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Merck
CN

C68601

3-Chloro-1-propanethiol

98%

Synonym(s):

γ-Chloropropyl mercaptan, 3-Chloropropan-1-thiol, 3-Chloropropanethiol, 3-Chloropropyl mercaptan

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About This Item

Linear Formula:
Cl(CH2)3SH
CAS Number:
Molecular Weight:
110.61
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
241-496-0
MDL number:
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Product Name

3-Chloro-1-propanethiol, 98%

InChI key

TZCFWOHAWRIQGF-UHFFFAOYSA-N

InChI

1S/C3H7ClS/c4-2-1-3-5/h5H,1-3H2

SMILES string

SCCCCl

assay

98%

form

liquid

refractive index

n20/D 1.4921 (lit.)

bp

145.5 °C (lit.)

density

1.136 g/mL at 25 °C (lit.)

Quality Level

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Application

  • Solution-Phase Hybrid Passivation: 3-Chloro-1-propanethiolis used in the passivation of quantum dots to enhance the performance of infrared-band gap quantum dot solar cells, suggesting significant improvements in efficiency and stability (Mahajan et al., 2020).

General description

3-Chloro-1-propanethiol is a sulfur-containingcompound used as a building block in organic synthesis.It acts as a nucleophilic reagent in SN2 reactions. .

pictograms

FlameExclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

109.4 °F - closed cup

flash_point_c

43 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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The Staudinger reaction with 2-imino-1, 3-thiaselenanes toward the synthesis of C4 spiro-$\beta$-lactams
Toyoda, Yosuke and Ninomiya, et al.
Organic & Biomolecular Chemistry, 11, 2652-2659 (2013)
New ultrastable mesoporous adsorbent for the removal of mercury ions
De Canck, Els and Lapeire, et al.
Langmuir, 26, 10076-10083 (2010)
Arxel de León et al.
Journal of colloid and interface science, 456, 182-189 (2015-07-01)
The incorporation of gold nanoparticles in heterojunction solar cells is expected to increase the efficiency due to plasmon effects, but the literature studies are sometimes controversial. In this work, gold nanoparticles passivated with (Ph)n-(CH2)3SH (n=1, 2, 3) have been synthesized

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