Page last updated: 2024-12-06

3-chloropropyltrimethoxysilane

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

3-Chloropropyltrimethoxysilane (CPTMS) is a bifunctional organosilane that contains both a chloropropyl group and a trimethoxysilyl group. It is a colorless liquid with a pungent odor and is widely used as a coupling agent, adhesion promoter, and cross-linking agent in various industrial applications.

CPTMS is typically synthesized via a reaction between trichlorosilane and allyl alcohol, followed by chlorination of the resulting allyltrichlorosilane to produce 3-chloropropyltrichlorosilane. The final product is then obtained through a reaction with methanol.

The chloropropyl group of CPTMS can react with hydroxyl groups on surfaces, while the trimethoxysilyl group can hydrolyze and condense with itself or other silanes to form siloxane bonds. This bifunctional nature makes CPTMS an effective coupling agent, promoting adhesion between different materials, such as glass, metal, and polymers.

CPTMS is extensively studied due to its versatile applications in various fields. For example, it is used as a silane coupling agent in the production of composite materials, sealants, and adhesives. Its ability to improve the adhesion of coatings to substrates has made it a valuable component in paints, varnishes, and resins. Additionally, CPTMS is utilized in the synthesis of functionalized silica nanoparticles, which have applications in drug delivery, catalysis, and sensors.

CPTMS can be toxic and irritant, and proper handling and safety precautions are essential when working with this chemical. Its environmental impact is also a subject of research, as it can potentially degrade into harmful byproducts. However, its wide-ranging applications and unique properties have made it a valuable compound in various industrial sectors.'

Cross-References

ID SourceID
PubMed CID62449
CHEMBL ID3184213
SCHEMBL ID37352
MeSH IDM0546027

Synonyms (70)

Synonym
cps-m
kbm 703
(gamma-chloropropyl)trimethoxysilane
3-(trimethoxysilyl)propyl chloride
sila-ace s 620
nsc 83878
3-chloropropyltrimethoxysilane
einecs 219-787-9
sh 6076
trimethoxy(3-chloropropyl)silane
gamma-chloropropyltrimethoxysilane ,
LS-13231
c6h15clo3si
AKOS008901063
(3-chloropropyl)trimethoxysilan
NCIOPEN2_001219
z 6076
a 143
2530-87-2
silane, (3-chloropropyl)trimethoxy-
silane (3-chloropropyl)tris(methoxy)-
.delta.-chloropropyltrimethoxysilane
nsc83878
(.gamma.-chloropropyl)trimethoxysilane
nsc-83878
.gamma.-chloropropyltrimethoxysilane
(3-chloropropyl)trimethoxysilane
3-chloropropyltrimethyoxysilane
(3-chloropropyl)trimethoxysilane, >=97%
(3-chloropropyl)(trimethoxy)silane
3-trimethoxysilylpropyl chloride
oxyzdrajmhgsmw-uhfffaoysa-
inchi=1/c6h15clo3si/c1-8-11(9-2,10-3)6-4-5-7/h4-6h2,1-3h3
3-chloropropyl-trimethoxysilane
3-chloropropyl trimethoxysilane
3-chloropropyl(trimethoxy)silane
NCGC00248491-01
NCGC00257567-01
cas-2530-87-2
tox21_200013
dtxcid207490
dtxsid4027490 ,
A817776
ec 219-787-9
unii-t21bnl1s7f
t21bnl1s7f ,
FT-0604706
S04675
SCHEMBL37352
cptmo
cl(ch2)3si(och3)3
(ch3o)3si(ch2)3cl
chloropropyltrimethoxy-silane
chloropropyltrimethoxysilane
3-trimethoxysilylpropylchloride
3-chloropropyltrimethoxy silane
trimethoxysilylpropyl chloride
chloropropyl trimethoxysilane
petrarch c3300
dow corning z-6076
dynasylan cptmo
trimethoxy-(3-chloropropyl) silane
c 3300
CHEMBL3184213
mfcd00000997
E77194
(3-chloro-propyl)-trimethoxy-silane
Q27289563
CS-0186811
163219-73-6
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (3)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
AR proteinHomo sapiens (human)Potency48.25420.000221.22318,912.5098AID743063
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency14.99280.000323.4451159.6830AID743065; AID743067
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency67.54470.000627.21521,122.0200AID743219
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (6)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's5 (83.33)24.3611
2020's1 (16.67)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 35.24

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index35.24 (24.57)
Research Supply Index1.95 (2.92)
Research Growth Index5.21 (4.65)
Search Engine Demand Index39.48 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (35.24)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other6 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]