Quick Search
Di-sec-butylamine is a secondary aliphatic amine with two branched sec-butyl groups attached to a single nitrogen atom, giving it a lipophilic structure with significant steric hindrance.
Di-sec-butylamine is a colorless to pale yellow, volatile liquid with a sharp amine-like odor, weakly basic and nucleophilic, forming salts with mineral acids and reacting readily with electrophilic reagents.
Industrially, Di-sec-butylamine is used as an intermediate in the production of rubber chemicals, corrosion inhibitors, surfactants, agrochemicals, and specialty polymers, though it must be handled carefully due to its volatility, flammability, and irritant properties.
CAS Number: 5332-24-1
EC Number: 226-342-2
Molecular Formula: C8H19N
Molar Mass: 129.24 g·mol⁻¹
Synonyms: 2-Butanamine, N- (1-methylpropyl)-, 2-Butanamine, N-(1-methylpropyl)-, 210-937-9, 626-23-3, Bis(1-methylpropyl)amine, bis(butan-2-yl)amine, di-sec-butyl amine, Di-sec-butylamine, MFCD00009326, N-(1-Methylpropyl)-2-butanamine, N-(Butan-2-yl)butan-2-amin, N-(butan-2-yl)butan-2-amine, N-sec-Butyl-2-butanamin, N-sec-Butyl-2-butanamine, N-sec-Butyl-2-butanamine, N-sec-Butylbutan-2-amine, (sec-C4H9)2NH, 1-Propanamine, 1-methyl, N-(1-methylpropyl), 99%, bis(2-methylpropyl)amine, bis(methylpropyl)amine, BIS(SEC-BUTYL)AMINE, butan-2-amine, N-(1-methylpropyl)-, di-s-butylamine, MPBA, N-(Sec-butyl)-2-butanamine, N-butan-2-yl-2-butanamine, N-butan-2-ylbutan-2-amine, 307351_ALDRICH, AI3-28514, MFCD00008930, NSC 8703, NSC8703, TL8004214, DI-SEC-BUTYLAMINE, 626-23-3, 2-Butanamine, N-(1-methylpropyl)-, MPBA, N-butan-2-ylbutan-2-amine, Bis(1-methylpropyl)amine, N-(1-Methylpropyl)-2-butanamine, Di-sec.-butylamine, MFCD00009326, bis(methylpropyl)amine, di-sec-butyl amine, N-sec-butylbutan-2-amine, di-s-butylamine, di-sec.butylamine, di-sec-butyl-amine, NSC 8703, EINECS 210-937-9, bis(butan-2-yl)amine, AI3-28514, butane, 2-s-butylamino-, (sec-C4H9)2NH, butane, 2-sec-butylamino-, bis(1-methyl-propyl)-amine, N-butan-2-yl-2-butanamine, SCHEMBL49755, SCHEMBL49756, N-(Sec-butyl)-2-butanamine #, DTXSID90870719, NSC8703, AAA62623, NSC-8703, SBB059801, AKOS000120370, AKOS017278326, LS-13555, D1604, NS00080672, ST51046071, EN300-20269, 1-Propanamine, 1-methyl, N-(1-methylpropyl), A833893, Q23978210, F2190-0523
Di-sec-butylamine is a secondary aliphatic amine with the molecular formula C₈H₁₉N.
Di-sec-butylamine consists of two sec-butyl groups attached to a single nitrogen atom, giving it a branched, hydrophobic structure.
In its pure form, Di-sec-butylamine appears as a colorless to pale yellow liquid with a strong amine-like odor.
Like other secondary amines, Di-sec-butylamine is both a weak base and a nucleophile, capable of forming salts with mineral acids and reacting readily with electrophilic reagents.
Di-sec-butylamine is used as an intermediate in organic synthesis, particularly in the preparation of rubber chemicals, corrosion inhibitors, and agrochemical products.
Di-sec-butylamine is also employed in the synthesis of surfactants and as a building block in specialty chemicals.
Due to its volatility and strong odor, Di-sec-butylamine must be handled in well-ventilated areas, and contact with skin or eyes should be avoided since it can be irritating.
Di-sec-butylamine's branched alkyl groups contribute to steric hindrance, influencing both its reactivity and solubility compared to straight-chain analogs.
Di-sec-butylamine is a secondary aliphatic amine characterized by the presence of two branched sec-butyl groups attached to the central nitrogen atom.
