素具有浓郁的香子兰香气,且是香兰素以及甲基香兰素香气的3-4倍,目前乙基香兰素作为增香剂在奶粉等食品中已有应用,但乙基香兰素单体存在易挥发的问题。目前未见乙基香兰素运用到卷烟加香中的应用。专利Chan.Smoking compositioncontanining an oxalate flavorant-release additive.U.S.A.5172706公开了在卷烟中加入甲基-2-吡嗪基-2-碳酸丙酯的卷烟,在燃烧时能够释放出增香的2-异丙烯基吡嗪。专利Houminer.Smoking composition.U.S.A.4259969公开了一种吡嗪类化合物,在燃吸下,可以释放出烷基吡嗪,增强主流烟气、丰富侧流烟气。专利CN108774211A公开了一种尼古丁共晶、其制备方法及用途,将其添加到电子烟液中,改善了单独添加尼古丁的电子烟在抽吸时的刺激性。
发明内容
发明目的:本发明针对现有技术中乙基香兰素单体作为食品增香剂存在易挥发的问题,提供一种乙基香兰素共晶化合物,还提供上述乙基香兰素共晶化合物的制备方法。
本发明还提供上述乙基香兰素共晶化合物作为增香剂在卷烟中的应用,乙基香兰素共晶化合物作为增香剂用于卷烟加香,能够增加烟草香气的浓郁度,并且香气能够缓慢释放,提升抽吸者的体验感。
技术方案:本发明所述的乙基香兰素共晶化合物,所述共晶化合物由一个乙基香兰素分子和两个尿素分子通过分子间作用力形成基本结构单元,再以基本结构单元重复堆叠形成。乙基香兰素共晶化合物基本结构单元的分子式为[C9H10O3·(CH4N2O)2]。
其中,所述基本结构单元的结构式为:
上述乙基香兰素共晶化合物的制备方法,具体为:称取尿素与乙基香兰素放入反应容器中,加入溶剂后超声溶解,过滤,收集滤液,用封口膜封口并在封口膜上戳小孔若干,室温下溶剂挥发,晶体析出,析出的晶体为乙基香兰素共晶化合物。
其中,乙基香兰素和尿素的加入摩尔比为1:1~1:3。尿素添加量太少,不易析出共晶化合物,尿素添加量太多,析出的可能是尿素原料。
其中,所述溶剂为无水乙醇或甲醇。溶剂的选择原则,是使原料能完全溶解于其中即可。
上述乙基香兰素共晶化合物作为增香剂加入到卷烟中的应用。
其中,将乙基香兰素共晶化合物用无水乙醇溶解完全后加入到烟丝中,乙基香兰素共晶化合物的加入量为烟丝质量的0.5~1%。
本发明乙基香兰素共晶化合物为正交晶系,空间群为Pmna,晶胞参数α=β=γ=90°、其在X射线粉末衍射下,在衍射角2θ为7.1°±0.1°、12.2°±0.1°、14.1°±0.1°、15.3°±0.1°、16.8°±0.1°、18.0°±0.1°、18.3°±0.1°、18.6°±0.1°、21.0°±0.1°、21.6°±0.1°、21.9°±0.1°、24.7°±0.1°、25.6°±0.1°、26.4°±0.1°、27.4°±0.1°、31.0°±0.1°处有特征峰。
有益效果:本发明通过将尿素和乙基香兰素混合,形成的乙基香兰素共晶化合物,相比于乙基香兰素单体,有效提高了香料化合物的熔点,因此当将共晶化合物作为香料添加到卷烟中时,能够有效减少香料在常温下的挥发量,即不易挥发,进而提高其稳定性,克服了乙基香兰素单体作为香料存在的易挥发、留香短及作为卷烟香料抽吸时香气释放不均的问题,乙基香兰素共晶化合物能够实现抽吸时香气的稳定释放,进而提升抽吸者的体验感。
附图说明
图1为本发明乙基香兰素共晶化合物中乙基香兰素分子和尿素分子的结构图;
图2为本发明乙基香兰素共晶化合物局部的链状结构图;
图3为本发明乙基香兰素共晶化合物的晶胞堆积图;
图4为本发明乙基香兰素共晶化合物的PXRD图谱。
具体实施方式
以下结合具体实施例对本发明的技术方案做进一步说明。
实施例1:乙基香兰素共晶化合物的培养(乙基香兰素与尿素的加入摩尔比1∶1)
用分析天平称取乙基香兰素50mg和尿素18mg于50mL小烧杯中,往混合物料中加入15mL无水乙醇,超声至溶解完全,过滤,收集滤液,将收集滤液的烧杯用封口膜进行封口,在封口膜上扎5~6个孔,静置(静置时间两周左右)待晶体析出;两周后,观察到烧杯中出现透明晶状固体,挑出形态较好的晶体,进一步表征分析。
实施例2:乙基香兰素共晶化合物的培养(乙基香兰素与尿素的加入摩尔比1∶3)
用分析天平称取乙基香兰素50mg和尿素54mg于50mL小烧杯中,往混合物料中加入25mL无水乙醇,超声至溶解完全,过滤,收集滤液,将收集滤液的烧杯用封口膜进行封口,在封口膜上扎5~6个孔,静置待晶体析出;两周后,观察到烧杯中出现透明晶状固体,挑出形态较好的晶体,进一步表征分析。
实施例3:以实施例1制得的乙基香兰素共晶化合物作为种子诱导乙基香兰素共晶化合物大量产生
用分析天平称取5g乙基香兰素溶于50mL无水乙醇中,往其中加入1.8g尿素,随后再往其中加入少量实施例1制备的乙基香兰素共晶化合物(这是共晶的扩大制备,加入的少量乙基香兰素共晶化合物作为种子诱导晶体形成,从而得到大量共晶),升温至30℃超声溶解完全(原料量大了,可稍微加热,有助于更快的溶解完全),冷却至室温,静置(静置时间3~4天,通过采用种子诱导能够大大缩短晶体生成时间)待晶体析出,抽滤得大量晶体,洗涤、室温真空干燥,得到透明微黄色晶状固体,产率为70%。
实施例4:实施例3制得的乙基香兰素共晶化合物的晶体结构测定
