PRODUCTS

OLEYL PROPYLENE DIAMINE

Oleyl Propylene Diamine can be used as dispersing agent, emulsifying agent.
Oleyl Propylene Diamine is used as a catalyst in the production of urethanes and epoxies.
Oleyl Propylene Diamine is used as a emulsifier in the making of asphalt, an ore flotation agent, and a dispersant for some paints.

CAS Number: 7173-62-8
EC Number: 230-528-9
Chemical Name : N-Oleyl-1,3-propylene diamine
Molecular Formula: C21H44N2

SYNONYMS:
1,3-Propanediamine,N1-(9Z)-9-octadecen-1-yl-, 1,3-Propanediamine,N-9-octadecenyl-,(Z)-, 1,3-Propanediamine,N-(9Z)-9-octadecenyl-, N1-(9Z)-9-Octadecen-1-yl-1,3-propanediamine, N-Oleyl-1,3-diaminopropane, N-Oleyl-1,3-propylenediamine, N-Oleyl-1,3-propanediamine, Adogen 572, Diam 11C, Oleylaminopropylamine, Oleyltrimethylenediamine, Dinoram O, Kemamine D 989, N-(3-Aminopropyl)oleylamine, N-Oleyltrimethylenediamine, N-(9-Octadecenyl)-1,3-propylenediamine, Lilamin 572, Diam 11, 3-(Oleylamino)propylamine, Duomeen OL, Diamin OLB, Dicrodamine 1.0, Radiamine 6572, Duomeen OX, N-[cis-9-Octadecenyl]-1,3-propanediamine, N-(9Z-Octadecenyl)-1,3-propylenediamine, 51792-01-9, 648433-31-2, 152725-46-7, N-Oleyl-1,3-propanediamine,Oleyl diamino propane, Oleyl-1,3 diaminopropane, N-Oleyl-1,3-diaminopropane, N-Oleylpropane-1,3-diamine, N-Oleyl-1,3-propylenediamine 1,3-Propanediamine, N-9-octadecenyl-, (Z)-(Z)-N-9-octadecenylpropane-1,3-diamine, N′-octadec-9-enylpropane-1,3-diamine, 3-(oleylamino)propylamine, n-oleyl-1,3-propylenediamine, duomeen ol, diam 11, radiamine 6572, dicrodamine 1.0, diam 11c, n-(3-aminopropyl)oleylamine, 1,3-propanediamine, n-9-octadecenyl-, (z)- (8ci), oleylaminopropylamine, dinoram o, n-oleyl-1,3-propylene, adogen 572, n-(9-octadecenyl)-1,3-propylenediamine, oleyltrimethylenediamine, n-oleyl propane diamine, fentamine da-o, n-oleyl-1,3-propyldiamine, 1,3-propanediamine,n-(9z)-9-octadecenyl- (9ci), n-oleyl-1,3-diaminopropane, kemamine d 989, lilamin 572, duomeen ox, n-oleyltrimethylenediamine, diamin olb, n-[cis-9-octadecenyl]-1,3-propanediamine, n-oleyl-1,3-propanediamine, lilamin572, N-Oleyl-1,3-PropylDiamine,n-oleyl-1,3-propylene,n-oleyl-1,3-propylene diamine, n-oleyl-1,3-propylenediamine,FENTAMINE DA-O,Oleylaminopropylamine,Oleyltrimethylenediamine,Radiamine 6572,Duomeen O from AkzoNobel,DUOMEEN OL from AkzoNobel,N-oleyl-1,3-diaminopropane,(Z)-N-9-octadecenylpropane-1,3-diamine, n-[cis-9-octadecenyl]-1,3-propanediamine, n-oleyltrimethylenediamine, dicrodamine 1.0, radiamine 6572, diam 11, n-(3-aminopropyl)oleylamine, dinoram o, n-oleyl-1,3-propylenediamine, oleylaminopropylamine, n-oleyl-1,3-propanediamine, kemamine d 989, lilamin 572, n-oleyl-1,3-propyldiamine, n-oleyl-1,3-propylene, n-oleyl-1,3-diaminopropane, lilamin572, duomeen ol, duomeen ox, 1,3-propanediamine, n-9-octadecenyl-, (z)- (8ci), 3-(oleylamino)propylamine, adogen 572, oleyltrimethylenediamine, n-oleyl propane diamine, 1,3-propanediamine,n-(9z)-9-octadecenyl- (9ci), fentamine da-o, diamin olb, n-(9-octadecenyl)-1,3-propylenediamine, diam 