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7-CARBOXY-1-HEPTANETHIOL, also known as 8-Mercaptooctanoic acid (MOA), is a carboxylic acid-terminated alkanethiol that forms self-assembled monolayers (SAMs) on surfaces. These monolayers facilitate the immobilization of other molecular species, making it a versatile compound for various applications in different industries.

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  • 74328-61-3 Structure
  • Basic information

    1. Product Name: 7-CARBOXY-1-HEPTANETHIOL
    2. Synonyms: 7-CARBOXY-1-HEPTANETHIOL;8-Mercaptooctanoic acid,8-Thiooctanoic acid, MOA;MOA;8-Mercaptooctanoic acid 95%;8-sulfanyloctanoic acid
    3. CAS NO:74328-61-3
    4. Molecular Formula: C8H16O2S
    5. Molecular Weight: 176.27644
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 74328-61-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 302 °C at 760 mmHg
    3. Flash Point: 136.4 °C
    4. Appearance: /
    5. Density: 1.0326 g/mL at 25 °C
    6. Vapor Pressure: 0.000237mmHg at 25°C
    7. Refractive Index: n20/D 1.4808
    8. Storage Temp.: ?20°C
    9. Solubility: N/A
    10. PKA: 4.77±0.10(Predicted)
    11. CAS DataBase Reference: 7-CARBOXY-1-HEPTANETHIOL(CAS DataBase Reference)
    12. NIST Chemistry Reference: 7-CARBOXY-1-HEPTANETHIOL(74328-61-3)
    13. EPA Substance Registry System: 7-CARBOXY-1-HEPTANETHIOL(74328-61-3)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26
    4. RIDADR: UN 3334
    5. WGK Germany: 3
    6. RTECS:
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 74328-61-3(Hazardous Substances Data)

74328-61-3 Usage

Uses

Used in Surface Modification:
7-CARBOXY-1-HEPTANETHIOL is used as a self-assembled monolayer (SAM) for surface modification of gold electrodes. This modification is crucial for various applications, such as quartz crystal microbalance (QCMB) measurements.
Used in Biomedical Applications:
In the biomedical industry, 7-CARBOXY-1-HEPTANETHIOL is used as a monolayer that facilitates ferritin absorption on gold electrodes. This application aids in the uptake of excess iron in cells, which can be beneficial for certain medical treatments or diagnostics.
Used in Photothermal Therapy:
7-CARBOXY-1-HEPTANETHIOL is also used in the preparation of nitric oxide-based gold nanoparticles (NO-AuNPs) for macrophage photo-thermal therapy under near-infrared (NIR) irradiation. This application is particularly relevant in the field of cancer treatment, where localized heating can be used to target and destroy cancer cells.

Check Digit Verification of cas no

The CAS Registry Mumber 74328-61-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,3,2 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 74328-61:
(7*7)+(6*4)+(5*3)+(4*2)+(3*8)+(2*6)+(1*1)=133
133 % 10 = 3
So 74328-61-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O2S/c9-8(10)6-4-2-1-3-5-7-11/h11H,1-7H2,(H,9,10)

74328-61-3 Well-known Company Product Price

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  • Aldrich

  • (675075)  8-Mercaptooctanoicacid  95%

  • 74328-61-3

  • 675075-1G

  • 2,054.52CNY

  • Detail

74328-61-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-sulfanyloctanoic acid

1.2 Other means of identification

Product number -
Other names 8-Mercaptooctanoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:74328-61-3 SDS

74328-61-3Upstream product

74328-61-3Relevant articles and documents

Derivatized virginiamycin M1

-

, (2008/06/13)

Derivatized type A virginiamycins having a reactive functionalized side chain, and a process for making the virginiamycin derivatives. The side chain contains a thioether linkage and a reactive group, such as a carboxylate ester or free carboxylic acid group.

Azole derivatives

-

, (2008/06/13)

Azole derivatives of the formula SPC1 Wherein R1 is free or esterified carboxyl or other functionally modified carboxyl group, R2 and R3 each are aryl; A is Cn H2n in which n is an integer from 1 to 10, inclusive; and Z is O or S; and the physiologically acceptable salts thereof, possess, with good compatibility, excellent antiphlogistic activity and, in particular, influence favorably the chronic progressive diseases of the joints, e.g., arthritis. They can be prepared from compounds of the formula SPC2 Wherein X1 is a group convertible into the group --S--A--R1, and R2 and R3 have the values given above.

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