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2,4-二氨基-6-甲基苯酚 | 15872-73-8

中文名称
2,4-二氨基-6-甲基苯酚
中文别名
——
英文名称
4.6-diamino-o-cresol
英文别名
3.5-Diamino-2-oxy-1-methyl-benzol;4.6-Diamino-o-kresol;2,4-diamino-6-methyl-phenol;2,4-diamino-6-methylphenol
2,4-二氨基-6-甲基苯酚化学式
CAS
15872-73-8
化学式
C7H10N2O
mdl
MFCD07189499
分子量
138.169
InChiKey
WSVFDPKNANXQKM-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

计算性质

  • 辛醇/水分配系数(LogP):
    0.6
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.142
  • 拓扑面积:
    72.3
  • 氢给体数:
    3
  • 氢受体数:
    3

ADMET

代谢
来自成年绵羊的瘤胃微生物能够将4,6-二硝基邻甲酚(DNOC)解毒,将这种化合物还原为6-氨基-4-硝基邻甲酚,然后进一步还原为4,6-二氨基邻甲酚。
RUMEN MICROFLORA FROM ADULT SHEEP WERE CAPABLE OF DETOXIFYING 4,6-DINITRO-O-CRESOL (DNOC), REDUCING THIS COMPOUND TO 6-AMINO-4-NITRO-O-CRESOL & THEN TO 4,6-DIAMINO-O-CRESOL.
来源:Hazardous Substances Data Bank (HSDB)
代谢
4,6-二硝基邻甲酚(DNOC)通过口服给予大鼠,其消除速度缓慢,还原是主要的代谢途径。在大鼠和家兔中,DNOC生物转化的主要步骤包括首先是硝基团的还原,随后是乙酰化和/或结合。包括2,4-二氨基-6-甲基苯酚在内的DNOC生物转化产物的可能代谢关系被概述。
4,6-DINITRO-O-CRESOL (DNOC) ADMIN ORALLY TO RATS WAS ELIMINATED SLOWLY, WITH REDN BEING THE MAJOR METABOLIC PATHWAY. IN THE RAT & RABBIT INITIAL REDN OF THE NITRO GROUP, FOLLOWED BY ACETYLATION &/OR CONJUGATION ARE THE MAJOR STEPS INVOLVED IN THE BIOTRANSFORMATION OF DNOC. POSSIBLE METABOLIC RELATION OF THE BIOTRANSFORMATION PRODUCTS, INCLUDING 2,4-DIAMINO-6-METHYLPHENOL, OF DNOC ARE OUTLINED.
来源:Hazardous Substances Data Bank (HSDB)
代谢
2,4-二硝基苯酚及其相应的一元胺衍生物在大鼠盲肠培养物中的代谢被研究。所有化合物都被还原为它们相应的二胺代谢物。结果在讨论二硝基苯酚的比较毒理学时与肠道代谢物有关。
THE METABOLISM OF DINITROPHENOLS & THEIR RESPECTIVE MONOAMINE DERIVATIVES WAS STUDIED IN RAT CECAL INCUBATES. ALL OF THE COMPOUNDS WERE REDUCED TO THEIR CORRESPONDING DIAMINO METABOLITES. THE RESULTS ARE DISCUSSED IN RELATION TO THE COMPARATIVE TOXICOLOGY OF DINITROPHENOLS WITH REGARD TO INTESTINAL METABOLITES.
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 副作用
高铁血红蛋白血症 - 血液中高铁血红蛋白含量增加;该化合物被归类为继发性毒性效应。
Methemoglobinemia - The presence of increased methemoglobin in the blood; the compound is classified as secondary toxic effect
来源:Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
毒理性
  • 非人类毒性摘录
4,6-二氨基邻甲酚(33毫克/千克)或4,6-二氨基-2-仲丁基酚(43毫克/千克)的IP(腹腔注射)给药在15-20分钟内产生了致命的methemoglobinemia(高铁血红蛋白血症)。瘤胃内给药引起了一种不太剧烈的高铁血红蛋白血症。在延长的实验中观察到了溶血和急性肾炎。显然,二氨基酚代谢物是二硝基酚(DNOC或DNBP)中毒时高铁血红蛋白形成的原因。