11c, n-[cis-9-octadecenyl]-1,3-propanediamine, n-oleyltrimethylenediamine, dicrodamine 1.0, radiamine 6572, diam 11, n-(3-aminopropyl)oleylamine, dinoram o, n-oleyl-1,3-propylenediamine, oleylaminopropylamine, n-oleyl-1,3-propanediamine, kemamine d 989, lilamin 572, n-oleyl-1,3-propyldiamine, n-oleyl-1,3-propylene, n-oleyl-1,3-diaminopropane, lilamin572, duomeen ol, duomeen ox, 1,3-propanediamine, n-9-octadecenyl-, (z)- (8ci), 3-(oleylamino)propylamine, adogen 572, oleyltrimethylenediamine, n-oleyl propane diamine, 1,3-propanediamine,n-(9z)-9-octadecenyl- (9ci), fentamine da-o, diamin olb, n-(9-octadecenyl)-1,3-propylenediamine, diam 11c, N-Oleyl-1,3-propanediamine, 7173-62-8, N'-[(Z)-octadec-9-enyl]propane-1,3-diamine, n-oleyl-1,3-propylenediamine, (Z)-N-9-Octadecenylpropane-1,3-diamine, N-OLEYL-1,3-DIAMINOPROPANE, 1,3-Propanediamine, N1-(9Z)-9-octadecen-1-yl-, 54XL96S8SY, 1,3-Propanediamine, N-(9Z)-9-octadecenyl-, 1,3-Propanediamine, N-9-octadecenyl-, (Z)-, 1,3-Propanediamine,N1-(9Z)-9-octadecen-1-yl-, Dinoram O, Radiamine 6572, Lilamin 572, Kemamine D 989, Adogen 572, Diam 11, N-oleyl propane diamine, N-[(9Z)-octadec-9-en-1-yl]propane-1,3-diamine, UNII-54XL96S8SY, EINECS 230-528-9, EC 230-528-9, SCHEMBL197351, DTXSID0027644, TUFJPPAQOXUHRI-KTKRTIGZSA-N, N1-(9Z)-9-Octadecen-1-yl-1,3-propanediamine, A837310, Q27261249, Oleyl diamino propane, Oleyl-1,3 diaminopropane, N-Oleyl-1,3-diaminopropane, N-Oleylpropane-1,3-diamine, N-Oleyl-1,3-propylenediamine, 1,3-Propanediamine, N-9-octadecenyl-, (Z)-, n-[cis-9-octadecenyl]-1,3-propanediamine, n-oleyltrimethylenediamine, dicrodamine 1.0, radiamine 6572, diam 11, n-(3-aminopropyl)oleylamine, dinoram o, n-oleyl-1,3-propylenediamine, oleylaminopropylamine, n-oleyl-1,3-propanediamine, kemamine d 989, lilamin 572, n-oleyl-1,3-propyldiamine, n-oleyl-1,3-propylene, n-oleyl-1,3-diaminopropane, lilamin572, duomeen ol, duomeen ox, 1,3-propanediamine, n-9-octadecenyl-, (z)- (8ci), 3-(oleylamino)propylamine, adogen 572, oleyltrimethylenediamine, n-oleyl propane diamine, 1,3-propanediamine,n-(9z)-9-octadecenyl- (9ci), fentamine da-o, diamin olb, n-(9-octadecenyl)-1,3-propylenediamine, diam 11c, 7173-62-8, 230-528-9, (Z)-N-9-OCTADECENYLPROPANE-1,3-DIAMINE, 1,3-PROPANEDIAMINE, N1-(9Z)-9-OCTADECEN-1-YL-, 1,3-PROPANEDIAMINE, N-9-OCTADECENYL-, (Z)-, ADOGEN 572, DIAM 11, DINORAM O, KEMAMINE D 989, LILAMIN 572, N-OLEYL-1,3-PROPYLENEDIAMINE, RADIAMINE 6572, 3-(oleylamino)propylamine, n-oleyl-1,3-propylenediamine, duomeen ol, diam 11, radiamine 6572, dicrodamine 1.0, diam 11c, n-(3-aminopropyl)oleylamine, 1,3-propanediamine, n-9-octadecenyl-, (z)- (8ci), oleylaminopropylamine, dinoram o, n-oleyl-1,3-propylene, adogen 572, n-(9-octadecenyl)-1,3-propylenediamine, oleyltrimethylenediamine, n-oleyl propane diamine, fentamine da-o, n-oleyl-1,3-propyldiamine, 1,3-propanediamine,n-(9z)-9-octadecenyl- (9ci), n-oleyl-1,3-diaminopropane, kemamine d 989, lilamin 572, duomeen ox, n-[cis-9-octadecenyl]-1,3-propanediamine, n-oleyl-1,3-propanediamine, lilamin572, 7173-62-8

