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352431-47-1

3-METHYLBUTYRALDEHYDE-2,2-D2, with the CAS number 352431-47-1, is an isotopically labeled research compound that is utilized in various scientific studies and experiments. It is a deuterated version of 3-methylbutyraldehyde, which means it contains deuterium atoms instead of regular hydrogen atoms. This characteristic makes it valuable for research purposes, particularly in the field of chemistry and biochemistry.
Usage:
Used in Research and Development:
3-METHYLBUTYRALDEHYDE-2,2-D2 is used as a research compound for its isotopically labeled properties, which allow for the study of chemical reactions and processes with enhanced precision and control. The deuterium labeling can help in understanding reaction mechanisms, identifying reaction intermediates, and determining the position of hydrogen atoms in complex molecules.
Used in Chemical Synthesis:
In the field of chemical synthesis, 3-METHYLBUTYRALDEHYDE-2,2-D2 can be employed as a starting material or an intermediate for the synthesis of various deuterated organic compounds. The deuterium atoms in the compound can provide unique properties and advantages, such as increased stability or altered reactivity, which can be beneficial for specific applications.
Used in Analytical Chemistry:
3-METHYLBUTYRALDEHYDE-2,2-D2 can be utilized in analytical chemistry as a reference material or an internal standard for the quantification and identification of related compounds. The deuterium labeling can improve the accuracy and reliability of analytical techniques, such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy, by providing a distinct and easily distinguishable signal.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3-METHYLBUTYRALDEHYDE-2,2-D2 can be used as a tool for studying the metabolism and pharmacokinetics of drugs containing similar structures. The deuterium labeling can help in understanding the fate of the drug in the body, its distribution, and its potential interactions with other molecules, which can be crucial for drug design and optimization.
Used in Environmental Studies:
3-METHYLBUTYRALDEHYDE-2,2-D2 can also be employed in environmental research to study the behavior and fate of similar compounds in the environment. The deuterium labeling can provide insights into the transport, degradation, and bioaccumulation of these compounds, which can be essential for assessing their environmental impact and developing strategies for their management.

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  • 352431-47-1 Structure

  • Basic information

    1. Product Name: 3-METHYLBUTYRALDEHYDE-2,2-D2
    2. Synonyms: 3-METHYLBUTYRALDEHYDE-2,2-D2;3-Methylbutanal(2,2-D2);Isovaleraldehyde(2,2-D2);3-Methylbutyraldehyde--d2
    3. CAS NO:352431-47-1
    4. Molecular Formula: C5H8D2O
    5. Molecular Weight: 88.14
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 352431-47-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 93.5°Cat760mmHg
    3. Flash Point: °C
    4. Appearance: /
    5. Density: 0.81g/cm3
    6. Vapor Pressure: 49.3mmHg at 25°C
    7. Refractive Index: 1.382
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-METHYLBUTYRALDEHYDE-2,2-D2(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-METHYLBUTYRALDEHYDE-2,2-D2(352431-47-1)
    12. EPA Substance Registry System: 3-METHYLBUTYRALDEHYDE-2,2-D2(352431-47-1)

  • Safety Data

    1. Hazard Codes: F
    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: 352431-47-1(Hazardous Substances Data)

352431-47-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 352431-47-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,4,3 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 352431-47:
(8*3)+(7*5)+(6*2)+(5*4)+(4*3)+(3*1)+(2*4)+(1*7)=121
121 % 10 = 1
So 352431-47-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H10O/c1-5(2)3-4-6/h4-5H,3H2,1-2H3/i3D2

352431-47-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dideuterio-3-methylbutanal

1.2 Other means of identification

Product number -
Other names BIM0590

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:352431-47-1 SDS

352431-47-1Downstream Products

352431-47-1Relevant articles and documents

DEUTERATED ANALOGS OF ACETYL-LEUCINE

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Paragraph 0530; 0532, (2020/07/05)

The present disclosure provides compounds represented by Formula I: I, and the pharmaceutically acceptable salts and solvates thereof, wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11, R12, and R13 are as defined as set forth in the specification, and the deuterium enrichment of any one or more of R3, R4, R5, R6, R7, R8, R9, R10, R11, R12, and R13 is about 15% or more. The present disclosure also provides compounds having Formula I for use to treat or delay the progression of a lysosomal storage disorder or a neurodegenerative disease in a subject, provide neuroprotection in a subject having a lysosomal disorder, treat or prevent a migraine, and the symptoms associated therewith, in a subject, or improve mobility and/or cognitive function in a subject.

Boric acid compound, borate compound and their preparation methods and application

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Paragraph 0188; 0189, (2018/12/02)

The invention provides a boric acid compound and a borate compound shown as formula I and formula II which are shown in the description, and their preparation methods, application and pharmaceutical compositions. The boric acid compound and the borate compound can inhibit proteasome and are suitable for treating multiple myeloma.

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