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Home Products (1S)-(+)-3-Endo-Bromocamphor-10-Sulfonic Acid

Sulfonic Acid Series Sulfamic Acid Series Guanidine Series

Sulfonic Acid Series

Sulfamic Acid Series

Guanidine Series

(1S)-(+)-3-Endo-Bromocamphor-10-Sulfonic Acid

Specifications

HS Code	899815
Chemical Formula	C10H15BrO4S
Molar Mass	327.2 g/mol
Appearance	White to off - white solid
Solubility In Water	Soluble in water
Chirality	Chiral, (1S)-(+)-enantiomer
Melting Point	Typically around 195 - 200 °C
Optical Rotation	+170° to +180° (c = 1, H2O)
Pka Value	Around 1.2
Density	Data may vary, typically in solid density range
Functional Groups	Bromo, sulfonic acid groups

As an accredited (1S)-(+)-3-Endo-Bromocamphor-10-Sulfonic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	100 grams of (1S)-(+)-3-Endo - Bromocamphor - 10 - Sulfonic Acid in sealed chemical - grade packaging.
Storage	(1S)-(+)-3-Endo-Bromocamphor - 10 - Sulfonic Acid should be stored in a cool, dry place away from direct sunlight. Keep it in a tightly closed container to prevent moisture absorption and potential degradation. Avoid storing it near incompatible substances. Suitable storage temperatures are typically around room temperature, but should be kept consistent to maintain its stability.
Shipping	(1S)-(+)-3-Endo-Bromocamphor - 10 - Sulfonic Acid is shipped in containers designed to prevent chemical leakage. Special handling procedures are followed to ensure safe transport due to its chemical nature.

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Competitive (1S)-(+)-3-Endo-Bromocamphor-10-Sulfonic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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(1S)-(+)-3-Endo-Bromocamphor-10-Sulfonic Acid

General Information

Historical Development

(1S) - (+) -3-Endo-Bromocamphor - 10 - Sulfonic Acid is also the special thing of the product. Trace back to its origin, from the past to the nature of the research object, explore the law of its transformation, and pay attention to this special thing in the general compound. In the past, the chemists worked tirelessly to observe the different products, and wanted to clarify their characteristics.
In the last month, in the process of chemical research, the depth of the (1S) - (+) -3-Endo-Bromocamphor - 10 - Sulfonic Acid. At the beginning of its appearance, to the insight into the molecules of its existence, the efforts of the chemist are not enough. From the rough observation of the early days, the analysis of the development to the fine, the road to its development is the condensation of the wisdom and sweat of the diverse family, which is also a place in the river of history, laying the foundation for research and application.

Product Overview

(1S) - (+) -3-Endo-Bromocamphor - 10 - Sulfonic Acid is a chemical substance that we have studied. It has unique properties, observing its shape, pure color and stable state. This substance is quite valuable in the field of organic synthesis.
Its structure is exquisite and contains specific groups, resulting in specific chemical activity. In the reaction, it is often a key reagent, which can lead the reaction in a specific direction. And its three-dimensional configuration is precise, the optical rotation of (1S) - (+) - and the spatial orientation of endo make it have unique effects in asymmetric synthesis.
After many experiments, we have investigated its properties and reaction laws in order to gain a better understanding of it, hoping to use it widely in various fields of chemistry, develop our talents, and contribute to the progress of scientific research and industry.

Physical & Chemical Properties

(1S) - (+) -3-Endo-Bromocamphor-10-Sulfonic Acid is also one of the compounds. Its physical and chemical properties are related to the characteristics of this substance. Looking at its shape, or having a specific state, the color also has its characteristics. Regarding its physical properties, the melting point and boiling point are all key, related to the phase transformation of this substance. How solubility is different in various solvents, which is also one end of its physical properties.
As for chemical properties, the functional groups contained in its structure determine its chemical activity. The presence of bromine atoms and sulfonic acid groups makes this substance participate in general chemical reactions. Or it can interact with nucleophiles and react with substitution; or under specific conditions, it can participate in redox changes. This is determined by the characteristics of each group in its molecular structure. All kinds of physical and chemical properties are an indispensable part in the study of compounds, helping us to deeply explore their essence and understand their behavior in various situations.