Oleyl Propylene Diamine is an organic compound and a diamine with the formula C21H44N2.
Oleyl Propylene Diamine is an organic compound and a diamine with the formula C21H44N2.
Oleyl Propylene Diamine has found use in numerous industries.

Oleyl Propylene Diamine is an organic compound with the molecular formula C21H44N2.
Oleyl Propylene Diamine is a diamine, meaning it contains two amine groups.
Oleyl Propylene Diamine is characterized by its long hydrocarbon chain derived from oleyl, a monounsaturated fatty acid.

Oleyl Propylene Diamine is typically a colorless or yellow liquid with an ammoniacal odor.
Oleyl Propylene Diamine is insoluble in water but soluble in organic solvents such as acetone and methanol .
Oleylpropylene diamine is similar to Duomeen O.

USES and APPLICATIONS of OLEYL PROPYLENE DIAMINE:
Oleyl Propylene Diamine has found use in numerous industries.
Oleyl Propylene Diamine is used as a catalyst in the production of urethanes and epoxies.
Oleyl Propylene Diamine is used as a emulsifier in the making of asphalt, an ore flotation agent, and a dispersant for some paints.

Oleyl Propylene Diamine has also found use as a lubricant due to its unreactivity with cations, which are present in some adhesive manufacturing.
Oleyl Propylene Diamine is mainly used as Mineral flotation agents, lubricant additive, asphalt emulsifier, coating additives, waterproof agents, chemical intermediates, and so on.

Oleyl Propylene Diamine is widely used in mineral flotation agent,waterproof softener of fiber, dyeing assistant, anti-static agent, pigment dispersant, antirusting agents, anti-caking agent of fertilizer, additives of lubricating oil,germicide,etc.
Application of Oleyl Propylene Diamine is mainly used in asphalt emulsifier, lubricant additive, mineral flotation agent, binder, water-proofing agent, corrosion inhibitor, etc.

Oleyl Propylene Diamine can be used as antistatic agent.
Oleyl Propylene Diamine can be used as corrosion inhibitor agent.
Oleyl Propylene Diamine can be used as dispersing agent, emulsifying agent.

Oleyl Propylene Diamine is used as a catalyst in the production of urethanes and epoxies.
Oleyl Propylene Diamine is used as a emulsifier in the making of asphalt, an ore flotation agent, and a dispersant for some paints.
Oleyl Propylene Diamine has also found use as a lubricant due to its unreactivity with cations, which are present in some adhesive manufacturing.

