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3,5-二甲基-4-氨基苯酚 | 3096-70-6

中文名称
3,5-二甲基-4-氨基苯酚
中文别名
3.5-二甲基-4-胺基苯酚;4-羟基-2,6-二甲基苯胺;4-氨基-3,5-二甲基苯酚;4-氨基-3,5-二甲苯酚
英文名称
3,5-dimethyl-4-aminophenol
英文别名
4-amino-3,5-xylenol;4-amino-3,5-dimethylphenol
3,5-二甲基-4-氨基苯酚化学式
CAS
3096-70-6
化学式
C8H11NO
mdl
MFCD01741459
分子量
137.181
InChiKey
GCWYXRHXGLFVFE-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:
    181 °C
  • 沸点:
    296.5±28.0 °C(Predicted)
  • 密度:
    1.118±0.06 g/cm3(Predicted)
  • 溶解度:
    溶于甲醇
  • 稳定性/保质期:
    遵照规定使用和储存,则不会分解。

计算性质

  • 辛醇/水分配系数(LogP):
    0.7
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    46.2
  • 氢给体数:
    2
  • 氢受体数:
    2

ADMET

代谢
4-羟基-2,6-二甲基苯胺已知的人类代谢物包括(2S,3S,4S,5R)-6-(4-氨基-3,5-二甲基苯氧基)-3,4,5-三羟基氧杂环己烷-2-羧酸。
4-hydroxy-2,6-dimethylaniline has known human metabolites that include (2S,3S,4S,5R)-6-(4-amino-3,5-dimethylphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid.
来源:NORMAN Suspect List Exchange

安全信息

  • 危险品标志:
    N
  • 安全说明:
    S61
  • 危险类别码:
    R50
  • RTECS号:
    ZE6740000
  • 海关编码:
    2922299090
  • 危险性防范说明:
    P261,P280,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H332,H335
  • 储存条件:
    存于阴凉干燥处。

SDS

SDS:52ea788a6fbac7a057b054bae565fc6d
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4-Amino-3,5-xylenol Revision number: 1
SAFETY DATA SHEET

Section 1. BASE INFORMATION
Product name: 4-Amino-3,5-xylenol

Revision number: 1

Section 2. HAZARDS IDENTIFICATION
Classification of the GHS
PHYSICAL HAZARDS Not classified
HEALTH HAZARDS
Category 4
Acute toxicity (Oral)
Acute toxicity (Dermal) Category 4
Category 4
Acute toxicity (Inhalation)
Skin corrosion/irritation Category 2
Category 2A
Serious eye damage/eye irritation
ENVIRONMENTAL HAZARDS Not classified
GHS label elements
Pictograms or hazard symbols
Signal word Warning
Hazard statement Harmful by inhalation, in contact with skin and if swallowed
Causes skin irritation
Causes serious eye irritation
Precautionary statements
[Prevention] Avoid breathing.
Use only outdoors or in a well-ventilated area.
Do not eat, drink or smoke when using this product.
Wash hands thoroughly after handling.
Wear protective gloves and eye/face protection.
IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for
[Response]
breathing. Call a POISON CENTER or doctor/physician if you feel unwell.
IF SWALLOWED: Call a POISON CENTER or doctor/physician if you feel unwell.
Rinse mouth.
IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses,
if present and easy to do. Continue rinsing.
If eye irritation persists: Get medical advice/attention.
IF ON SKIN: Gently wash with plenty of soap and water.
If skin irritation occurs: Get medical advice/attention.
Wash contaminated clothing before reuse.
Call a POISON CENTER or doctor/physician if you feel unwell.
[Disposal] Dispose of contents/container through a waste management company authorized by
the local government
4-Amino-3,5-xylenol

Section 3. COMPOSITION/INFORMATION ON INGREDIENTS
Substance/mixture: Substance
Component(s): 4-Amino-3,5-xylenol
Percent: >98.0%(GC)(T)
CAS Number: 3096-70-6
Synonyms: 4-Amino-3,5-dimethylphenol , 4-Hydroxy-2,6-dimethylaniline
Chemical Formula: C8H11NO

Section 4. FIRST AID MEASURES
Inhalation: Remove victim to fresh air and keep at rest in a position comfortable for breathing.
Call a POISON CENTER or doctor/physician if you feel unwell.
Skin contact: Remove/Take off immediately all contaminated clothing. Gently wash with plenty of
soap and water. If skin irritation or rash occurs: Get medical advice/attention.
Eye contact: Rinse cautiously with water for several minutes. Remove contact lenses, if present
and easy to do. Continue rinsing. If eye irritation persists: Get medical
advice/attention.
Ingestion: Call a POISON CENTER or doctor/physician if you feel unwell. Rinse mouth.
A rescuer should wear personal protective equipment, such as rubber gloves and air-
Protection of first-aiders:
tight goggles.

