3001-64-7

Basic information

• Product Name: 2-mercaptopropanol
• Synonyms: 2-mercaptopropanol;2-Mercapto-1-propanol;Einecs 221-084-7
• CAS NO: 3001-64-7
• Molecular Formula: C₃H₈OS
• Molecular Weight: 92.16002
• EINECS: 221-084-7
• Mol File: 3001-64-7.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 158.3°Cat760mmHg
• Flash Point: 49.6°C
• Appearance: /
• Density: 1.024g/cm³
• Vapor Pressure: 0.938mmHg at 25°C
• Refractive Index: 1.475
• PKA: 10.08±0.10(Predicted)
• CAS DataBase Reference: 2-mercaptopropanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-mercaptopropanol(3001-64-7)
• EPA Substance Registry System: 2-mercaptopropanol(3001-64-7)

Safety Data

• Hazardous Substances Data: 3001-64-7(Hazardous Substances Data)

Usage

General Description

2-mercaptopropanol, also known as 2-MP, is a chemical compound with the molecular formula C3H8OS. It is a colorless liquid with a strong, unpleasant odor, and is commonly used as a solvent, as well as in the production of pharmaceuticals and organic compounds. 2-MP is also used in the manufacturing of cosmetics and personal care products, due to its ability to act as a fragrance and skin conditioning agent. It is also utilized as an intermediate in the synthesis of various chemicals, such as agrochemicals and rubber chemicals. Additionally, 2-mercaptopropanol is used in the production of metal salts, which are then used in the manufacturing of catalysts and pigments. Overall, 2-MP has a wide range of applications in various industries due to its versatile properties and functions.

InChI:InChI=1/C3H8OS/c1-3(5)2-4/h3-5H,2H2,1H3

Upstream product

• 73232-07-2 2-ethoxythiocarbonyl sulfanyl-propionic acid ethyl ester 
• 79-42-5 2-mercaptopropanoic acid 
• 53907-46-3 methyl 2-mercaptopropionate 
• 6405-82-9 acetyl-chloro-sulfane 
• 292638-85-8 acrylic acid methyl ester 
• 107-19-7 propargyl alcohol 

Downstream Products

• 20463-93-8 2-(methylthio)-2-methylethanol 
• 1072-43-1 propylene sulphide 
• 72311-96-7 2-ethylthio-2-propanol 
• 32300-62-2 2-(2,4-dinitro-phenylsulfanyl)-propan-1-ol 

Relevant articles and documents

PBD CONJUGATES FOR TREATING DISEASES

The present disclosure relates to pyrrolobenzodiazepine (PBD) prodrugs and conjugates thereof. The present disclosure also relates to pharmaceutical compositions of the conjugates described herein, methods of making and methods of using the same.

1-(CHLOROMETHYL)-2,3-DIHYDRO-1H-BENZO[E]INDOLE DIMER ANTIBODY-DRUG CONJUGATE COMPOUNDS, AND METHODS OF USE AND TREATMENT

The invention provides antibody-drug conjugates comprising an antibody conjugated to a 1-(chloromethyl)-2,3-dihydro-1H-benzo[e]indole (CBI) dimer drug moiety via a linker, and methods of using the antibody-drug conjugates.

Synthesis and Insecticidal Activity of Oxazaphospholidines, Oxathiaphospholanes, and Thiazaphospholidines

Fifty-five new five-membered cyclic organophosphorus compounds including oazaphospholidines, thiazaphospholidines, and oxathiaphospholanes were synthesized, which have substituents at 4- or/and 5-positions besides at the 2-position.The thiazaphospholidines showed the highest insecticidal activity followed by oxathiaphospholanes and oxazaphospholidines.The position preference of substituents in insecticidal activity was most obvious in the oxazaphospholidines.It was preferable for insecticidal activity to have the substituent near the more basic atom: the 4-position for thiazaphospholidine and oxazaphospholidine, the 5-position for oxathiaphospholane, with the exception of 4- or 5-phenyl oxazaphospholidine.