This structural arrangement gives Di-sec-butylamine both lipophilic properties and significant steric hindrance compared to linear amines, influencing its reactivity and solubility profile.
In its pure form, di-sec-butylamine is typically a clear to pale yellow, volatile liquid with a sharp, penetrating amine-like odor that is common among aliphatic amines.
Di-sec-butylamine has a moderately low boiling point, is miscible with most organic solvents, and shows limited solubility in water due to the bulky hydrocarbon substituents, though it retains the ability to form hydrogen bonds through its nitrogen atom.
From a chemical standpoint, di-sec-butylamine behaves as a weak base and a nucleophile.
Di-sec-butylamine can readily form salts with mineral acids (e.g., hydrochlorides, sulfates) and reacts with a variety of electrophiles in substitution, condensation, and addition reactions.
The steric hindrance of the sec-butyl groups often moderates its reactivity compared to less bulky secondary amines, which can be advantageous in selective synthetic applications.
This property makes Di-sec-butylamine particularly useful as a reagent and intermediate in the fine chemical industry.
In industrial practice, di-sec-butylamine is employed as a versatile intermediate in the synthesis of rubber accelerators, corrosion inhibitors, surfactants, lubricating oil additives, agrochemicals (such as herbicide and pesticide precursors), and specialty polymers.
Di-sec-butylamine may also serve as a building block in pharmaceutical research, where the branched alkyl substituents can influence the lipophilicity and steric characteristics of drug candidates.
From a handling and safety perspective, di-sec-butylamine requires careful management.
Di-sec-butylamine's volatility and strong odor necessitate well-ventilated environments during storage and use.
Direct contact with the liquid or vapors can cause irritation to the skin, eyes, and respiratory system.
Di-sec-butylamine is flammable and should be kept away from ignition sources.
Storage should be in tightly closed containers, protected from moisture, acids, and oxidizing agents to prevent decomposition or hazardous reactions.
In summary, di-sec-butylamine is an important secondary amine with both practical industrial applications and interesting chemical properties arising from its branched sec-butyl substituents.
Di-sec-butylamine's combination of nucleophilicity, basicity, and steric hindrance make it a valuable compound in organic synthesis and applied chemistry, though its handling requires appropriate safety measures due to its volatility, odor, and irritant effects.
Market Overview of Di-Sec-Butylamine:
The global market for Di-sec-butylamine is relatively small compared to other commercial amines, but it plays an important role as a specialty chemical in pharmaceuticals, agrochemicals, lubricants, and surfactants.
Demand for Di-sec-butylamine is primarily driven by its use as an intermediate in the synthesis of herbicides, corrosion inhibitors, and pharmaceutical compounds, with high-purity grades (≥99%) gaining value in fine chemical and drug development applications.
Although exact figures are limited, Di-sec-butylamine's market scale is estimated in the tens of millions of U.S. dollars, with growth projected at around 5–7% CAGR, in line with the broader secondary amine sector.
Asia-Pacific, led by China and India, represents the fastest-growing regional market due to strong agrochemical and industrial production, while Europe and North America maintain steady demand from specialty and pharmaceutical industries.
Challenges such as raw material cost volatility, regulatory constraints, and limited production scale restrain expansion, but opportunities lie in eco-friendly synthesis methods, advanced material applications, and niche high-value markets.
Overall, Di-sec-butylamine occupies a focused yet strategically significant niche within the global amines industry, with long-term potential supported by innovation and industrial diversification.
Uses of Di-Sec-Butylamine:
Di-sec-butylamine is mainly used as a versatile chemical intermediate in the production of a wide range of industrial and specialty chemicals.
In the agrochemical industry, Di-sec-butylamine serves as a precursor for the synthesis of herbicides, pesticides, and plant growth regulators, helping enhance crop protection and yield.
In the pharmaceutical sector, Di-sec-butylamine is employed in the preparation of active pharmaceutical ingredients (APIs) and fine chemical intermediates, where its branched structure can influence the lipophilicity and bioavailability of drug candidates.
Di-sec-butylamine is also used in the manufacture of corrosion inhibitors, which are added to metalworking fluids and industrial systems to extend equipment life, and in the production of surfactants and emulsifiers, which improve the stability and performance of formulations in coatings, lubricants, and detergents.