Section 5. FIRE-FIGHTING MEASURES
Suitable extinguishing Dry chemical, foam, water spray, carbon dioxide.
media:
Specific hazards: Take care as it may decompose upon combustion or in high temperatures to
generate poisonous fume.
Specific methods: Fire-extinguishing work is done from the windward and the suitable fire-extinguishing
method according to the surrounding situation is used. Uninvolved persons should
evacuate to a safe place. In case of fire in the surroundings: Remove movable
containers if safe to do so.
Special protective When extinguishing fire, be sure to wear personal protective equipment.
equipment for firefighters:

Section 6. ACCIDENTAL RELEASE MEASURES
Personal precautions, Use personal protective equipment. Keep people away from and upwind of spill/leak.
protective equipment and Entry to non-involved personnel should be controlled around the leakage area by
emergency procedures: roping off, etc.
Environmental precautions: Prevent product from entering drains.
Methods and materials for Sweep dust to collect it into an airtight container, taking care not to disperse it.
containment and cleaning Adhered or collected material should be promptly disposed of, in accordance with
up: appropriate laws and regulations.

Section 7. HANDLING AND STORAGE
Handling
Technical measures: Handling is performed in a well ventilated place. Wear suitable protective equipment.
Prevent dispersion of dust. Wash hands and face thoroughly after handling.
Use a local exhaust if dust or aerosol will be generated.
Advice on safe handling: Avoid contact with skin, eyes and clothing.
Storage
Storage conditions: Keep container tightly closed. Store in a cool and dark place.
Store under inert gas.
Store away from incompatible materials such as oxidizing agents.
Packaging material: Law is followed.
4-Amino-3,5-xylenol

Section 8. EXPOSURE CONTROLS / PERSONAL PROTECTION
Engineering controls: Install a closed system or local exhaust as possible so that workers should not be
exposed directly. Also install safety shower and eye bath.
Personal protective equipment
Respiratory protection: Dust respirator. Follow local and national regulations.
Hand protection: Protective gloves.
Safety glasses. A face-shield, if the situation requires.
Eye protection:
Skin and body protection: Protective clothing. Protective boots, if the situation requires.

Section 9. PHYSICAL AND CHEMICAL PROPERTIES
Physical state (20°C): Solid
crystal - powder
Form:
Color: White - Greyish reddish yellow
No data available
Odor:
pH: No data available
Melting point/freezing point:181 °C
Boiling Point/Range: No data available
Flash Point: No data available
Explosive limits
No data available
Lower:
Upper: No data available
No data available
Density:
Solubility: Soluble in : Methanol

Section 10. STABILITY AND REACTIVITY
Stability: Stable under proper conditions.
Reactivity: No special reactivity has been reported.
Conditions to avoid: Light-sensitive, Air-sensitive
Incompartible materials: oxidizing agents
Hazardous Decomposition Carbon monoxide, Carbon dioxide, Nitrogen oxides (NOx)
Products:

Section 11. TOXICOLOGICAL INFORMATION
Acute Toxicity: orl-cat LDLo:412 mg/kg
orl-rat LD:>500 mg/kg
Skin corrosion/irritation: No data available
No data available
Serious eye
damage/irritation:
Germ cell mutagenicity: No data available
Carcinogenicity:
No data available
IARC =
NTP = No data available
No data available
Reproductive toxicity:
RTECS Number: ZE6740000

Section 12. ECOLOGICAL INFORMATION
Ecotoxicity:
Fish: No data available
Crustacea: No data available
Algae: No data available
Persistence / degradability: No data available
Bioaccumulative No data available
potential(BCF):
Mobillity in soil
log Pow: No data available
Soil adsorption (Koc): No data available
4-Amino-3,5-xylenol

Section 12. ECOLOGICAL INFORMATION
Henry's Law No data available
constant(PaM3/mol):

Section 13. DISPOSAL CONSIDERATIONS
Recycle to process, if possible. Consult your local regional authorities. You may be able to dissolve or mix material
with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber system.
Observe all federal, state and local regulations when disposing of the substance.

Section 14. TRANSPORT INFORMATION
Hazards Class: Does not correspond to the classification standard of the United Nations
Not Listed
UN-No:

Section 15. REGULATORY INFORMATION
Safe management ordinance of dangerous chemical product (State Council announces on January 26,
2002): Safe use and production, the storage of a dangerous chemical, transport, loading and unloading were
prescribed.


