对甲氨基酚 | 150-75-4

• 分子结构分类: 有机化合物 - 有机氮化合物
• 中文名称: 对甲氨基酚
• 中文别名: P-甲氨基苯酚
• 英文名称: N-methyl-p-aminophenol
• 英文别名: 4-(methylamino)phenol
• CAS: 150-75-4
• 化学式: C₇H₉NO
• mdl: MFCD00042043
• 分子量: 123.155
• InChiKey: ZFIQGRISGKSVAG-UHFFFAOYSA-N

物化性质

• 熔点：
  87 °C
• 沸点：
  262.7±23.0 °C(Predicted)
• 密度：
  1.147±0.06 g/cm3(Predicted)
• 物理描述：
  Colorless solid; [ICSC]
• 颜色/状态：
  Colorless needles
• 溶解度：
  Solubility in water = 11,718 ppm at 25 °C (est)
• 蒸汽压力：
  3.07X10-3 mm Hg at 25 °C
• 亨利常数：
  Henry's Law constant = 4.35X10-10 atm-cu m/mole at 25 °C (est)
• 分解：
  The substance decomposes on burning producing toxic fumes including nitrogen oxides.
• 解离常数：
  pKa = 10.51 (est)

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  9
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.142
• 拓扑面积：
  32.3
• 氢给体数：
  2
• 氢受体数：
  2

ADMET

代谢

在兔体内产生对甲基氨基苯基-β-D-葡萄糖苷酸

Yields p-methylaminophenyl-beta-d-glucuronide in rabbit /From table/

来源:Hazardous Substances Data Bank (HSDB)

毒理性

• 暴露途径

这种物质可以通过摄入被身体吸收。

The substance can be absorbed into the body by ingestion.

来源:ILO-WHO International Chemical Safety Cards (ICSCs)

毒理性

• 皮肤症状

红色。

Redness.

来源:ILO-WHO International Chemical Safety Cards (ICSCs)

毒理性

• 眼睛症状

红肿。疼痛。

Redness. Pain.

来源:ILO-WHO International Chemical Safety Cards (ICSCs)

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；该化合物被归类为次要毒性效应。

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

• 解毒与急救

/SRP:/ 立即急救：确保已经进行了充分的中毒物清除。如果患者停止呼吸，开始人工呼吸，最好使用需求阀复苏器、袋阀面罩装置或口袋面罩，按训练操作。根据需要执行心肺复苏。立即用缓慢流动的水冲洗受污染的眼睛。不要催吐。如果发生呕吐，让患者前倾或置于左侧卧位（如果可能的话，头部向下）以保持呼吸道畅通，防止吸入。保持患者安静，维持正常体温。寻求医疗帮助。 /苯胺及其相关化合物/

/SRP:/ Immediate first aid: Ensure that adequate decontamination has been carried out. If patient is not breathing, start artificial respiration, preferably with a demand-valve resuscitator, bag-valve-mask device, or pocket mask, as trained. Perform CPR as necessary. Immediately flush contaminated eyes with gently flowing water. Do not induce vomiting. If vomiting occurs, lean patient forward or place on left side (head-down position, if possible) to maintain an open airway and prevent aspiration. Keep patient quiet and maintain normal body temperature. Obtain medical attention. /Aniline and related compounds/

来源:Hazardous Substances Data Bank (HSDB)

安全信息

• 危险等级：
  9
• 海关编码：
  2922299090
• 储存条件：
  | 室温 |

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: Sulfuric acid compound with 4-(methylamino)phenol (1:1)
Synonyms:

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Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.

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Section 3. Composition/information on ingredients.
Ingredient name: Sulfuric acid compound with 4-(methylamino)phenol (1:1)
CAS number: 150-75-4

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Section 4. First aid measures
Skin contact: Immediately wash skin with copious amounts of water for at least 15 minutes while removing
contaminated clothing and shoes. If irritation persists, seek medical attention.
Eye contact: Immediately wash skin with copious amounts of water for at least 15 minutes. Assure adequate
flushing of the eyes by separating the eyelids with fingers. If irritation persists, seek medical
attention.
Inhalation: Remove to fresh air. In severe cases or if symptoms persist, seek medical attention.
Ingestion: Wash out mouth with copious amounts of water for at least 15 minutes. Seek medical attention.

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Section 5. Fire fighting measures
In the event of a fire involving this material, alone or in combination with other materials, use dry
powder or carbon dioxide extinguishers. Protective clothing and self-contained breathing apparatus
should be worn.

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Section 6. Accidental release measures
Personal precautions: Wear suitable personal protective equipment which performs satisfactorily and meets local/state/national
standards.
Respiratory precaution: Wear approved mask/respirator
Hand precaution: Wear suitable gloves/gauntlets
Skin protection: Wear suitable protective clothing
Eye protection: Wear suitable eye protection
Methods for cleaning up: Mix with sand or similar inert absorbent material, sweep up and keep in a tightly closed container
for disposal. See section 12.
Environmental precautions: Do not allow material to enter drains or water courses.