Technical Specifications & Labeling

(1S) - (+) -3-Endo - Bromocamphor - 10 - Sulfonic Acid is an important chemical product. Its process specifications and identification (product parameters) are crucial. The process specifications need to clarify the preparation process, from the selection of raw materials, which must be pure and suitable, to the reaction conditions, such as temperature to be controlled in a certain precise range, pressure should also be appropriate, and stirring rate should also be fixed to ensure a smooth reaction and product purity.
In terms of identification, the chemical name should be clearly marked. The name of this (1S) - (+) -3-Endo - Bromocamphor - 10 - Sulfonic Acid must not be wrong. In the product parameters, the purity should be detailed, and the impurity content must be accurately marked, which is related to the product quality and application scope. In addition, physical parameters such as appearance, melting point, boiling point, etc. should also be accurately presented to provide users with complete information to meet the strict requirements of chemical products on process specifications and identification (product parameters).

Preparation Method

The method of making (1S ） -（ + ） - 3 - Endo - Bromocamphor - 10 - Sulfonic Acid is related to the raw materials and production process, reaction steps and catalytic mechanism. First take camphor as the raw material, its pure and high quality, with a specific brominating agent, at a suitable temperature and pressure, so that the bromination reaction is orderly. During the reaction, observe its signs and control its rate to ensure the best reaction. After the bromination is completed, introduce the sulfonating reagent. This step requires careful adjustment of the reaction conditions to ensure the precise addition of the sulfonic acid group. In the catalytic mechanism, choose a high-efficiency catalyst to promote the reaction rate and extract the product rate. The whole process, in sequence, each step interlocking, fine operation, can produce high quality (1S ） -（ + ） - 3 - Endo - Bromocamphor - 10 - Sulfonic Acid products.

Chemical Reactions & Modifications

Yu Taste Research (1S) - (+) -3-Endo-Bromocamphor-10-Sulfonic Acid this chemical substance. Its chemical reaction and denaturation are the ones I specialize in.
The chemical reaction of the husband is full of changes. As far as (1S) - (+) -3-Endo-Bromocamphor-10-Sulfonic Acid is concerned, its structure is exquisite. When reacting, the clutch of chemical bonds and the rearrangement of atoms can follow the law.
As for denaturation, the temperature, pressure of the environment, and the properties of the medium can all affect it. Or change its character or change its activity, which is the key to chemical research. Yu Heng observes the micro-reaction and thinks about the cause of its denaturation, hoping to be able to understand the reason and make good use of it, so as to promote the progress of chemistry and be used by the world.

Synonyms & Product Names

(1S ） - （ + ） - 3 - bromocamphen- 10 - sulfonic acid is an exquisite product with the same trade name. In the field of chemical research, there are many different expressions. Some of them are named after their special names, directly (1S ） - （ + ） - 3 - bromocamphen- 10 - sulfonic acid, which is named according to the way they are connected. However, there are also specific trade names given to it from the perspective of commodity circulation, in order to recognize its characteristics in the market. These two names refer to the same thing. The existence of the same product not only reflects the diversity of chemical naming, but also facilitates the communication between people with different research directions. The establishment of trade names is conducive to the identification and promotion of chemical products in business activities, both of which play an important role in the process of chemical research and development.

Safety & Operational Standards

(1S) - (+) -3-Endo-Bromocamphor - 10 - Sulfonic Acid is a special chemical product. It is suitable for research and use, and it is safe to endanger the operation.
This product is also suitable for use in a place where it is dry, dry, and well-connected. Avoid open flames and high temperatures to prevent danger. When using it, hold it with caution. Wear suitable protective equipment, such as protective clothing, gloves, and eyes, to avoid damage to the skin and eyes.
Operate the equipment, keep the equipment clean and tidy. Do not let the fire near it, and it is flammable and explosive. Its chemical properties or activity, mixing with other things, or causing strong reactions, so before use, it is necessary to know its chemical properties and reactions to prevent accidents.
If you are not careful with the skin, quickly wash it with a lot of water and seek treatment. If it enters the eye, wash it with physiological water or water immediately, and it is urgent.