SECTION 16 - ADDITIONAL INFORMATION
N/A

制备方法与用途

用途:用于医药中间体

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
    • 1
    • 2

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    对乙酰氨基酚的毒性机理研究。N-乙酰基-2,6-二甲基和N-乙酰基3,5-二甲基-对苯醌亚胺的合成和反应。
    摘要:
    通过用四乙酸铅氧化由2,6-二甲基对乙酰氨基酚和3,5-二甲基对乙酰氨基酚制备N-乙酰基-2,6-二甲基-对苯醌亚胺和N-乙酰基-3,5-二甲基-对苯醌亚胺。N-乙酰基-2,6-二甲基-对苯醌亚胺与盐酸反应生成3'-氯-2',6'-二甲基-4'-羟基乙酰苯胺,而乙硫醇,苯胺和乙醇生成四面体加合物除了亚胺碳。水得到2,6-二甲基-对苯醌。用N-乙酰基-3,5-二甲基-对苯醌亚胺,水和苯胺取代亚胺碳,生成2,6-二甲基-对苯醌和3,5-二甲基-N-苯基-对苯醌亚胺。乙硫醇得到3'.5'-二甲基-2'-(乙硫基)-4'-羟基乙酰苯胺。2,6-二甲基对乙酰氨基酚和3的毒性,在小鼠和大鼠中组织学检查了5-二甲基对乙酰氨基酚。3,5-二甲基对乙酰氨基酚的肾毒性稍强,但显示出与对乙酰氨基酚相似的肝毒性。2,6-二甲基对乙酰氨基酚与N-甲基对乙酰氨基酚一样,几乎没有组织损伤。
    DOI:
    10.1021/jm00185a001
  • 作为产物:
    描述:
    3,5-Dimethyl-1,4-benzoquinone 4-oxime盐酸 、 tin(ll) chloride 作用下, 以 二氯甲烷 为溶剂, 反应 16.0h, 以90%的产率得到3,5-二甲基-4-氨基苯酚
    参考文献:
    名称:
    对苯醌氮衍生物的狄尔斯-阿尔德反应:实验和理论研究
    摘要:
    对对苯醌和三种氮衍生物的狄尔斯-阿尔德反应的比较反应性和选择性进行了实验和理论研究。单肟衍生物在所测试的反应条件下不反应,而甲苯磺酸化的单肟反应缓慢。然而,单N-甲苯磺酰基亚胺显示出优异的反应性,并且优于母体对-苯醌。DFT计算支持这些实验结果。
    DOI:
    10.1016/j.tet.2014.07.088
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文献信息

  • Copper-Catalyzed Hydroxylation of (Hetero)aryl Halides under Mild Conditions
    作者:Shanghua Xia、Lu Gan、Kailiang Wang、Zheng Li、Dawei Ma
    DOI:10.1021/jacs.6b08114
    日期:2016.10.19
    powerful catalytic system for hydroxylation of (hetero)aryl halides. A wide range of (hetero)aryl chlorides bearing either electron-donating or -withdrawing groups proceeded well at 130 °C, delivering the corresponding phenols and hydroxylated heteroarenes in good to excellent yields. When more reactive (hetero)aryl bromides and iodides were employed, the hydroxylation reactions completed at relatively
    Cu(acac)2 和 N,N'-双(4-羟基-2,6-二甲基苯基)草酰胺 (BHMPO) 的组合为(杂)芳基卤化物的羟基化提供了强大的催化系统。各种带有给电子或吸电子基团的(杂)芳基氯化物在 130 °C 下均能很好地进行,以良好到极好的产率提供相应的酚类和羟基化杂芳烃。当使用反应性更强的(杂)芳基溴化物和碘化物时,羟基化反应在相对较低的温度(分别为 80 和 60 °C)下在低催化负载(0.5 mol% Cu)下完成。
  • Copper-Catalyzed Ullmann-Type Coupling and Decarboxylation Cascade of Arylhalides with Malonates to Access α-Aryl Esters
    作者:Fei Cheng、Tao Chen、Yin-Qiu Huang、Jia-Wei Li、Chen Zhou、Xiao Xiao、Fen-Er Chen
    DOI:10.1021/acs.orglett.1c03688
    日期:2022.1.14
    We have developed a high-efficiency and practical Cu-catalyzed cross-coupling to directly construct versatile α-aryl-esters by utilizing readily available aryl bromides (or chlorides) and malonates. These gram-scale approaches occur with turnovers of up to 1560 and are smoothly conducted by the usage of a low catalyst loading, a new available ligand, and a green solvent. A variety of functional groups
    我们开发了一种高效实用的铜催化交叉偶联,通过利用容易获得的芳基溴化物(或氯化物)和丙二酸盐直接构建多功能的 α-芳基酯。这些克级方法的周转率高达 1560,并且通过使用低催化剂负载、新的可用配体和绿色溶剂顺利进行。可以耐受多种官能团,并且使用 α-芳基酯来获得克级的非甾体抗炎药 (NSAID)。
  • 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。
  • 一种芳基或杂芳基甲氧基化反应的方法
    申请人:五邑大学
    公开号:CN113666826A
    公开(公告)日:2021-11-19
    本发明公开了一种芳基或杂芳基甲氧基化反应的方法。所述方法,包括如下步骤:将底物、偶联剂、配体、溶剂、催化剂和碱混合均匀在惰性气体中反应,得到所述芳基或杂芳基甲氧基化合物。本发明采用价格低廉的卤化亚铜为催化剂,实现了在卤化亚铜催化下,配体调控芳基卤化物或杂芳基卤化物的甲氧基化反应,与现有技术的甲氧基化反应的方法比较,本发明所述方法的反应体系条件温和,催化剂和配体的使用量分别低至底物物质的量的5%,提高了催化效率;且所述方法对不同底物拓展发现对不同官能团的芳基卤化物或杂芳基卤化物有较好的兼容性。采用本发明所述方法制备的芳基或杂芳基甲氧基化合物的产率为36%‑89%。
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