Oleyl Propylene Diamine uses and applications include: Corrosion inhibitor for metalworking fluids; bitumen emulsifier for car underseals; chemical intermediate; gasoline detergent; flotation agent; antisettling agent for paint formulations; epoxy curing agent; epoxy hardener; bactericide; dispersant in water treatment, pigment flushing, ore flotation; gas, grease, and fuel oil additive

Oleyl Propylene Diamine is mainly used as transport lubricants, corrosion inhibitors, flotation collectors, water treatment catalyst synthesis intermediates, film etc.
Oleyl Propylene Diamine is an intermediate used in the Oilfield and Cleaning industry.

Oleyl Propylene Diamine, otherwise known as N-oleyl-1,3-diaminopropane functions as a Cleansing Surfactant, Corrosion Inhibitor, Dispersing Agent, and for Emulsification purposes.
Application: As antistatic agent, softener, Oleyl Propylene Diamine is widely used in textile, chemical fiber, leather, resin, paint and other fields.

SCIENTIFIC RESEARCH APPLICATIONS OF OLEYL PROPYLENE DIAMINE:
Oleyl Propylene Diamine has a wide range of applications in scientific research and industry:

*Chemistry:
Oleyl Propylene Diamine is used as a catalyst in the production of urethanes and epoxies.

*Biology:
Oleyl Propylene Diamine acts as an emulsifier in biological assays.

*Medicine:
Oleyl Propylene Diamine was investigated for its potential use in drug delivery systems due to its amphiphilic nature.

*Industry:
Oleyl Propylene Diamine is employed as an ore flotation agent, dispersant in paints, and lubricant in adhesive manufacturing.

BENEFITS, USES, AND APPLICATIONS OF OLEYL PROPYLENE DIAMINE:
Oleyl Propylene Diamine is a versatile and efficient chemical compound widely used in various industries such as coatings, adhesives, textiles, and plastics.

This innovative product, Oleyl Propylene Diamine, is specially formulated to provide exceptional performance, offering excellent solubility, low viscosity, and enhanced flexibility.

Its unique chemical structure allows for outstanding adhesion properties, making Oleyl Propylene Diamine suitable for applications requiring strong bonding capabilities.

Moreover, Oleyl Propylene Diamine is designed to improve the durability and resistance of coatings, resulting in enhanced corrosion protection and weathering resistance.

Oleyl Propylene Diamine also enhances the overall mechanical properties of adhesives, textiles, and plastics, making finished products more robust and reliable.

PREPARATION METHODS OF OLEYL PROPYLENE DIAMINE:
*Synthetic Routes and Reaction Conditions
The synthesis of Oleyl Propylene Diamine typically involves the reaction of oleylamine with 1,3-dibromopropane.
The reaction proceeds through a nucleophilic substitution mechanism where the amine group of oleylamine attacks the carbon atoms of 1,3-dibromopropane, displacing the bromine atoms and forming the desired diamine product .

*Industrial Production Methods
Industrial production of Oleyl Propylene Diamine often involves similar synthetic routes but on a larger scale.
The reaction conditions are optimized to ensure high yield and purity of Oleyl Propylene Diamine.

CHEMICAL REACTIONS ANALYSIS OF OLEYL PROPYLENE DIAMINE:
*Types of Reactions
Oleyl Propylene Diamine undergoes various chemical reactions, including:

*Oxidation:
Oleyl Propylene Diamine can be oxidized to form corresponding oxides.

*Reduction:
Oleyl Propylene Diamine can be reduced to form primary amines.

*Substitution:
The amine groups can participate in nucleophilic substitution reactions.

COMMON REAGENTS AND CONDITIONS OF OLEYL PROPYLENE DIAMINE:
*Oxidation:
Common oxidizing agents include hydrogen peroxide and potassium permanganate.

*Reduction:
Reducing agents such as lithium aluminum hydride can be used.

*Substitution:
Halogenated compounds like 1,3-dibromopropane are often used in substitution reactions.

MAJOR PRODUCTS OF OLEYL PROPYLENE DIAMINE:
*Oxidation:
Produces oxides of the original compound.

*Reduction:
Results in primary amines.

*Substitution:
Forms various substituted diamines depending on the reactants used.

COMPARISON WITH SIMILAR COMPOUNDS, OLEYL PROPYLENE DIAMINE:
Similar Compounds
1,3-Diaminopropane:
A simpler diamine with a shorter hydrocarbon chain.