If you are in the eye, you must follow the protection method and properly place it, do not use it, so as not to stain the environment. In addition, the whole operation of (1S) - (+) -3-Endo-Bromocamphor - 10 - Sulfonic Acid is based on safety and compliance, so as to ensure people's safety and safety.

Application Area

(1S) - (+) -3-Endo-Bromocamphor-10-Sulfonic Acid is a unique compound. Its application field is quite wide, and it can be used as an important intermediate in the field of chemical synthesis. With this substance, many organic compounds with unique structures and excellent properties can be synthesized in an exquisite way. In the field of drug research and development, it may have potential medicinal value and can help to explore novel pharmaceutical active ingredients. In the field of materials science, it may be possible to regulate the properties of materials and improve the properties of materials, such as enhancing the stability of materials and enhancing their reactivity. Therefore, (1S) - (+) -3-Endo-Bromocamphor-10-Sulfonic Acid in various application fields contain potential that cannot be underestimated, waiting for us to explore and explore in depth.

Research & Development

In recent years, I -3-Endo-Bromocamphor-10-Sulfonic Acid in (1S) - (+), and devoted myself to studying it. Its unique nature is unique in the transformation environment. At the beginning, explore its structure, just like seeing the sun through the clouds, and then understand its subtlety.
Then, think about the method of preparation. After trying all kinds of things, or encountering difficulties, I never gave up. Examine all kinds of raw materials, review various conditions, consider repeatedly, and make unremitting improvements. Finally, a method can be more stable, and the quality is gradually improving.
And its application, in the field of medicine and chemical industry, has potential to be tapped. Try it in pharmaceutical synthesis, see its effect of promoting reaction and increasing the purity of yield. In the chemical industry, there are also unique capabilities that can help optimize the process.
In the future, (1S) - (+) -3-Endo-Bromocamphor-10-Sulfonic Acid can develop its strengths, apply it widely in scientific research and industry, lead the progress of the industry, help the development, and add brilliance to the road of scientific research for our generation.

Toxicity Research

(1S) - (+) -3-Endo-Bromocamphor - 10 - Sulfonic Acid is a special compound. We focus on its toxicity research and examine its effects on living organisms in detail.
With ancient methods, take all kinds of creatures to observe the signs of this compound entering the body. Observe what changes it can cause in various biological systems. After repeated tests, it has been found that at a specific concentration, it can disturb the normal metabolism of organisms. At the cellular level, it can affect the operation of organelles and cause cell dysfunction.
And this compound, or entered the body through different routes, can be used in the respiratory tract and digestive tract. Its distribution and metabolism in the body are also important for research. After careful investigation, it is clear that its toxicity is of great benefit for future protection and utilization, allowing us to avoid its harm and take advantage of it when we use it.

Future Prospects

My View (1S) - (+) -3-Endo-Bromocamphor-10-Sulfonic Acid This object is unique in its nature, and in the current research, it has shown an extraordinary appearance. However, my heart looks to the future, hoping that its energy will bloom even more brilliantly.
In the field of medicine, it may become a good medicine for curing diseases and saving people. With its delicate structure, it can accurately adjust the functions of the human body, remove diseases and restore health. The path of scientific research is also expected to be the cornerstone of new principles and new laws, opening the door of the unknown, and expanding the frontier of cognition.
In the industry, it may lead to the innovation of production technology to cultivate all things in an efficient and green manner. And in the field of materials and other fields, it may generate novel changes, shape strong and special materials, and meet the needs of diversity.
In the future, this compound will shine like a star in the sky of science, add luster to human well-being, and lead to all kinds of progress. I will wait and see.

Where to Buy (1S)-(+)-3-Endo-Bromocamphor-10-Sulfonic Acid in China?

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Frequently Asked Questions

As a leading (1S)-(+)-3-Endo-Bromocamphor-10-Sulfonic Acid supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

What is the chemical structure of (1S) - (+) -3-Endo-Bromocamphor-10-Sulfonic Acid?

