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CAS

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100048-86-0

2-(Bromomethyl)-2-butylhexanoic acid is a synthetic chemical compound with the molecular formula C11H21BrO2. It is a derivative of butylated hydroxytoluene, known for its antioxidant properties in food and cosmetic products. The presence of the bromomethyl group in its structure endows it with reactivity, allowing it to form covalent bonds with other molecules, which is crucial for the synthesis of a variety of organic compounds. 2-(Bromomethyl)-2-butylhexanoic acid also serves as a precursor in pharmaceutical production and as a building block for complex organic molecules in chemical reactions. Furthermore, it has been investigated for its potential biological activity and therapeutic efficacy in various diseases.

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  • 100048-86-0 Structure

  • Basic information

    1. Product Name: 2-(Bromomethyl)-2-butylhexanoic acid
    2. Synonyms: 2-(Bromomethyl)-2-butylhexanoic acid;2-Bromomethyl-2-n-butyl hexanoic acid
    3. CAS NO:100048-86-0
    4. Molecular Formula: C11H21BrO2
    5. Molecular Weight: 265.18724
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100048-86-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 41 °C
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.216
    6. Refractive Index: N/A
    7. Storage Temp.: Inert atmosphere,Room Temperature
    8. Solubility: N/A
    9. PKA: 4.05±0.50(Predicted)
    10. CAS DataBase Reference: 2-(Bromomethyl)-2-butylhexanoic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(Bromomethyl)-2-butylhexanoic acid(100048-86-0)
    12. EPA Substance Registry System: 2-(Bromomethyl)-2-butylhexanoic acid(100048-86-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 100048-86-0(Hazardous Substances Data)

100048-86-0 Usage

Uses

Used in Pharmaceutical Production:
2-(Bromomethyl)-2-butylhexanoic acid is used as a precursor in the synthesis of pharmaceuticals for its ability to form covalent bonds with other molecules, contributing to the development of new drugs.
Used in Organic Chemical Reactions:
In the field of organic chemistry, 2-(Bromomethyl)-2-butylhexanoic acid is utilized as a building block for constructing complex organic molecules, thanks to its reactive bromomethyl group that facilitates the formation of new chemical bonds.
Used in Antioxidant Applications:
As a derivative of butylated hydroxytoluene, 2-(Bromomethyl)-2-butylhexanoic acid is used in food and cosmetic products as an antioxidant to prevent oxidation and extend the shelf life of these products.
Used in Research and Development:
2-(Bromomethyl)-2-butylhexanoic acid is also used in research settings to study its potential biological activity and explore its therapeutic potential in treating various diseases, making it a valuable tool in the advancement of medical science.

Check Digit Verification of cas no

The CAS Registry Mumber 100048-86-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,0,4 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 100048-86:
(8*1)+(7*0)+(6*0)+(5*0)+(4*4)+(3*8)+(2*8)+(1*6)=70
70 % 10 = 0
So 100048-86-0 is a valid CAS Registry Number.

100048-86-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Bromomethyl)-2-butylhexanoic acid

1.2 Other means of identification

Product number -
Other names 2-(bromomethyl)-2-butyl-hexanoic 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:100048-86-0 SDS

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100048-86-0Relevant articles and documents

Novel 1,4-benzothiazephine and 1,5-benzothiazepine compounds as inhibitors of apical sodium co-dependent bile acid transport and taurocholate uptake

-

, (2008/06/13)

Compounds, pharmaceutical compositions, and methods for the treatment of a hyperlipidemic condition in a subject. The compounds of the present invention are apical sodium co-dependent bile acid transport inhibitors and are 1,4-benzothiazepine and 1,5-benzothiazepine compounds corresponding to Formula I: wherein j, m, Y, Z, R1A, R1B, R2A, R2B and R6 are as defined in the specification.

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