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Section 7. Handling and storage
Handling: This product should be handled only by, or under the close supervision of, those properly qualified
in the handling and use of potentially hazardous chemicals, who should take into account the fire,
health and chemical hazard data given on this sheet.
Store in closed vessels.
Storage:

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Section 8. Exposure Controls / Personal protection
Engineering Controls: Use only in a chemical fume hood.
Personal protective equipment: Wear laboratory clothing, chemical-resistant gloves and safety goggles.
General hydiene measures: Wash thoroughly after handling. Wash contaminated clothing before reuse.

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Section 9. Physical and chemical properties
Appearance: Not specified
Boiling point: No data
No data
Melting point:
Flash point: No data
Density: No data
Molecular formula: C7H9NO.H2O4S
Molecular weight: 221.2

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Section 10. Stability and reactivity
Conditions to avoid: Heat, flames and sparks.
Materials to avoid: Oxidizing agents.
Possible hazardous combustion products: Carbon monoxide, nitrogen oxides, sulfur oxides.

---

Section 11. Toxicological information
No data.

---

Section 12. Ecological information
No data.

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Section 13. Disposal consideration
Arrange disposal as special waste, by licensed disposal company, in consultation with local waste
disposal authority, in accordance with national and regional regulations.

---

Section 14. Transportation information
Non-harzardous for air and ground transportation.

---

Section 15. Regulatory information
No chemicals in this material are subject to the reporting requirements of SARA Title III, Section
302, or have known CAS numbers that exceed the threshold reporting levels established by SARA
Title III, Section 313.

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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
  4-羟基苯甲酰胺	N-(4-hydroxyphenyl)formamide	1693-39-6	C7H7NO2	137.138
  N-甲基-P-氨基苯甲醚	N-methyl-N-(4-methoxyphenyl)amine	5961-59-1	C8H11NO	137.181
  对氨基苯酚	4-amino-phenol	123-30-8	C6H7NO	109.128
  1-(对羟基苯基)-2-硫脲	1-(4-hydroxyphenyl)thiourea	1520-27-0	C7H8N2OS	168.219
  N-(4-羟苯基)甘氨酸	N-(hydroxyphenyl)glycine	122-87-2	C8H9NO3	167.164
  N,N-二甲基苯胺	N,N-dimethyl-aniline	86362-18-7	C8H11N	121.182

• 下游产品

  中文名称	英文名称	CAS号	化学式	分子量
  4-二甲氨基苯酚	4-(N,N-dimethylamino)phenol	619-60-3	C8H11NO	137.181
  N-甲基-P-氨基苯甲醚	N-methyl-N-(4-methoxyphenyl)amine	5961-59-1	C8H11NO	137.181
  (4-甲氧基苯基)-二甲胺	4-methoxy-N,N-dimethylanilne	701-56-4	C9H13NO	151.208
  ——	N-methyl-p-phenetidine	3154-18-5	C9H13NO	151.208
  ——	formic acid-(4-hydroxy-N-methyl-anilide)	14924-67-5	C8H9NO2	151.165
  ——	N-Methyl-4-vinyloxy-anilin	2231-73-4	C9H11NO	149.192
  ——	N-methyl-4-(prop-2-yn-1-yloxy)aniline	1178112-51-0	C10H11NO	161.203
  ——	4-(2-methoxyethoxy)-N-methylaniline	——	C10H15NO2	181.235
  N-(4-羟基苯基)-N-甲基-亚硝酸酰胺	N-methyl-N-nitroso-4-hydroxyaniline	2976-94-5	C7H8N2O2	152.153
  ——	4-(4-methylimino)bisphenol	1075742-45-8	C13H13NO2	215.252

反应信息

• 作为反应物：
  描述：

  对甲氨基酚 在 盐酸 、 氢氧化钾 、 sodium tetrahydroborate 、 lithium aluminium tetrahydride 、 三氯化铝 、 sodium 、 四丁基碘化铵 、 对甲苯磺酸 作用下， 以 四氢呋喃 为溶剂， 反应 20.75h， 生成 毒扁豆碱
  参考文献：
  名称：

  Yu, Qian-sheng; Lu, Bao-yuan; Pei, Xue-Feng, Heterocycles, 1994, vol. 39, # 2, p. 519 - 526

  摘要：

  DOI：
• 作为产物：
  描述：

  4-苄氧基-N-甲基苯胺 在 Pd⁽⁰⁾EnCat 、 ammonium formate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 0.17h， 以45%的产率得到对甲氨基酚
  参考文献：
  名称：

  Fast deprotection of phenoxy benzyl ethers in transfer hydrogenation assisted by microwave

  摘要：

  Phenoxy benzyl ethers are easily and quickly deprotected in the presence of ammonium formate and microencapsulated Pd(0)EnCat with the assistance of microwave irradiation. This procedure can be applied in the presence of other functional groups as well. The described protocol is particularly convenient for the preparation in a parallel and automatic fashion of libraries of compounds possessing a phenol type moiety. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2006.12.041

文献信息

• [EN] NEW CATIONIC DYES, KITS AND COMPOSITIONS THEREOF, AND PROCESS FOR DYEING KERATIN FIBERS<br/>[FR] NOUVEAUX COLORANTS CATIONIQUES, KITS ET COMPOSITIONS LES CONTENANT, ET PROCÉDÉ DE TEINTURE DE FIBRES KÉRATINIQUES
  申请人：ALFA PARF GROUP S P A

  公开号：WO2014202150A1

  公开（公告）日：2014-12-24

  The present invention relates to new cationic dyes of general formula (I) and (II): The invention also relates to kits and compositions for dyeing keratin fibers, which contain at least one of these dyes as well as to a process for dyeing keratin fibers using at least one of these dyes.