THE IP ADMIN OF 4,6-DIAMINO-O-CRESOL (33 MG/KG) OR 4,6-DIAMINO-2-SEC-BUTYLPHENOL (43 MG/KG) PRODUCED A LETHAL METHEMOGLOBINEMIA WITHIN 15-20 MINUTES. THE INTRARUMINAL ADMIN INDUCED A LESS DRAMATIC METHEMOGLOBINEMIA. HEMOLYSIS & ACUTE NEPHROSIS WERE OBSERVED IN A PROLONGED EXPERIMENT. APPARENTLY, THE DIAMINOPHENOL METABOLITES ARE RESPONSIBLE FOR THE METHEMOGLOBIN FORMATION IN DINITROPHENOL (DNOC OR DNBP) POISONINGS.
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 非人类毒性摘录
2-甲基-4,6-二硝基酚对绵羊的口服毒性(70毫克/千克)高于2-(1-甲基丙基)-4,6-二硝基酚;然而,呼吸困难和高热是由它们各自的二氨基代谢物,2-甲基-4,6-二氨基酚和2-(1-甲基丙基)-4,6-二氨基酚引起的。这些代谢物还导致了高铁血红蛋白血症、低体温和血液浓缩。
2-METHYL-4,6-DINITROPHENOL SHOWED HIGHER TOXICITY TO SHEEP THAN 2-(1-METHYLPROPYL)-4,6-DINITROPHENOL FOLLOWING ORAL ADMIN (70 MG/KG); HOWEVER, DYSPNEA & HYPERTHERMIA WERE CAUSED BY THEIR RESPECTIVE DIAMINO METABOLITES, 2-METHYL-4,6-DIAMINOPHENOL & 2-(1-METHYLPROPYL)-4,6-DIAMINOPHENOL. THE METABOLITES ALSO CAUSED METHEMOGLOBINEMIA, HYPOTHERMIA, & HEMOCONCENTRATION.
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 非人类毒性摘录
DNOC的二氨代谢物...在体外以5 x 10-4 M的浓度是甲氧基血红蛋白形成的有效诱导剂。在一只山羊腹腔注射2-甲基-4,6-二氨基酚(DAOC)33 mg游离胺/公斤后,几乎立即观察到明显的血红蛋白血症,山羊在45分钟内死亡。同样剂量的DAOC通过瘤胃给药后,出现了较慢且不太明显的甲氧基血红蛋白血症的发展。两种情况下都观察到了血浓缩,后者还发现了溶血和肾病病变。将这两种化合物腹腔注射给猪后,立即产生甲氧基血红蛋白血症,并在1小时内死亡。结果证实了假设,即反刍动物中二硝基酚中毒后的甲氧基血红蛋白血症可能是由二氨基酚代谢物引起的。
Diamino metabolites of DNOC ... were active inducers of methemoglobin formation in vitro at a concentration of 5 x 10-4 M. Marked hemoglobinemia was observed almost immediately in a goat given an intraperitoneal injection of 2-methyl-4,6-diamino phenol (DAOC) at 33 mg free amine/kg, and the goat died within 45 min. A slower and less pronounced development of methemoglobinemia developed following ruminal administration of the same dose of DAOC. Hemoconcentration was observed in both cases, and hemolysis and nephrotic lesions were found in the latter. Intraperitoneal administration of both compounds to pigs produced immediate methemoglobinemia and death within 1 hr. The results confirm the hypothesis that methemoglobinemia following dinitrophenol poisoning in ruminants may be due to the diaminophenol metabolites.
来源:Hazardous Substances Data Bank (HSDB)

安全信息

  • 海关编码:
    2922299090

SDS

SDS:29aa5e03956764e368c63483e55c0407
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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

