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4-羟基-1,3-苯二磺酸 | 96-77-5

中文名称
4-羟基-1,3-苯二磺酸
中文别名
苯酚-2,4-二磺酸;苯酚二磺酸;5-羟基-4-辛酮
英文名称
4-hydroxy-benzene-1,3-disulfonic acid
英文别名
phenol-2,4-disulfonic acid;phenol-2,4-disulphonic acid;2,4-phenoldisulfonic acid;4-hydroxy-m-benzene disulfonic acid;4-Phenol-1,3-disulfonsaeure;4-Hydroxy-benzol-1,3-disulfonsaeure;Phenol-disulfonsaeure-(2.4);Phenol-2.4-disulfonsaeure;2,4-disulfophenol;Phenoldisulfonic acid;4-hydroxybenzene-1,3-disulfonic acid
4-羟基-1,3-苯二磺酸化学式
CAS
96-77-5
化学式
C6H6O7S2
mdl
MFCD00152742
分子量
254.241
InChiKey
JXBUOZMYKQDZFY-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:
    >99.85°C
  • 沸点:
    367.45°C (rough estimate)
  • 密度:
    1.606 (estimate)

计算性质

  • 辛醇/水分配系数(LogP):
    -1
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    146
  • 氢给体数:
    3
  • 氢受体数:
    7

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:
    IRRITANT
  • 海关编码:
    2908999090
  • 储存条件:
    | 温度范围:2-8°C |

SDS

SDS:a89d0a50bbe8542812bf50d333d570c8
查看
Name: Phenol disulfonic acid solution Material Safety Data Sheet
Synonym: Non
CAS: 96-77-5
Section 1 - Chemical Product MSDS Name:Phenol disulfonic acid solution Material Safety Data Sheet
Synonym:Non

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
96-77-5 Phenol disulfonic acid solution 25% 202-533-6
Hazard Symbols: C
Risk Phrases: 35

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Causes severe burns.Corrosive.Water-reactive.
Potential Health Effects
Eye:
Contact with liquid is corrosive to the eyes and causes severe burns. May cause eye injury.
Skin:
Contact with liquid is corrosive and causes severe burns and ulceration.
Ingestion:
May cause severe gastrointestinal tract irritation with nausea, vomiting and possible burns. May cause corrosion and permanent tissue destruction of the esophagus and digestive tract.
Inhalation:
Causes chemical burns to the respiratory tract. Inhalation may be fatal as a result of spasm, inflammation, edema of the larynx and bronchi, chemical pneumonitis and pulmonary edema.
Chronic:
Repeated inhalation may cause chronic bronchitis. Repeated exposure may cause erosion of teeth.

Section 4 - FIRST AID MEASURES
Eyes: Immediately flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Get medical aid immediately.
Skin:
Get medical aid immediately. Immediately flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and 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.
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. During a fire, irritating and highly toxic gases may be generated by thermal decomposition or combustion. Reacts violently with water.
Extinguishing Media:
Use water spray to cool fire-exposed containers. Use extinguishing media most appropriate for the surrounding fire. If water is the only media available, use in flooding amounts.

Section 6 - ACCIDENTAL RELEASE MEASURES
General Information: Use proper personal protective equipment as indicated in Section 8.
Spills/Leaks:
Clean up spills immediately, observing precautions in the Protective Equipment section. Cover with sand, dry lime or soda ash and place in a closed container for disposal. Isolate area and deny entry. Provide ventilation.

Section 7 - HANDLING and STORAGE
Handling:
Wash thoroughly after handling. Use only in a well-ventilated area.
Avoid contact with clothing and other combustible materials. Do not get on skin or in eyes. Do not ingest or inhale.
Storage:
Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives 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 exhaust ventilation to keep airborne concentrations below the permissible exposure limits.
Exposure Limits CAS# 96-77-5: CAS# 7664-93-9: United States OSHA: 1 mg/m3 TWA Belgium - TWA: 1 mg/m3 VLE Belgium - STEL: 3 mg/m3 VLE France - VME: 1 mg/m3 VME France - VLE: 3 mg/m3 VLE Germany: 0.5 mg/m3 TWA (inhalable fraction, battery manufacture, metal working in a close Japan: 1 mg/m3 Ceiling Malaysia: 1 mg/m3 TWA Netherlands: 1 mg/m3 MAC Russia: 1 mg/m3 TWA Spain: 1 mg/m3 VLA-ED Spain: 3 mg/m3 VLA-EC 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 gloves to prevent skin exposure.
Clothing:
Wear appropriate protective clothing to prevent skin exposure.
Respirators:
Follow the OSHA respirator regulations found in 29 CFR 1910.134 or European Standard EN 149. Use a NIOSH/MSHA or European Standard EN 149 approved respirator if exposure limits are exceeded or if irritation or other symptoms are experienced.