Additionally, Di-sec-butylamine finds niche applications in the synthesis of specialty polymers and rubber chemicals, where it contributes to enhanced performance characteristics such as flexibility, durability, or resistance to degradation.
Di-sec-butylamine's combination of basicity, nucleophilicity, and steric hindrance makes it an attractive building block for targeted reactions in applied chemistry and industrial manufacturing.
Di-sec-butylamine has a broad spectrum of applications across multiple industries due to its chemical reactivity, steric profile, and ability to act as a building block in the synthesis of more complex compounds.
Di-sec-butylamine's most significant use lies in the agrochemical sector, where it functions as an intermediate in the production of herbicides, pesticides, and plant growth regulators.
The bulky, branched sec-butyl groups of Di-sec-butylamine can modify the chemical properties of agrochemical molecules, improving their stability, environmental persistence, and overall effectiveness in protecting crops against weeds, pests, and diseases.
This makes Di-sec-butylamine a valuable contributor to modern agricultural productivity and crop protection strategies.
In the pharmaceutical industry, Di-sec-butylamine is used as a synthetic intermediate in the preparation of active pharmaceutical ingredients (APIs) and fine chemical derivatives.
Di-sec-butylamine's branched alkyl structure is often exploited to tune the physicochemical properties of drug candidates, such as their solubility, lipophilicity, or metabolic stability.
Through such modifications, Di-sec-butylamine-derived intermediates can improve drug absorption and bioavailability, which are crucial factors in the design of effective medicines.
Beyond pharmaceuticals, Di-sec-butylamine also plays a role in specialty chemical synthesis, where its ability to undergo nucleophilic substitution and addition reactions enables the formation of tailored molecules with diverse industrial applications.
Another important area of application is in corrosion inhibition.
Di-sec-butylamine is incorporated into the formulation of corrosion inhibitors that are added to lubricants, coolants, and metalworking fluids.
These compounds protect metals and alloys from oxidative and chemical damage, thereby extending the life cycle of industrial machinery, pipelines, and automotive systems.
In the surfactant and detergent industry, Di-sec-butylamine is utilized in the synthesis of surface-active agents that enhance wetting, emulsification, and cleaning properties.
Surfactants derived from Di-sec-butylamine improve the performance and stability of products such as industrial cleaners, emulsifiable concentrates, coatings, and even personal care formulations.
In addition, Di-sec-butylamine has applications in the rubber and polymer sectors, where it is employed as a precursor for rubber processing chemicals and as a modifier for specialty polymers.
Di-sec-butylamine's incorporation can lead to improved flexibility, durability, and resistance to oxidative degradation in final polymeric materials.
This makes Di-sec-butylamine useful in the manufacture of specialty rubbers, adhesives, and coatings where performance and longevity are critical.
Finally, Di-sec-butylamine is also studied for its potential role in the development of advanced materials and novel industrial formulations, reflecting the adaptability of its chemical structure.
Overall, the uses of Di-sec-butylamine extend from core industrial applications such as corrosion inhibitors and rubber chemicals to high-value specialty fields including pharmaceuticals and agrochemicals.
Di-sec-butylamine's branched structure, combined with its reactivity as a secondary amine, provides chemists and manufacturers with a flexible tool for designing molecules and materials with optimized functional properties.
Benefits of Di-Sec-Butylamine:
Di-sec-butylamine offers several advantages that make it an attractive compound in industrial chemistry, pharmaceuticals, and agrochemicals.
One of Di-sec-butylamine's key benefits is its role as a versatile intermediate.
Because Di-sec-butylamine is a secondary amine with bulky, branched sec-butyl groups, it combines good nucleophilicity with steric hindrance, allowing for selective reactions in organic synthesis.
This makes Di-sec-butylamine particularly valuable when chemists aim to design molecules with specific physical or biological properties, giving it a distinct edge over simpler linear amines.
In the pharmaceutical industry, Di-sec-butylamine’s benefits are tied to its ability to influence the solubility, lipophilicity, and metabolic stability of drug candidates.
Di-sec-butylamine's incorporation into drug intermediates can improve bioavailability and therapeutic efficiency, leading to more effective pharmaceutical products.
At the same time, Di-sec-butylamine's branched structure reduces excessive reactivity, making it a relatively stable intermediate that is easier to control in multistep synthesis.
For the agrochemical sector, Di-sec-butylamine provides benefits as a precursor to herbicides, pesticides, and plant growth regulators.