Oleylamine:
Contains a single amine group and a similar hydrocarbon chain.

Uniqueness
Oleyl Propylene Diamine is unique due to its combination of a long hydrocarbon chain and two amine groups.
This structure imparts both hydrophobic and hydrophilic properties, making Oleyl Propylene Diamine versatile in various applications.
Oleyl Propylene Diamine's ability to act as a catalyst, emulsifier, and lubricant sets it apart from simpler diamines and amines .

PROPERTIES OF OLEYL PROPYLENE DIAMINE:
Oleyl Propylene Diamine is a white or slightly yellow solid at ambient temperature,it turns into liquid with slight ammonia smell when heated,soluble in kinds of organic solvents,not soluble in water.
Oleyl Propylene Diamine is organic basicity compounds and can produce salts reacting with acid and will react with carbon dioxide if exposed in air.

Oleyl Propylene Diamine can synthesize nonionic surfactants with ethylene oxide and propylene oxide.
Oleyl Propylene Diamine is used as an asphalt emulsifier.
Oleyl Propylene Diamine is as mineral flotation.

Oleyl Propylene Diamine has a special effect in phosphate rock and other minerals.
Oleyl Propylene Diamine can also be used as a chain lubricant and use in the lubricant additive industry.
Oleyl Propylene Diamine is as pigment dispersing agent in the pigment industry.

MECHANISM OF ACTION OF OLEYL PROPYLENE DIAMINE:
*Target of Action
Oleyl Propylene Diamine is an organic compound and a diamine with the formula C21H44N2 .
Oleyl Propylene Diamine is primarily targeted in the production of urethanes and epoxies, serving as a catalyst .
Oleyl Propylene Diamine also targets the manufacturing process of asphalt, acting as an emulsifier .

*Mode of Action
Oleyl Propylene Diamine interacts with its targets by promoting chemical reactions.
For instance, Oleyl Propylene Diamine acts as a catalyst in the production of urethanes and epoxies, accelerating the reaction process.
Oleyl Propylene Diamine also serves as an emulsifier in the making of asphalt, facilitating the mixing of water and oil-based components .

*Biochemical Pathways
The biochemical pathways affected by Oleyl Propylene Diamine are primarily related to the synthesis of urethanes, epoxies, and asphalt.
Oleyl Propylene Diamine’s role as a catalyst and emulsifier influences these pathways, leading to the successful production of the aforementioned materials.

*Result of Action
The molecular and cellular effects of Oleyl Propylene Diamine’s action are most evident in its role as a catalyst and emulsifier.
Oleyl Propylene Diamine facilitates chemical reactions in the production of urethanes and epoxies, and promotes the mixing of disparate substances in the creation of asphalt.

*Action Environment
Environmental factors can influence the action, efficacy, and stability of Oleyl Propylene Diamine.
For instance, Oleyl Propylene Diamine is stable under normal conditions but can oxidize under certain circumstances .
Oleyl Propylene Diamine’s also worth noting that this compound is biodegradable, indicating that it can be broken down by biological organisms in the environment .

BIOCHEMICAL ANALYSIS OF OLEYL PROPYLENE DIAMINE:
*Biochemical Properties
Oleyl Propylene Diamine is used as a catalyst in the production of urethanes and epoxies .
Oleyl Propylene Diamine interacts with enzymes and proteins involved in these reactions, facilitating the formation of the desired products .

*Cellular Effects
The effects of Oleyl Propylene Diamine on cells are largely dependent on its role in the biochemical reactions it catalyzes.
As a catalyst, Oleyl Propylene Diamine can influence cell function by accelerating the rate of these reactions .

*Molecular Mechanism
The molecular mechanism of Oleyl Propylene Diamine involves its interaction with enzymes and proteins.
As a catalyst, Oleyl Propylene Diamine lowers the activation energy of the reactions it is involved in, thereby increasing the rate of these reactions .