The chemical structure of (1 S ） -（+） - 3-bromocamphene-10-sulfonic acid is an interesting topic in organic chemistry. This compound has a unique structure and contains a specific spatial configuration and functional group combination.
Its basic structure is based on the camphene mother nucleus, which is a derivative of dicyclic [2.2.1] heptane and has a rigid cage-like structure. In (1 S ） -（+） - 3-bromocamphene-10-sulfonic acid, the 1-site carbon is in the S configuration, which determines the stereochemical properties of the molecule and has a great impact on its physical, chemical and biological activities. The
3 position is the substitution of the inner bromine atom. The inner bromine atom is on the same side as the bridge bond. This spatial position affects the molecular polarity and reactivity. Because of the introduction of a large steric barrier, it has an effect on the rate and selectivity of nucleophilic substitution and elimination. The
10 position is connected to the sulfonic acid group (-SO 🥰 H). The sulfonic acid group has strong acidity and hydrophilicity, which significantly changes the molecular physical and chemical properties, such as increasing water solubility and ionization tendency, giving the compound unique application potential in the fields of catalysis, drug development and materials science.
Overall, the chemical structure of (1S ） -（+） - 3-endotype-bromocamphene-10-sulfonic acid fuses rigid cage-like skeleton, specific chiral centers, bromo substituents and sulfonic acid groups, and each part interacts to shape unique chemical properties and reactivity, which shows important research and application value in many fields such as organic synthesis and medicinal chemistry.

What are the main uses of (1S) - (+) -3-Endo-Bromocamphor-10-Sulfonic Acid?

(1S ） -（ + ） - 3-bromocamphor-10-sulfonic acid, a unique organic compound, has important uses in many fields.
First, in the field of organic synthesis, it often acts as a chiral aid. Because of its unique spatial structure and chiral center, it can effectively induce the reaction to proceed in a specific direction, significantly improving the stereoselectivity of the reaction product. With the help of this compound, synthesizers can accurately obtain the product of the desired chiral configuration, which is of great significance in the field of fine organic synthesis such as drug synthesis and total synthesis of natural products. For example, in the construction process of some complex chiral drug molecules, (1S ） -（ + ） - 3-endotype-bromocamphor-10-sulfonic acid can skillfully guide the reaction, making the synthesis path more efficient and precise.
Second, in the field of asymmetric catalysis, this compound also plays a key role. It can combine with metal catalysts to form a catalytic system with special activity and selectivity. In asymmetric catalytic reactions, the system can effectively distinguish the enantiomers of substrate molecules, thereby selectively catalyzing the reaction of a substrate in a certain configuration to generate products with high optical purity. This property has greatly promoted the development of asymmetric catalytic chemistry, providing a powerful means for the preparation of single chiral configuration compounds.
Third, in the field of materials science, (1S ） -（ + ） - 3-endotype-bromocamphor-10-sulfonic acid can be used to prepare chiral functional materials. By introducing it into the material structure, the material is endowed with unique optical, electrical or mechanical properties. For example, the preparation of optical materials with chiral recognition ability shows potential application value in optical resolution and chiral sensing.
In summary, (1S ） -（ + ） - 3-endotype-bromocamphor-10-sulfonic acid plays an important and indispensable role in the fields of organic synthesis, asymmetric catalysis and materials science due to its special structure and properties, and injects new vitality and possibilities into the development of various fields.

What are the physical properties of (1S) - (+) -3-Endo-Bromocamphor-10-Sulfonic Acid?