The steric effects of its sec-butyl groups contribute to agrochemicals with enhanced stability, longer field persistence, and better resistance to environmental breakdown, which can improve the efficiency of crop protection products.
By helping create more durable formulations, Di-sec-butylamine indirectly supports higher agricultural yields and food security.
Another major benefit lies in the field of corrosion protection and industrial maintenance.
When used in the synthesis of corrosion inhibitors, Di-sec-butylamine contributes to formulations that extend the life of metals, machinery, and pipelines by minimizing oxidative damage and chemical degradation.
This translates into cost savings for industries such as oil and gas, automotive, and manufacturing, where equipment longevity is crucial.
In the surfactant and detergent industry, Di-sec-butylamine-derived compounds enhance emulsification, wetting, and cleaning performance.
This leads to higher-quality industrial cleaners, coatings, and lubricants that perform reliably under demanding conditions.
Similarly, in the rubber and polymer sectors, Di-sec-butylamine adds value by improving the durability, elasticity, and resistance of polymeric materials, making it beneficial in adhesives, specialty rubbers, and protective coatings.
From a broader perspective, another benefit of Di-sec-butylamine is its adaptability for innovation.
Di-sec-butylamine's chemical profile makes it a promising candidate for eco-friendly synthesis methods and advanced applications in specialty chemicals.
Manufacturers who incorporate Di-sec-butylamine in greener production pathways can improve both environmental compliance and market competitiveness.
Production of Di-Sec-Butylamine:
Di-sec-butylamine is not a naturally occurring compound; it is produced industrially through controlled organic synthesis, typically starting from sec-butylamine or sec-butyl halides and combining them with ammonia or other nitrogen sources under specific catalytic conditions.
The general strategy involves introducing two branched sec-butyl groups to a central nitrogen atom, yielding a secondary amine with the desired steric structure.
Amine Alkylation Route:
One common pathway for producing Di-sec-butylamine is alkylation of ammonia or primary amines.
In this method, sec-butyl halides (such as sec-butyl chloride or bromide) or sec-butyl alcohols (after activation) are reacted with ammonia under controlled conditions.
The reaction proceeds stepwise:
Ammonia → sec-butylamine (primary amine)
sec-butylamine + sec-butyl halide → di-sec-butylamine (secondary amine)
Careful control of temperature, pressure, and stoichiometry is required to avoid over-alkylation, which could lead to tri-sec-butylamine or quaternary ammonium salts.
Reductive Amination Route:
Another important method is reductive amination, where sec-butanone (a ketone) reacts with ammonia or a primary amine in the presence of hydrogen and a catalyst such as Raney nickel, palladium, or platinum.
The imine or Schiff base formed in situ is then hydrogenated to yield Di-sec-butylamine.
This method is often preferred because Di-sec-butylamine offers higher selectivity and fewer by-products compared to direct alkylation.
Catalytic Hydrogenation:
In some industrial processes, Di-sec-butylamine can also be prepared by hydrogenation of nitriles derived from sec-butyl precursors.
For example, sec-butyl cyanide can be hydrogenated in the presence of transition-metal catalysts, producing Di-sec-butylamine as the major product under optimized conditions.
By-product Considerations:
During production, undesired by-products such as tri-sec-butylamine (a tertiary amine) and quaternary ammonium salts may form if the reaction is not carefully controlled.
Therefore, fractional distillation or other purification methods are applied to isolate high-purity Di-sec-butylamine (≥99%).
Industrial Scale & Conditions:
Catalysts:
Nickel, palladium, platinum, or copper-based catalysts are commonly used.
Reaction Environment:
High-pressure hydrogenation reactors are employed in reductive amination; alkylation routes often use sealed systems with acid/base catalysts.
Purification:
Distillation under reduced pressure ensures removal of impurities and control of amine content.
Sustainability Trends:
Recent research has focused on green production methods, such as using renewable feedstocks (bio-derived sec-butanol or sec-butylamines), solvent-free conditions, or recyclable catalysts.
This aligns with environmental regulations and demand for sustainable chemical production.
Sythesis of Di-Sec-Butylamine:
Di-sec-butylamine is most commonly synthesized through reductive amination of 2-butanone, where the ketone first reacts with ammonia to form sec-butylamine, and a second reductive amination step with another equivalent of 2-butanone yields the secondary amine.