Section 9 - PHYSICAL AND CHEMICAL PROPERTIES

Physical State: Liquid
Color: light pink
Odor: None reported.
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: Not available.
Autoignition Temperature: Not applicable.
Flash Point: Not applicable.
Explosion Limits, lower: Not available.
Explosion Limits, upper: Not available.
Decomposition Temperature:
Solubility in water: Reacts with water.
Specific Gravity/Density: 1.40
Molecular Formula: Mixture
Molecular Weight: 0

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Stable under normal temperatures and pressures.
Conditions to Avoid:
Incompatible materials, combustible materials.
Incompatibilities with Other Materials:
Bases; halides; metals; carbides; chlorates; fulminates; nitrates; picrates; cyanides; alkali halides; nitrites; zinc iodide; permanganates; hydrogen peroxide; azides; perchlorates; nitromethane; phosphorus. Sulfuric acid reacts violently with water; cyclopentadiene; cyclopentanone oxime; nitroaryl amines; hexalithium disilicide; phosphorous (III) oxide.
Hazardous Decomposition Products:
Carbon monoxide, oxides of sulfur, carbon dioxide.
Hazardous Polymerization: Has not been reported

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 96-77-5 unlisted.
CAS# 7664-93-9: WS5600000 LD50/LC50:
Not available.
CAS# 7664-93-9: Draize test, rabbit, eye: 250 ug Severe; Inhalation, mouse: LC50 = 320 mg/m3/2H; Inhalation, mouse: LC50 = 320 mg/m3; Inhalation, rat: LC50 = 510 mg/m3/2H; Inhalation, rat: LC50 = 510 mg/m3; Oral, rat: LD50 = 2140 mg/kg.
Carcinogenicity:
Phenol disulfonic acid solution - Not listed by ACGIH, IARC, or NTP.
Sulfuric acid - ACGIH: A2 - Suspected Human Carcinogen (contained in strong inorg California: carcinogen, initial date 3/14/03 (listed as Strong inorgan NTP: Known carcinogen (listed as Strong inorganic acid mists co IARC: Group 1 carcinogen Other:
See actual entry in RTECS for complete information.

Section 12 - ECOLOGICAL INFORMATION


Section 13 - DISPOSAL CONSIDERATIONS
Products which are considered hazardous for supply are classified as Special Waste and the disposal of such chemicals is covered by regulations which may vary according to location. Contact a specialist disposal company or the local waste regulator for advice. Empty containers must be decontaminated before returning for recycling.

Section 14 - TRANSPORT INFORMATION

IATA
Shipping Name: PHENOLSULPHONIC ACID, LIQUID
Hazard Class: 8
UN Number: 1803
Packing Group: II
IMO
Shipping Name: PHENOLSULPHONIC ACID, LIQUID
Hazard Class: 8
UN Number: 1803
Packing Group: II
RID/ADR
Shipping Name: PHENOLSULPHONIC ACID, LIQUID
Hazard Class: 8
UN Number: 1803
Packing group: II
USA RQ: CAS# 7664-93-9: 1000 lb final RQ; 454 kg final RQ

Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: C
Risk Phrases:
R 35 Causes severe burns.
Safety Phrases:
S 26 In case of contact with eyes, rinse immediately
with plenty of water and seek medical advice.
S 30 Never add water to this product.
S 36/37/39 Wear suitable protective clothing, gloves
and eye/face protection.
WGK (Water Danger/Protection)
CAS# 96-77-5: No information available.
CAS# 7664-93-9: 2
Canada
CAS# 96-77-5 is listed on Canada's NDSL List.
CAS# 7664-93-9 is listed on Canada's DSL List.
CAS# 96-77-5 is not listed on Canada's Ingredient Disclosure List.
CAS# 7664-93-9 is listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 96-77-5 is listed on the TSCA inventory.
CAS# 7664-93-9 is listed on the TSCA inventory.