用SMART APEXⅡ单晶衍射仪在293K下,以Mo Kα射线为入射光源,利用ω扫描技术来收集晶体X射线衍射的数据,在用CrystalClear进行数据处理。晶体结构用SHELXL-2014/7(Sheldrick,2014)直接法来解析,氢原子的位置按照理论加氢确定,非氢原子用各向异性精修,经全矩阵最小二乘法修正偏离因子。相关的晶体数据见表1,并用Diamond和Mercury软件来绘制图2、图3展示的共晶结构图。
表1为乙基香兰素共晶化合物的晶体数据
实施例4:实施例3制得的乙基香兰素共晶化合物的PXRD图谱
使用X射线衍射仪对实施例3制得的微黄色晶状固体进行检测,所得X射线衍射图谱如图4所示。由图4可以看出,该晶体的X射线衍射图谱在衍射角2θ为7.1°±0.1°、12.2°±0.1°、14.1°±0.1°、15.3°±0.1°、16.8°±0.1°、18.0°±0.1°、18.3°±0.1°、18.6°±0.1°、21.0°±0.1°、21.6°±0.1°、21.9°±0.1°、24.7°±0.1°、25.6°±0.1°、26.4°±0.1°、27.4°±0.1°、31.0°±0.1°处有特征峰,再与Mercury软件模拟出的晶体的PXRD图谱相对比,高度相似,说明本发明所制得的共晶化合物为单一的纯相。
实施例5:实施例3制得的乙基香兰素共晶化合物添加到卷烟中的抽吸测评
将乙基香兰素共晶化合物用溶剂溶解后加入到烟丝中,由专业评吸人员评吸,结果如表2所示:
表2为烟丝中添加乙基香兰素共晶化合物(乙基香兰素共晶化合物的加入量为烟丝质量的0.5%)和添加乙基香兰素单体(乙基香兰素单体的加入量为烟丝质量的1%)的卷烟放置2个月的评吸结果
注:每项评价指标满分为10分
从表2的评吸对照结果可知,采用乙基香兰素共晶化合物加香的卷烟存放2个月后,卷烟的香气质量和评吸总分基本无变化,而采用乙基香兰素单体(添加量更多)加香的卷烟对照组在存放2个月后,评吸总分下降2.5分,香气协调性与余味均变差明显。说明乙基香兰素单体加香易挥发,而乙基香兰素共晶化合物可降低香料的挥发损失,延长卷烟的货架期,同时燃吸时香气缓慢均匀释放(因为分子间作用力的存在,所以共晶化合物在点燃后会慢慢裂解,这样香气物质会缓慢释放,起到缓释的效果),抽吸体验感提升。上述实验表明,将乙基香兰素共晶化合物添加到卷烟中,可以提高乙基香兰素的稳定性,使得香气缓慢释放,香气柔和协调,提高抽吸舒适感。
Claims (6)
2.权利要求1所述的乙基香兰素共晶化合物的制备方法,其特征在于,具体为:称取尿素与乙基香兰素放入反应容器中,加入溶剂后超声溶解,过滤,收集滤液,用封口膜封口并在封口膜上戳小孔若干,室温下溶剂挥发,晶体析出,析出的晶体为乙基香兰素共晶化合物。
3.根据权利要求2所述的乙基香兰素共晶化合物的制备方法,其特征在于:乙基香兰素和尿素的加入摩尔比为1:1~1:3。
4.根据权利要求2所述的乙基香兰素共晶化合物的制备方法,其特征在于:所述溶剂为无水乙醇。
5.权利要求1所述的乙基香兰素共晶化合物作为增香剂在卷烟中的应用。
6.根据权利要求5所述的乙基香兰素共晶化合物作为增香剂在卷烟中的应用,其特征在于:将乙基香兰素共晶化合物用无水乙醇溶解完全后加入到烟丝中,乙基香兰素共晶化合物的加入量为烟丝质量的0.5~1%。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110538885.0A CN113336630B (zh) | 2021-05-18 | 2021-05-18 | 一种乙基香兰素共晶化合物及其制备方法和应用 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110538885.0A CN113336630B (zh) | 2021-05-18 | 2021-05-18 | 一种乙基香兰素共晶化合物及其制备方法和应用 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN113336630A CN113336630A (zh) | 2021-09-03 |
CN113336630B true CN113336630B (zh) | 2022-04-26 |
Family
ID=77469121
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202110538885.0A Active CN113336630B (zh) | 2021-05-18 | 2021-05-18 | 一种乙基香兰素共晶化合物及其制备方法和应用 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN113336630B (zh) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114605340B (zh) * | 2022-04-15 | 2023-12-22 | 东南大学 | 一种邻香兰素-吡嗪酰胺共晶及其制备方法 |
CN118221502A (zh) * | 2024-03-14 | 2024-06-21 | 沈阳中科新型肥料有限公司 | 一种丁香酚共晶超分子化合物及其制备方法与应用 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101838188A (zh) * | 2010-05-07 | 2010-09-22 | 中国人民解放军第三军医大学 | 甲基或乙基香兰素的精制方法 |