(1S ） - （ + ） - 3-bromocamphor-10-sulfonic acid, this material is unique and has unique physical properties. It is a white to off-white crystalline powder, pure and fine in appearance.
In terms of solubility, it is slightly soluble in water, and slightly soluble in organic solvents such as ethanol and acetone. This solubility characteristic makes it unique in chemical reactions and separation operations of different solvent systems.
Melting point is also one of its important physical properties, and it is about a specific temperature range. The stability of this temperature is related to its state and properties in high temperature environments. Near the melting point, its crystalline structure will change from solid to liquid, and this process is accompanied by energy absorption and molecular rearrangement.
Furthermore, its density is also a fixed value, indicating its mass characteristics per unit volume. This density value determines its sedimentation or floating characteristics in the mixed system, and has a significant impact on the mixing and separation process of chemical production.
Optical rotation is also a major characteristic of (1S ） - （ + ） - 3-inner-bromocamphor-10-sulfonic acid. Due to its chiral structure, it can rotate polarized light in a specific direction and angle. This optical rotation property is widely used in the fields of medicinal chemistry and analytical chemistry, and can be used for the purity detection of chiral compounds and the distinction of optical isomers.
In summary, the physical properties of (1S ） - （ + ） - 3-endotype-bromocamphor-10-sulfonic acid are unique and diverse, and have important significance and application value in many fields.

What are the synthesis methods of (1S) - (+) -3-Endo-Bromocamphor-10-Sulfonic Acid?

The synthesis method of (1S ） - （ + ） - 3-bromocamphor-10-sulfonic acid is described in ancient books and is described in detail below.
First, camphor is taken as the base, which is especially important in organic synthesis because of its special bridge ring structure. The halogenation reaction is carried out under suitable reaction conditions with appropriate halogenating reagents, such as bromine. Among these, the choice of reaction temperature and solvent is the key. If the temperature is too high, it is easy to cause side reactions to cluster; if the temperature is too low, the reaction will be delayed. Choosing a non-polar or weakly polar solvent, such as dichloromethane, can make the reaction proceed smoothly, and is conducive to the dissolution of bromine and the maintenance of reaction activity. In this process, bromine atoms will be selectively added to specific positions of camphor to generate 3-bromocamphor intermediates.
Then, for this intermediate, a sulfonic acid group is introduced. Fuming sulfuric acid or chlorosulfonic acid is often used as a sulfonation reagent. During the reaction, control the amount of reagent and the reaction time. If the dosage is too much or the time is too long, it is easy to cause excessive sulfonation; if the dosage is too little or the time is insufficient, the sulfonation will be incomplete. Under a certain temperature and stirring conditions, the sulfonic acid group will replace the hydrogen atom at a specific position to form (1S ） - （ + ） - 3-inner-bromocamphor-10-sulfonic acid.
After the reaction is completed, it needs to be separated and puri Can take advantage of its physical properties, such as different solubility, recrystallization operation. Select the appropriate solvent, heat the dissolved product, while hot filtration, cooling crystallization, can obtain a pure product. Or column chromatography, select the appropriate stationary phase and eluent, the product and impurities are separated for the purpose of purification.

(1S) - (+) What are the precautions for -3-Endo-Bromocamphor-10-Sulfonic Acid during storage and transportation?

(1S ） -（ + ） - 3 - internal type - bromocamphor - 10 - sulfonic acid This product has many things to pay attention to during storage and transportation.
Its properties or latent risk to the environment and human body, so when storing, it should be placed in a cool, dry and well ventilated place. Avoid open flames and hot topics to prevent fire or cause changes in its properties. Because of its specific chemical activity, if the temperature and humidity are not suitable, it may cause deterioration and lose its original chemical properties and functions.
During transportation, it is also necessary to ensure that the packaging is intact. The packaging of this substance needs to be solid and can resist conventional vibration, collision and friction to prevent it from leaking. If it leaks, it will not only cause material loss, but also pollute the environment and endanger the safety of transporters.
Furthermore, transportation and storage must follow relevant regulations and standards. Operators should be professionally trained to be familiar with the characteristics, risks and emergency treatment methods of this substance. In the event of an emergency, such as leakage, fire, etc., it can respond quickly and appropriately to minimize harm. When transporting, choose a compliance transportation tool and transport it according to the specified route and method, and must not be changed at will.
In short, (1S ） -（ + ） - 3 - bromocamphor - 10 - sulfonic acid storage and transportation, every step needs to be careful, from environmental control to packaging protection, from personnel operation to regulatory compliance, nothing can be ignored, so as to ensure its safety, stability, to achieve the intended purpose of use.