SECTION 16 - ADDITIONAL INFORMATION
N/A

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:
    4-羟基-1,3-苯二磺酸 作用下, 生成 2,4,6-三氯苯酚
    参考文献:
    名称:
    Datta; Mitter, Journal of the American Chemical Society, 1919, vol. 41, p. 2034
    摘要:
    DOI:
  • 作为产物:
    描述:
    苯酚硫酸 、 sodium hydroxide 作用下, 反应 3.0h, 生成 4-羟基-1,3-苯二磺酸
    参考文献:
    名称:
    基于1,8-萘酐的荧光分子:合成,光谱性质和研究溶液中的电导
    摘要:
    摘要合成了(4-溴-3-硝基-1,8-萘酐)和掺杂剂(4-羟基-间-苯-二磺酸)的化合物。记录化合物的UV-Vis吸收和发射光谱。在浓硫酸和硝酸钠存在下,以4-溴-1,8-萘酐为原料制备化合物(4-溴-3-硝基-1,8-萘酐)。通过在浓硫酸中使用苯酚来制备掺杂剂材料(4-羟基-间苯二磺酸)。吸收带取决于溶剂极性,与乙醇溶剂相比,该化合物在DMSO溶剂中显示出明显的红移。该化合物的荧光光谱对溶剂极性敏感,计算结果表明,在极性溶剂中,最大峰移至红色,移至极性ICT的激发态,从而降低了激发态的能量。研究了掺杂剂材料对化合物电导率(离子和比电导率)的影响,离子电导率随掺杂剂材料重量的增加而增加。
    DOI:
    10.21608/ejchem.2020.18464.2138
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文献信息