*Temporal Effects in Laboratory Settings
The effects of Oleyl Propylene Diamine in laboratory settings can change over time due to factors such as its stability and degradation .

*Metabolic Pathways
Oleyl Propylene Diamine is involved in the metabolic pathways of urethanes and epoxies .
Oleyl Propylene Diamine interacts with enzymes and cofactors in these pathways, influencing metabolic flux and metabolite levels .

PHYSICAL and CHEMICAL PROPERTIES of OLEYL PROPYLENE DIAMINE:
Molecular Weight: 324.6 g/mol
XLogP3-AA: 7.1
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 19
Exact Mass: 324.350449412 g/mol
Monoisotopic Mass: 324.350449412 g/mol
Topological Polar Surface Area: 38Å²
Heavy Atom Count: 23
Formal Charge: 0
Complexity: 226
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0

Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 1
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
CAS No.: 7173-62-8
UN No.: 2922
Molecular Formula: C21H44N2
InChIKeys: InChIKey=TUFJPPAQOXUHRI-KTKRTIGZSA-N
Molecular Weight: 324.58746
Exact Mass: 324.59
EC Number: 230-528-9

PSA: 38.05000
XLogP3: 7.05350
Density: 0.851 g/cm3
Boiling Point: 435.6ºC at 760 mmHg
Flash Point: 257.5ºC
Refractive Index: 1.464
CAS RN: 7173-62-8
Product Name: N-Oleyl-1,3-propanediamine
Molecular Formula: C21H44N2
Molecular Weight: 324.6 g/mol
IUPAC Name: N'-[(Z)-octadec-9-enyl]propane-1,3-diamine
InChI: InChI=1S/C21H44N2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20-23-21-18-19-22/h9-10,23H,2-8,11-22H2,1H3/b10-9-

InChI Key: TUFJPPAQOXUHRI-KTKRTIGZSA-N
Isomeric SMILES: CCCCCCCC/C=CCCCCCCCCNCCCN
SMILES: CCCCCCCCC=CCCCCCCCCNCCCN
Canonical SMILES: CCCCCCCCC=CCCCCCCCCNCCCN
Other CAS RN: 7173-62-8
Physical Description: Liquid
Boiling point: 435.6±28.0 °C(Predicted)
Density: 0.851±0.06 g/cm3(Predicted)
vapor pressure: 0.002 Pa at 20℃
pka: 10.67±0.19(Predicted)
Water Solubility: 36mg/L at 23℃

LogP: 0
Indirect Additives used in Food Contact Substances: N-OLEYL-1,3-PROPYLENEDIAMINE
FDA UNII: 54XL96S8SY
EPA Substance Registry System: N-Oleyl-1,3-propanediamine (7173-62-8)
Molecular Weight: 324.59
Molecular Formula: C21H44N2
Canonical SMILES: CCCCCCCCC=CCCCCCCCCNCCCN
InChI Key: TUFJPPAQOXUHRI-KTKRTIGZSA-N
Boiling Point: 435.6ºC at 760 mmHg
Flash Point: 257.5ºC
Density: 0.851 g/cm³
EC Number: 230-528-9
Exact Mass: 324.35000

CAS Number: 7173-62-8
Molecular Weight: 324.58700
Density: 0.851 g/cm3
Boiling Point: 435.6ºC at 760 mmHg
Molecular Formula: C21H44N2
Melting Point: N/A
MSDS: N/A
Flash Point: 257.5ºC
Density: 0.851 g/cm3
Boiling Point: 435.6ºC at 760 mmHg
Molecular Formula: C21H44N2
Molecular Weight: 324.58700

Flash Point: 257.5ºC
Exact Mass: 324.35000
PSA: 38.05000
LogP: 7.05350
Index of Refraction: 1.464
IUPAC Name: N'-[(Z)-octadec-9-enyl]propane-1,3-diamine
InChI: InChI=1S/C21H44N2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20-23-21-18-19-22/h9-10,23H,2-8,11-22H2,1H3/b10-9-
InChI Key: TUFJPPAQOXUHRI-KTKRTIGZSA-N
Canonical SMILES: CCCCCCCCC=CCCCCCCCCNCCCN
Isomeric SMILES: CCCCCCCC/C=CCCCCCCCCNCCCN
Molecular Formula: C21H44N2
DSSTOX Substance ID: DTXSID0027644