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Novel Compounds
    摘要:
    本发明涉及一般式I的新化合物,其中A、U、V、X、Y、R1、R2和R3的定义如下所述,其互变异构体、异构体、二对映异构体、对映体、水合物、混合物及其盐以及该盐的水合物,特别是与无机或有机酸或碱形成的生理上可接受的盐,含有这些化合物的药物,它们的用途以及制备它们的方法。
    公开号:
    US20120088755A1
  • 作为产物:
    描述:
    二硝酚氢气 作用下, 以 甲醇 为溶剂, 50.0 ℃ 、200.0 kPa 条件下, 反应 0.25h, 以75%的产率得到2,4-二氨基-6-甲基苯酚
    参考文献:
    名称:
    Pd-Pt /改性GO是一种高效且选择性的多相催化剂,可通过氢源将硝基芳族化合物还原为氨基芳族化合物
    摘要:
    在这项工作中,通过使用固定在改性氧化石墨烯(m- GO)上的Pd-Pt纳米颗粒和氢作为还原源,在50°C的甲醇中,不同的硝基芳族化合物成功地还原为相应的芳族胺,并在甲醇中具有优异的选择性。研究了改性GO上Pd和Pd-Pt负载的催化效率,以还原各种硝基芳族化合物,Pd-Pt / m - GO系统显示出最高的转化率和选择性。该催化剂具有多种技术特征,包括FT-IR,拉曼光谱,UV-Vis,XRD,BET,XPS,FESEM,EDS和TEM。具有小于10nm的尺寸的金属纳米颗粒均匀地分布在米-走。催化剂可以重复使用至少五次而不会失去活性,显示出催化剂结构的稳定性。最后,将制得的催化剂的效率与Pd-Pt / AC和Pd-Pt / GO催化剂进行了比较。
    DOI:
    10.1002/aoc.4832
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文献信息