  • [EN] METHOD FOR PRODUCING PHENOL AND ACETONE<br/>[FR] PROCÉDÉ DE PRODUCTION DE PHÉNOL ET D'ACÉTONE
    申请人:SABIC INNOVATIVE PLASTICS IP
    公开号:WO2010045423A1
    公开(公告)日:2010-04-22
    A method for producing phenol and acetone in a multi-stage process at an elevated temperature from a cumene hydroperoxide mixture comprising cumene, the method comprising the steps of a) reacting the cumene hydroperoxide mixture with a 2 hydroxybenzenesulfonic acid catalyst having a concentration of 0.1 to 1 mmol/L acid catalyst to form a second mixture comprising phenol, acetone and dicumyl peroxide in a first stage and decomposing the second mixture in a second stage to produce a third mixture comprising phenol and acetone.
    一种在高温下通过多阶段过程从异丙苯过氧化氢混合物中生产苯酚丙酮的方法,所述混合物包括异丙苯,该方法包括以下步骤:a)将异丙苯过氧化氢混合物与浓度为0.1至1毫摩尔/升的2-羟基苯磺酸催化剂反应,形成包括苯酚丙酮和双异丙基过氧化物的第二混合物,并在第二阶段分解第二混合物以产生包括苯酚丙酮的第三混合物。
  • Aromatic sulphonation. Part 93. Sulphonation of the three t-butylphenols, four di-t-butylphenols, and 2,4,6-tri-t-butylphenol
    作者:Hans J. A. Lambrechts、John Mul、Hans Cerfontain
    DOI:10.1039/p29850000677
    日期:——
    The (homogeneous) sulphonation of the three t-butyl-phenols, 2,4-, 2,5-, 2,6-, and 3,5-di-t-butyl-phenol, and 2,4,6-tri-t-butylphenol with a number of sulphonating reagents has been studied, and product compositions have been determined. The formation of the several initial and eventual sulphonation products is explained in terms of sulphodeprotonation, protiode-t-butylation, sulphode-t-butylation
    三种叔丁基苯酚,2,4-,2,5-,2,6-和3,5-二叔丁基苯酚和2,4,6-tri(均一)磺化已经研究了叔丁基苯酚与多种磺化剂的结合,并确定了产品组成。几种初始的和最终的磺化产物的形成是通过磺化质子化,丙醇叔丁基化,硫磺叔丁基化和异构化来解释的,对各种底物都讨论了它们的相对重要性。2-(1)和4-叔丁基苯酚(3),2,4-(4)和2,6-二叔丁基苯酚(6)和2,4,6-三叔丁基苯酚(6)8)在98.5%H 2 SO 4中反应10天后,在35℃下,全部得到50±2%的4-叔丁基苯酚-2,6-(9)和50±2%的苯酚-2,4-二磺酸(10)。对于(1)和(6),起始步骤是叔丁基从2-位快速转移1,3-。然后,对于(1),在2-和6-位进行磺化质子化,对于(6),通过在6-位的丙基叔丁基化,然后在2-和6-位进行磺化质子化。的形成(9从基板)(3),(4)和(8)和(形成10从)(1),(
  • On the intermediacy of phenyl hydrogen sulfates in the sulfonation of phenols. Sulfonation of phenol, anisole, methyl phenyl sulfate, the 2-halogenophenols, a series of phenyl methanesulfonates together with 2,6-dimethylaniline and its N-methylsulfonyl de
    作者:Peter de Wit、Alex F. Woldhuis、Hans Cerfontain
    DOI:10.1002/recl.19881071204
    日期:——
    The sulfonation of methyl phenyl sulfate (4) with concentrated aqueous sulfuric acid at 25°C yields the 4-sulfonic acid. This initial product then decomposes to give phenol-4-sulfonic acid, which is subsequently sulfonated to phenol-2,4-disulfonic acid. From the first-order-rate coefficients obtained for sulfonation of phenyl methanesulfonate (3) and (4) in 93.2% H2SO4, for which acid concentration
    在25℃下用浓硫酸溶液磺化甲基苯基硫酸酯(4),得到4-磺酸。然后该初始产物分解得到苯酚-4-磺酸,随后将其磺化为苯酚-2,4-二磺酸。从在93.2%H 2 SO 4中将甲磺酸苯基酯(3)和(4)磺化所获得的一级系数,对于磺酸浓度为H 2 S 2 O 7的酸浓度,其σp +值OSO 2 Me和OSO 2已确定OMe取代基分别为0.40和0.46。2-氯苯基(10)和2-甲基苯基甲磺酸盐(14)在2.0 °C下在硝基甲烷中用2.0当量的SO 3磺化产生4-磺酸作为排他的产物,而2-甲氧基苯基甲烷磺酸盐(13),在相同条件下,仅形成5-磺酸
  • NMR Characterization of Sulfonation Products of Phenylchloroformate with Verification of NOE Effects by Molecular Modeling
    作者:David Kwoh、Judith L. Kerschner、Arnold Jensen、Anthony Cece
    DOI:10.1366/0003702953964291
    日期:1995.4
    In the trial scale-up of the sulfonation of phenylchloroformate and subsequent formation of sulfonated phenyl carbonates, samples from the batch process showed a number of unexpected by-products. Because they were suspected to have an unusual ring substitution pattern, phenylchloroformate sulfonation was studied by 1H and two-dimensional nuclear magnetic resonance (NMR) techniques. Distance geometry
    在苯氯甲酸酯磺化和随后形成磺化碳酸苯酯的试验放大中,分批过程的样品显示出许多意想不到的副产物。由于怀疑它们具有不寻常的环取代模式,因此通过 1 H 和二维核磁共振 (NMR) 技术研究了苯氯甲酸酯磺化。距离几何用于计算核间距离,用于证实核奥弗豪泽效应的观察。提出了导致这些副产物的反应机理。
  • Feeding habits and dietary overlap in spiny dogfish <i>Squalus acanthias</i> (Squalidae) and narrowmouth catshark <i>Schroederichthys bivius</i> (Scyliorhinidae)
    作者:V.V. Laptikhovsky、A.I. Arkhipkin、A.C. Henderson
    DOI:10.1017/s0025315401004994
    日期:2001.12
    Spiny dogfish Squalus acanthias and narrowmouth catshark Schroederichthys bivius are the only two shark species commonly inhabiting the Falkland Islands shelf. The present study was undertaken to investigate their feeding habits and possible dietary overlap between the species. The diet of the spiny dogfish was dominated by Falkland herring Sprattus fuegensis and squid Loligo gahi, though it also preyed
    多刺角鲨角鲨和窄口猫鲨双鱼鲀是通常栖息在福克兰群岛大陆架上的仅有的两种鲨鱼物种。本研究旨在调查它们的摄食习惯和物种之间可能的饮食重叠。多刺角鲨的饮食以福克兰鲱鱼为主长尾鲩和鱿鱼洛里戈·加希,尽管它也捕食各种其他鱼类和无脊椎动物。猫鲨表现出对无脊椎动物的偏好。这两个物种的饮食随着季节的变化而呈现出显着的变化,个体发生的变化也很明显。食物重叠在冬季最小(15·4%),春季最大(61·1%),后者是由于两个物种都捕食S. fuegensis.
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(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S,S)-邻甲苯基-DIPAMP (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)-(-)-4,12-双(二苯基膦基)[2.2]对环芳烷(1,5环辛二烯)铑(I)四氟硼酸盐 (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)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(4-叔丁基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(3-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-4,7-双(3,5-二-叔丁基苯基)膦基-7“-[(吡啶-2-基甲基)氨基]-2,2”,3,3'-四氢1,1'-螺二茚满 (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 (R)-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 (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 (4S,4''S)-2,2''-亚环戊基双[4,5-二氢-4-(苯甲基)恶唑] (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 (3aR,6aS)-5-氧代六氢环戊基[c]吡咯-2(1H)-羧酸酯 (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-[[[[[((1S,2S)-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 (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 (1S,2S,3R,5R)-2-(苄氧基)甲基-6-氧杂双环[3.1.0]己-3-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 (1-(2,6-二氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙蒿油 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫-d6 龙胆紫