Molecular Weight: 324.6 g/mol
Physical Description: Liquid
CAS No.: 7173-62-8
CAS Registry Number: 7173-62-8
Unique Ingredient Identifier: 54XL96S8SY
Molecular Formula: C21H44N2
International Chemical Identifier (InChI): TUFJPPAQOXUHRI-KTKRTIGZSA-N
SMILES: C(=CCCCCCCCCNCCCN)CCCCCCCC
EINECS: 230-528-9
Properties:
Molecular Weight: 324.58746 g·mol−1

Density: 0.851 g/cm³
Boiling Point: 435.6 °C at 760 mmHg
Flash Point: 257.5 °C
Water Solubility: 36 mg/L at 23 °C
Vapor Pressure: 0.002 Pa at 20 °C
pKa: 10.67 ± 0.19 (Predicted)
Refractive Index: 1.464
Molecular Weight: 324.6 g/mol
XLogP3-AA: 7.1
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 19
Exact Mass: 324.350449412 g/mol

Monoisotopic Mass: 324.350449412 g/mol
Topological Polar Surface Area: 38 Å²
Heavy Atom Count: 23
Formal Charge: 0
Complexity: 226
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 1
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1

Compound Is Canonicalized: Yes
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Soluble in:
Water, 0.03723 mg/L @ 25 °C (est)
Chemical Formula: C21H44N2
Molar Mass: 324.597 g·mol−1
Appearance: Colourless or yellow liquid
Odor: Ammoniacal
Density: 0.841 g/cm³
Melting Point: 12 °C (54 °F; 285 K)
Boiling Point: 300 °C (572 °F; 573 K)

Solubility in Water: Insoluble (at 20 °C)
Solubility: Soluble in acetone, methanol
Product Name: N1-(9Z)-9-Octadecen-1-yl-1,3-propanediamine
CAS No.: 7173-62-8
UN No.: 2922
Molecular Formula: C21H44N2
InChIKeys: InChIKey=TUFJPPAQOXUHRI-KTKRTIGZSA-N
Molecular Weight: 324.58746
Exact Mass: 324.59
EC Number: 230-528-9
PSA: 38.05000

XLogP3: 7.05350
Density: 0.851 g/cm³
Boiling Point: 435.6 °C at 760 mmHg
Flash Point: 257.5 °C
Refractive Index: 1.464
Appearance: Light yellow to yellow liquid or slurry
Melting Point: 12 °C
Boiling Point: 435.6 °C
Density: 0.851
Solubility: N-Oleyl-1,3-propanediamine (7173-62-8) is insoluble in water.

FIRST AID MEASURES of OLEYL PROPYLENE DIAMINE:
-Description of first-aid measures:
*General advice:
Consult a physician.
*If inhaled:
If breathed in, move person into fresh air.
Consult a physician.
*In case of skin contact:
Wash off with soap and plenty of water.
Consult a physician.
*In case of eye contact:
Flush eyes with water as a precaution.
*If swallowed:
Rinse mouth with water.
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available

ACCIDENTAL RELEASE MEASURES of OLEYL PROPYLENE DIAMINE:
-Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.
-Methods and materials for containment and cleaning up:
Soak up with inert absorbent material.
Keep in suitable, closed containers for disposal.

FIRE FIGHTING MEASURES of OLEYL PROPYLENE DIAMINE:
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
-Further information:
No data available

EXPOSURE CONTROLS/PERSONAL PROTECTION of OLEYL PROPYLENE DIAMINE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
*Skin protection:
Handle with gloves.
Wash and dry hands.
*Body Protection:
Impervious clothing.
-Control of environmental exposure:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

HANDLING and STORAGE of OLEYL PROPYLENE DIAMINE:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.

STABILITY and REACTIVITY of OLEYL PROPYLENE DIAMINE:
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available