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Siloxanes and Silicones, di-Me, 3-aminopropyl group-terminated
[CAS# 106214-84-0]

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Identification
ClassificationChemical reagent >> Organic reagent >> Siloxane
NameSiloxanes and Silicones, di-Me, 3-aminopropyl group-terminated
Synonyms3-[[[3-aminopropyl(dimethyl)silyl]oxy-dimethylsilyl]oxy-dimethylsilyl]propan-1-amine
Molecular StructureCAS # 106214-84-0, Siloxanes and Silicones, di-Me, 3-aminopropyl group-terminated
Molecular FormulaH2N(CH2)3Si(CH3)2O[Si(CH3)2O]nSi(CH3)2(CH2)3NH2
Molecular Weight~2500
CAS Registry Number106214-84-0
EC Number600-723-7
SMILESC[Si](C)(CCCN)O[Si](C)(C)O[Si](C)(C)CCCN
Properties
Density0.98 g/mL (25 °C) (Expl.)
Boiling point>200 °C (Expl.)
Refraction index1.410 (Expl.)
Safety Data
Hazard Symbolssymbol symbol symbol   GHS05;GHS07;GHS09 Danger  Details
Risk StatementsH315-H318-H319-H335-H400-H410  Details
Safety StatementsP261-P264-P264+P265-P271-P273-P280-P302+P352-P304+P340-P305+P351+P338-P305+P354+P338-P317-P319-P321-P332+P317-P337+P317-P362+P364-P391-P403+P233-P405-P501  Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Serious eye damageEye Dam.1H318
Specific target organ toxicity - single exposureSTOT SE3H335
Eye irritationEye Irrit.2H319
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Acute hazardous to the aquatic environmentAquatic Acute1H400
Skin corrosionSkin Corr.1BH314
Specific target organ toxicity - single exposureSTOT SE3H336
Skin corrosionSkin Corr.1CH314
Acute toxicityAcute Tox.4H312
Acute toxicityAcute Tox.4H302
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
SDSAvailable
up Discovery and Applications
Siloxanes and silicones, di-Me, 3-aminopropyl group-terminated, refer to a class of organosilicon compounds that consist of polydimethylsiloxane (PDMS) chains with terminal functional groups containing 3-aminopropyl substituents. These materials are a specific subset of amino-functional silicones and have been widely developed and applied in industrial, cosmetic, and biomedical fields due to their unique combination of silicone backbone properties and reactive amino terminal groups.

The core structure of these compounds is based on repeating –Si(CH3)2–O– units, forming a flexible, hydrophobic, and thermally stable siloxane polymer chain. The 3-aminopropyl groups are covalently bonded to the terminal silicon atoms of the polymer, introducing reactive primary amine functionalities. The presence of these amino groups allows for further chemical modification, crosslinking, or interaction with various substrates and surfaces.

These aminopropyl-terminated silicones were developed to expand the application range of silicone materials by introducing functionalities that enhance adhesion, reactivity, and compatibility with other materials. The terminal amino groups can participate in condensation reactions, epoxy or isocyanate curing, and hydrogen bonding, making them particularly valuable in applications requiring surface treatment, coupling, or adhesion to organic and inorganic materials.

In industrial use, these functional silicones serve as intermediates or additives in the formulation of adhesives, sealants, and coatings. They improve bonding performance to substrates such as glass, metal, and plastics, which would otherwise be difficult for conventional silicones to adhere to. They are also employed in sol-gel processes, resin modification, and surface functionalization.

In cosmetics and personal care products, low molecular weight variants of these aminopropyl-terminated silicones are utilized for their conditioning properties. They can deposit onto hair or skin and form flexible films that improve softness, smoothness, and manageability. The amino functionality can enhance substantivity to keratinous surfaces, leading to longer-lasting effects in rinse-off applications like shampoos and conditioners.

In biomedical and pharmaceutical fields, research has explored their use in drug delivery systems, medical adhesives, and tissue-compatible materials. Their flexibility, low toxicity, and biocompatibility make them suitable candidates for applications that require controlled surface interactions or long-term skin contact.

These compounds are typically clear to slightly yellowish fluids, with viscosities ranging from low (several hundred centistokes) to high depending on the degree of polymerization. They exhibit excellent thermal and oxidative stability and low surface energy, while the amino terminal groups introduce hydrophilic and reactive characteristics to an otherwise inert silicone backbone.

Safety evaluations have shown that these materials are generally considered safe in formulated products when used appropriately. The reactivity of the amino groups may pose irritation risks if used at high concentrations or in uncontrolled applications. Proper formulation and end-use testing are important to ensure product performance and safety.

In summary, siloxanes and silicones, di-Me, 3-aminopropyl group-terminated, are functionalized silicone polymers with terminal primary amino groups that enhance their reactivity and surface interaction properties. Their unique combination of silicone flexibility and amine functionality enables widespread use in industrial, cosmetic, and emerging biomedical applications.

References

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