  • THIOL DYES
    申请人:Eliu Victor Paul
    公开号:US20090113639A1
    公开(公告)日:2009-05-07
    Disclosed are thiol dyes of formula (1), wherein R 1 is hydrogen; C 1 -C 12 alkyl; or phenyl-C 1 -C 4 alkyl; X is C 1 -C 12 alkylene; C 2 -C 12 alkenylene; C 5 -C 10 cycloalkylene; C 5 -C 10 arylene; or C 5 -C 10 arylene-C 1 -C 10 alkylene; Y is the residue of an organic dye which corresponds to the formula (1a), wherein R 2 is hydrogen; or C 1 -C 5 alkyl; R 3 is a radical of formula (1a 1 ): (1a 2 ); or (1a 3 ); or R 2 and R 3 together with the linking carbon atom 1 C form a 6 to 10 membered carbocyclic ring which may optionally be a condensated aromatic system and may contain one or more than one hetero atom; and R 4 , R 5 and R 6 independently form each other are hydrogen, or C 1 -C 5 alkyl; Z is H; or a thio ester group of formula (1b), wherein A is O; S; or N—R9; B is —OR7; —NR7R8, or —SR7; and A is O; S; or N—R 9 ; B is —OR 7 ; —NR 7 R 8 , or —SR 7 ; and R 7 , R 8 and R 9 , independently from each other are hydrogen; C 1 -C 12 alkyl C 6 -C 12 aryl; or C 6 -C 12 aryl-C 1 -C 12 alkyl. The compounds are useful for the dyeing of organic materials, such as keratin fibers, preferably human hair.
    揭示了式(1)的硫醇染料,其中R1为氢;C1-C12烷基;或苯基-C1-C4烷基;X为C1-C12亚烷基;C2-C12烯亚烷基;C5-C10环烷基;C5-C10芳基;或C5-C10芳基-C1-C10亚烷基;Y为与式(1a)对应的有机染料的残基,其中R2为氢;或C1-C5烷基;R3为式(1a1)的基团:(1a2);或(1a3);或R2和R3与连接碳原子1C形成6至10成员的碳环,该碳环可以选择性地是一个缩合芳香系统,并且可以含有一个或多个杂原子;以及R4,R5和R6独立地形成彼此为氢,或C1-C5烷基;Z为H;或式(1b)的硫酯基团,其中A为O;S;或N—R9;B为—OR7;—NR7R8,或—SR7;而A为O;S;或N—R9;B为—OR7;—NR7R8,或—SR7;且R7,R8和R9,彼此独立地为氢;C1-C12烷基;C6-C12芳基;或C6-C12芳基-C1-C12烷基。这些化合物适用于有机材料的染色,例如角蛋白纤维,最好是人类头发。
  • Mixture of Sulfide Dyes
    申请人:Cremer Christian
    公开号:US20090100610A1
    公开(公告)日:2009-04-23
    Disclosed are mixtures of sulfide dyes and dyeing compositions comprising mixtures of sulfide dyes. The dye mixtures are useful for the dyeing of organic materials, such as keratin fibers, preferably human hair.
    揭示了含有硫化染料混合物和含有硫化染料混合物的染料组合物。这些染料混合物适用于有机材料的染色,例如角蛋白纤维,最好是人类头发。
  • Process for Hair Dyeing Comprising Application of Composite Pigment
    申请人:Cremer Christian
    公开号:US20090217465A1
    公开(公告)日:2009-09-03
    Disclosed is a process for dyeing of keratin-containing fibers comprising treating the fibers with at least one functionalized particle comprising on the surface an organic chromophore which is bound via a bridge member, wherein the particles are based on SiO 2 , Al 2 O 3 or mixtures thereof, and the functionalized particles carry a positive charge.
    揭示了一种染色角蛋白含量纤维的方法,包括将纤维与至少一种功能化颗粒处理,该颗粒在表面具有通过桥接成员结合的有机色素,其中颗粒基于SiO2、Al2O3或它们的混合物,并且功能化颗粒带有正电荷。
  • Nitrosulfide dyes
    申请人:Cremer Christian
    公开号:US20090130045A1
    公开(公告)日:2009-05-21
    Disclosed are nitro-sulfide dyes of formula (1), their salts, isomers, hydrates and other solvates, wherein R 1 , R 2 , R 3 , independently from each other are hydrogen; C 1 -C 20 alkyl or C 1 -C 20 alkoxy, which may be substituted by one or more C 1 -C 5 alkoxy, halogen, —NH 2 , mono-C 1 -C 5 alkylamino, di-C 1 -C 5 alkylamino, —NO2 or hydroxy; C 3 -C 6 cycloalkyl; —C(O)H; —C(O)—C 1 -C 5 alkyl; —C(O)OH; —C(O)O—C 1 -C 5 alkyl; halogen; NO 2 ; OH; SH; phenyl, which may be substituted by one or more C 1 -C 5 alkyl, C 1 -C 5 alkoxy, halogen, —NH 2 , mono-C 1 -C 5 alkylamino, di-C 1 -C 5 alkylamino, —NO 2 or hydroxy; or a radical of formula (1a) —NR 4 R 5 , wherein R 4 and R 5 independently from each other are hydrogen; C 1 -C 12 alkyl, which may be substituted by one or more C 1 -C 5 alkyl, C 1 -C 5 -alkoxy, hydroxy or —(CO)—H; —(CO)—C 1 -C 5 alkyl; phenyl or phenyl-C 1 -C 4 alkyl, wherein the phenyl moiety may be substituted by one or more C 1 -C 5 alkyl, C 1 -C 5 alkoxy, halogen, —NH 2 , mono-C 1 -C 5 alkylamino, di-C 1 -C 5 alkylamino, —NO 2 , carboxy or hydroxy; or a radical of formula (2); wherein at least one of the radicals R 1 , R 2 or R 3 is NO 2 ; Y 1 is C 1 -C 10 alkylene; C 5 -C 10 cycloalkylene; C 5 -C 10 arylene; or C 5 -C 10 arylene-(C 1 -C 10 alkylene); Z1 is the direct bond; formula (3); or a cationic biradical of a saturated, aromatic or heteroaromatic group; Q 1 is —C(O)—; —C(O)O—; —OCO—; —N(R 6 )—X 2 —; —CON(R 6 )—; —(R 6 )NC(O)—; —O—; —S—; —S(O)—; or —S(O) 2 —; X 1 and X 2 independently from each other are the direct bond; C 1 -C 10 alkylene; C 5 -C 10 cycloalkylene; C 5 -C 10 arylene; or C 5 -C 10 arylene-(C 1 -C 10 alkylene); and R 6 , R 7 and R 8 independently from each other are hydrogen; C 1 -C 14 alkyl; C 2 -C 14 alkenyl; C 6 -C 10 aryl; C 6 -C 10 aryl-C 1 -C 10 alkyl; or C 1 -C 10 alkyl(C 5 -C 10 aryl); m is 1; or 2; U is hydrogen, if m is 1; or the direct bond, if m is 2; with the proviso that the method does not comprise contacting hair with an enzyme of the type of a protein disulfidisomerase (EC 5.3.4.1). Further, the present invention relates to novel sulfide compounds, compositions thereof, especially comprising other dyes, and to processes for their preparation.
    本发明涉及式(1)的硝基-硫醇染料、其盐、异构体、水合物和其他溶剂化合物,其中R1、R2、R3独立地是氢;C1-C20烷基或C1-C20烷氧基,其可以被一个或多个C1-C5烷氧基、卤素、—NH2、单一C1-C5烷基氨基、双C1-C5烷基氨基、—NO2或羟基取代;C3-C6环烷基;—C(O)H;—C(O)-C1-C5烷基;—C(O)OH;—C(O)O-C1-C5烷基;卤素;NO2;OH;SH;苯基,其可以被一个或多个C1-C5烷基、C1-C5烷氧基、卤素、—NH2、单一C1-C5烷基氨基、双C1-C5烷基氨基、—NO2或羟基取代;或式(1a)的基团—NR4R5,其中R4和R5独立地是氢;C1-C12烷基,其可以被一个或多个C1-C5烷基、C1-C5烷氧基、羟基或—(CO)-H取代;—(CO)-C1-C5烷基;苯基或苯基-C1-C4烷基,其中苯基部分可以被一个或多个C1-C5烷基、C1-C5烷氧基、卤素、—NH2、单一C1-C5烷基氨基、双C1-C5烷基氨基、—NO2、羧基或羟基取代;或式(2)的基团;其中至少一个基团R1、R2或R3是NO2;Y1是C1-C10烷基;C5-C10环烷基;C5-C10芳基;或C5-C10芳基-(C1-C10烷基);Z1是直接键;式(3);或饱和、芳香或杂芳基的阳离子双基团;Q1是—C(O)—;—C(O)O—;—OCO—;—N(R6)—X2—;—CON(R6)—;—(R6)NC(O)—;—O—;—S—;—S(O)—或—S(O)2—;X1和X2独立地是直接键;C1-C10烷基;C5-C10环烷基;C5-C10芳基;或C5-C10芳基-(C1-C10烷基);R6、R7和R8独立地是氢;C1-C14烷基;C2-C14烯基;C6-C10芳基;C6-C10芳基-C1-C10烷基;或C1-C10烷基(C5-C10芳基);m为1或2;U是氢,如果m为1;或直接键,如果m为2;但不包括使用蛋白质二硫酰基异构酶(EC 5.3.4.1)对头发进行接触的方法。此外,本发明还涉及新的硫化物化合物、其组成物,特别是包含其他染料的组成物,以及它们的制备方法。
  • Yellow cationic dyes for dyeing of organic material
    申请人:Eliu Paul Victor
    公开号:US20050000034A1
    公开(公告)日:2005-01-06
    The present invention relates to novel cationic yellow dyes of formula (1) wherein R 1 and R 2 are each independently of the other a C 1 -C 8 alkyl radical or an unsubstituted or substituted benzyl radical, R 3 is hydrogen, C 1 -C 8 alkyl, C 1 -C 8 alkoxy, cyanide or halide, preferably hydrogen and X is an anion, with the proviso that at least one of the substitutents R 1 is a benzyl radical and R 2 is a methyl radical, R 2 is not hydrogen, also to compositions therof, especially comprising other dyes, to processes for the preparation therof and to the use therof in the dyeing of organic material, such as keratin, wool, leather, silk, cellulose or polyamides, especially keratin-containging fibres, cotton or nylon, and preferably human hair.
    本发明涉及一种新型阳离子黄色染料,其化学式为(1),其中R1和R2分别独立地为C1-C8烷基基团或未取代或取代苄基基团,R3为氢、C1-C8烷基、C1-C8烷氧基、氰基或卤素,优选为氢,X为阴离子,但至少有一个取代基R1为苄基基团,而R2为甲基基团,R2不为氢,还涉及其组合物,特别是包含其他染料的组合物,以及其制备方法和在有机材料如角蛋白、羊毛、皮革、丝绸、纤维素或聚酰胺等,特别是角蛋白含量纤维、棉或尼龙,优选为人发染色中的应用。
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(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