This process is typically carried out in the presence of hydrogen and metal catalysts such as Raney nickel, palladium on carbon, or platinum, ensuring high selectivity and yield.
Alternatively, Di-sec-butylamine can be prepared by condensing sec-butylamine with 2-butanone to form an imine, followed by catalytic hydrogenation, or through borrowing-hydrogen methods using sec-butanol as the feedstock under transition-metal catalysis.
Direct alkylation routes, where sec-butyl halides react with sec-butylamine, are possible but less efficient due to competing side reactions and over-alkylation to tertiary amines.
After synthesis, the product is purified by fractional distillation under reduced pressure to remove unreacted precursors and by-products, yielding a high-purity Di-sec-butylamine suitable for use in pharmaceuticals, agrochemicals, and specialty chemical applications.
History of Di-Sec-Butylamine:
Di-sec-butylamine does not have a long independent history as a commercial chemical, since it belongs to the broader family of aliphatic secondary amines, which have been known and studied since the late 19th and early 20th centuries.
Early work on amines focused on understanding their basicity, reactivity, and role in forming salts, and by the 1920s–1930s, industrial chemists were already exploring butylamine derivatives (n-butylamine, sec-butylamine, tert-butylamine) as solvents, rubber additives, and intermediates for dyes and pharmaceuticals.
The specific interest in branched amines such as Di-sec-butylamine arose later, in the mid-20th century, when the agrochemical and pharmaceutical industries began requiring more specialized intermediates with unique steric and lipophilic properties.
Secondary amines like Di-sec-butylamine proved valuable for tailoring the biological activity of active ingredients in pesticides, herbicides, and drug molecules.
By the 1960s–1970s, synthetic routes such as reductive amination of 2-butanone and catalytic hydrogenation methods were optimized for both laboratory and industrial production, making Di-sec-butylamine more accessible for research and applied chemistry.
In the late 20th century, as industrial chemistry diversified, Di-sec-butylamine found a role in the production of corrosion inhibitors, lubricants, surfactants, and specialty polymers, aligning with the broader expansion of functionalized amines in applied sectors.
Advances in catalyst technology and hydrogenation methods further improved yields and selectivity, while modern regulatory and environmental pressures have driven interest in green synthesis methods, such as borrowing-hydrogen catalysis and renewable feedstock approaches.
Today, Di-sec-butylamine remains a niche but strategically important compound, used in targeted applications where its branched structure and steric properties provide distinct chemical advantages.
Di-sec-butylamine's history reflects the broader evolution of amine chemistry—from fundamental laboratory studies to industrial applications in agriculture, pharmaceuticals, and materials science.
Handling and Storage of Di-Sec-Butylamine:
Handling:
Work in well-ventilated areas or under a fume hood.
Avoid inhalation of vapors and contact with skin or eyes.
Do not eat, drink, or smoke when handling the material.
Use only in closed systems or with appropriate exhaust ventilation.
Storage:
Store in tightly sealed containers made of compatible materials (stainless steel, HDPE).
Keep in a cool, dry, well-ventilated area away from heat sources, sparks, open flames, acids, and oxidizing agents.
Protect from moisture and direct sunlight.
Recommended storage temperature: ambient to ≤25 °C.
Stability and Reactivity of Di-Sec-Butylamine:
Stability:
Stable under normal temperature and pressure when stored properly.
Reactivity:
Reacts strongly with oxidizing agents (peroxides, nitric acid, etc.) and acids, producing heat and possible hazardous gases.
May corrode some metals.
Decomposition products:
Thermal decomposition may produce nitrogen oxides, carbon monoxide, and carbon dioxide.
Incompatibilities:
Strong oxidizers, strong acids, acid chlorides, and acid anhydrides.
First Aid Measures of Di-Sec-Butylamine:
Inhalation:
Remove person to fresh air.
Keep at rest in a position comfortable for breathing.
If symptoms (cough, dizziness, difficulty breathing) persist, seek medical attention.
Skin contact:
Immediately remove contaminated clothing.
Wash skin thoroughly with soap and water for at least 15 minutes.
Seek medical advice if irritation develops.
Eye contact:
Rinse cautiously with plenty of water for at least 15 minutes.
Remove contact lenses if present and easy to do.
Obtain medical attention immediately.
Ingestion:
Rinse mouth with water.
Do not induce vomiting.
Seek immediate medical care.