CN102202522A (zh) * | 2008-10-24 | 2011-09-28 | 罗地亚经营管理公司 | 基于香兰素和乙基香兰素的新化合物及其制备和应用 |
-
2021
- 2021-05-18 CN CN202110538885.0A patent/CN113336630B/zh active Active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102202522A (zh) * | 2008-10-24 | 2011-09-28 | 罗地亚经营管理公司 | 基于香兰素和乙基香兰素的新化合物及其制备和应用 |
CN101838188A (zh) * | 2010-05-07 | 2010-09-22 | 中国人民解放军第三军医大学 | 甲基或乙基香兰素的精制方法 |
Also Published As
Publication number | Publication date |
---|---|
CN113336630A (zh) | 2021-09-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN113336630B (zh) | 一种乙基香兰素共晶化合物及其制备方法和应用 | |
US20220098166A1 (en) | Nicotine salts, co-crystals, and salt co-crystal complexes | |
CN109938396B (zh) | 一种烟草内源性Maillard反应香料的制备方法及在新型烟草制品中的应用 | |
JP2014526278A (ja) | 半透明無煙タバコ製品 | |
LU88711A1 (fr) | Nouveaux composés | |
TWI323641B (en) | Tissues with rich flavonoids of neomarica gracilis and belamcanda chinensis and culture methods for the same | |
US3894543A (en) | Smoking mixture | |
EP3681865A1 (en) | Nicotine salts, co-crystals, and salt co-crystal complexes | |
CN107280065B (zh) | 氨基酸型天然低共熔溶剂烟用保润剂及其制备方法和应用 | |
JPH0453495A (ja) | 粘性多糖類の生産方法 | |
EP3643184A1 (en) | Method for producing tobacco flavor liquid, and tobacco flavor liquid | |
JPS61254127A (ja) | ニチニチソウ器官培養によるインド−ルアルカロイドの製造方法 | |
CN109156881B (zh) | 一种卷烟用薄片形态固体香料及其制备方法与应用 | |
CN114605340B (zh) | 一种邻香兰素-吡嗪酰胺共晶及其制备方法 | |
CN103462207A (zh) | 一种提高辊压法薄片丝感官质量的料液制备方法 | |
CN110584186A (zh) | 一种烟油及其制备方法 | |
US3710512A (en) | Process for preparing licorice extract-like material for tobacco flavoring | |
JP7148743B2 (ja) | (z)型ソラノン、その製造方法および使用 | |
CN109864331A (zh) | 一种卷烟香料添加剂及其制备方法 | |
CN113951557A (zh) | 一种葡萄籽原花青素微粉及其制备方法和应用 | |
CN114525176A (zh) | 一种烟用葫芦巴固体香料及其制备方法和应用 | |
CN113826941A (zh) | 用于电子烟液的微胶囊及其制备方法 | |
JPS6036B2 (ja) | ムラサキ科植物の組織培養方法 | |
CN108863953A (zh) | 一种吡嗪共晶及其制备方法和在卷烟中的应用 | |
CN111039770B (zh) | 一种(e)型茄酮、其制备方法及用途 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
TR01 | Transfer of patent right | ||
TR01 | Transfer of patent right |
Effective date of registration: 20240109 Address after: Building 6, Medical Device Industrial Park, Bowu Modern Industrial Park, Bozhou City, Anhui Province, 236000 Patentee after: Anhui Qiancao Huayan Biotechnology Co.,Ltd. Address before: 211189 No. 2 Southeast University Road, Jiangning District, Nanjing, Jiangsu Patentee before: SOUTHEAST University |