  本发明涉及一般式(I)和(II)的新阳离子染料：该发明还涉及用于染色角蛋白纤维的套件和组合物，其中至少含有这些染料之一，以及使用至少一种这些染料染色角蛋白纤维的方法。
• Compounds and uses thereof for decreasing activity of hormone-sensitive lipase
  申请人：——

  公开号：US20030166644A1

  公开（公告）日：2003-09-04

  Use of compounds to inhibit hormone-sensitive lipase, pharmaceutical compositions comprising the compounds, methods of treatment employing these compounds and compositions, and novel compounds. The present compounds are inhibitors of hormone-sensitive lipase and may be useful in the treatment and/or prevention of medical disorders where a decreased activity of hormone-sensitive lipase is desirable.

  使用化合物抑制激素敏感性脂肪酶，包括这些化合物的药物组合物，使用这些化合物和组合物的治疗方法，以及新化合物。目前的化合物是激素敏感性脂肪酶的抑制剂，可能在治疗和/或预防需要降低激素敏感性脂肪酶活性的医学疾病中有用。
• Synthesis and pharmacological evaluation of piperidine (piperazine)-amide substituted derivatives as multi-target antipsychotics
  作者：Ling Huang、Lanchang Gao、Xiaohua Zhang、Lei Yin、Jintao Hu、Ting Song、Yin Chen

  DOI：10.1016/j.bmcl.2020.127506

  日期：2020.10

  We report the optimisation of a series of novel amide-piperidine (piperazine) derivatives using the multiple ligand approach with dopamine and serotonin receptors. Of the derivatives, compound 11 exhibited high affinity for the D2, 5-HT1A, and 5-HT2A receptors, but low affinity for the 5-HT2C and histamine H1 receptors and human ether-a-go-go-related gene (hERG) channels. In vivo, compound 11 reduced

  我们报告了与多巴胺和5-羟色胺受体的多配体方法一系列新型酰胺-哌啶（哌嗪）衍生物的优化。在衍生物中，化合物11显示出高亲和力为d 2，5-HT 1A和5-HT 2A受体，但低亲和性对5-HT 2C和组胺H 2 1受体和人ether-A-GO-中间人相关基因（hERG）通道。体内化合物11即使在测试的最高剂量下，阿扑吗啡引起的攀爬，MK-801引起的活动过度和DOI引起的头部抽搐也没有明显的僵直。另外，它在CAR测试中表现出抑制作用。此外，在一个新颖的物体识别任务中，它显示了识别属性。因此，化合物11是有希望的候选多靶点抗精神病药。
• HAIR COLORING COMPOSITIONS
  申请人：——

  公开号：US20020032933A1

  公开（公告）日：2002-03-21

  A hair coloring composition comprising: (a) from about 0.0003 moles (per 100 g of composition) to less than about 0.09 moles (per 100 g of composition) of an inorganic peroxygen oxidizing agent; and (b) an oxidative hair coloring agent; wherein the pH of each of (a) and (b) is in the range of from about 1 to about 6 and wherein the combined mixture of (a) and (b) has a pH in the range of from about 1 to about 6. The products can provide excellent hair coloring and in-use efficacy benefits including excellent initial color and good wash fastness in combination with reduced hair damage at low pH.

  一种染发组合物，包括：(a)约0.0003摩尔（每100克组合物）至约0.09摩尔（每100克组合物）的无机过氧化氧化剂；和(b)氧化性染发剂；其中(a)和(b)的pH值在约1至约6的范围内，且(a)和(b)的混合物的pH值在约1至约6的范围内。该产品可以提供出色的染发效果和使用效果，包括出色的初始颜色和良好的耐洗性，同时在低pH值下减少头发损伤。
• Hair colouring and conditioning compositions
  申请人：The Procter & Gamble Company

  公开号：US20030113286A1

  公开（公告）日：2003-06-19

  A hair colouring and conditioning composition comprising: (a) a hair colouring agent; and (b) a hair conditioning agent; wherein the composition provides an Average Combing Index Value of greater than 1.2 as measured by the Combing Technical Test Method. The products can provide excellent hair colouring together with excellent conditioning, reduced hair damage, brittleness and dryness, and is convenient and easy to use.

  一种包括： (a) 染发剂；和 (b) 护发剂； 的染发和护理组合物； 其中该组合物通过梳理技术测试方法测得的平均梳理指数值大于1.2。 该产品可以提供优秀的染发效果以及优秀的护理效果，减少头发损伤、脆弱和干燥，且使用方便。