Firefighting Measures of Di-Sec-Butylamine:
Suitable extinguishing media:
Alcohol-resistant foam, dry chemical powder, carbon dioxide (CO₂).
Water spray can be used for cooling containers but may not extinguish the fire.
Specific hazards:
Vapors are flammable and may form explosive mixtures with air.
Thermal decomposition can release toxic fumes (NOₓ, CO, CO₂).
Protective equipment:
Firefighters should wear self-contained breathing apparatus (SCBA) and full protective clothing.
Use water spray to cool unopened containers.
Accidental Release Measures of Di-Sec-Butylamine:
Personal precautions:
Evacuate unnecessary personnel.
Ensure adequate ventilation.
Wear appropriate personal protective equipment (PPE).
Remove all ignition sources.
Containment:
Stop leak if safe to do so.
Prevent entry into drains, sewers, or confined areas.
Cleanup methods:
Absorb spill with inert material (vermiculite, sand, earth) and place in suitable containers for disposal.
Wash contaminated surfaces with soap and water.
Dispose of in accordance with local regulations.
Exposure Controls / Personal Protection of Di-Sec-Butylamine:
Engineering controls:
Use local exhaust ventilation or chemical fume hood to maintain airborne concentrations below recommended limits.
Occupational exposure limits (guideline):
No specific limit available; treat as potentially hazardous amine.
Follow general amine exposure guidelines (TWA ~5 ppm where applicable).
Personal protective equipment (PPE):
Respiratory protection:
Use NIOSH-approved organic vapor respirators if ventilation is insufficient.
Eye protection:
Chemical safety goggles or face shield.
Skin protection:
Nitrile, neoprene, or butyl rubber gloves; chemical-resistant clothing or apron.
General hygiene:
Wash hands and exposed skin after handling.
Remove contaminated clothing and wash before reuse.
Identifiers of Di-Sec-Butylamine:
CAS No: 626-23-3
Chemical Name: Di-sec-butylamine
CBNumber: CB7424625
Molecular Formula: C8H19N
Molecular Weight: 129.24
MDL Number: MFCD00009326
IUPAC Name: N-(butan-2-yl)butan-2-amine
Common Name: Di-sec-butylamine
Molecular Formula: C₈H₁₉N
Molar Mass: 129.24 g·mol⁻¹
CAS Number: 5332-24-1
EC Number (EINECS): 226-342-2
Beilstein Registry Number: 1768998
PubChem CID: 138626
ChemSpider ID: 122141
SMILES: CC(C)CN(C)C(C)C
InChI: InChI=1S/C8H19N/c1-5-7(3)9-8(4)6-2/h7-8H,5-6H2,1-4H3
InChI Key: UYTMKNWCVQCUFW-UHFFFAOYSA-N
Linear Formula: [C2H5CH(CH3)]2NH
CAS Number: 626-23-3
Molecular Weight: 129.24
EC Number: 210-937-9
MDL number: MFCD00009326
UNSPSC Code: 12352100
PubChem Substance ID: 24858585
NACRES: NA.22
Properties of Di-Sec-Butylamine:
Melting point: -70°C
Boiling point: 135 °C765 mm Hg(lit.)
Density: 0.753 g/mL at 25 °C(lit.)
refractive index: n20/D 1.41(lit.)
Flash point: 69 °F
pka: pK1:10.91(+1) (25°C)
form: clear liquid
color: Colorless to Almost colorless
LogP: 2.63
Quality Level: 100
Assay: 99%
form: liquid
refractive index: n20/D 1.41 (lit.)
bp: 135 °C/765 mmHg (lit.)
density: 0.753 g/mL at 25 °C (lit.)
functional group: amine
SMILES string: CCC(C)NC(C)CC
InChI: 1S/C8H19N/c1-5-7(3)9-8(4)6-2/h7-9H,5-6H2,1-4H3
InChI key: OBYVIBDTOCAXSN-UHFFFAOYSA-N
Molecular Weight: 129.24 g/mol
XLogP3-AA: 2.4
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 4
Exact Mass: 129.151749610 Da
Monoisotopic Mass: 129.151749610 Da
Topological Polar Surface Area: 12 Ų
Heavy Atom Count: 9
Complexity: 53.6
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 2
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Specifications of Di-Sec-Butylamine:
Appearance: Colorless to Almost colorless clear liquid
Purity(GC): min. 99.0 %
NMR: confirm to structure
