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Methylmalondialdehyde is a chemical compound derived from malondialdehyde, a highly reactive and potentially harmful molecule that is a byproduct of lipid peroxidation. It is formed during the breakdown of certain fatty acids and is known for its ability to cause damage to cellular proteins and DNA. Methylmalondialdehyde has been linked to various pathological conditions, including cardiovascular disease and neurological disorders. It is considered a marker of oxidative stress and is often used as a biomarker for identifying and quantifying oxidative damage in biological systems. The presence of methylmalondialdehyde in the body is thought to be indicative of increased oxidative stress and may serve as a useful indicator of disease risk and progression.

16002-19-0

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16002-19-0 Usage

Uses

Used in Medical Research:
Methylmalondialdehyde is used as a biomarker for oxidative stress in various pathological conditions, including cardiovascular disease and neurological disorders. Its presence in the body is indicative of increased oxidative stress and may serve as a useful indicator of disease risk and progression.
Used in Diagnostics:
Methylmalondialdehyde is used as a diagnostic tool to identify and quantify oxidative damage in biological systems. Its measurement can help assess the extent of oxidative stress and monitor the effectiveness of treatments aimed at reducing oxidative stress.
Used in Pharmaceutical Development:
Methylmalondialdehyde may be used in the development of pharmaceuticals targeting oxidative stress-related conditions. Understanding its role in disease development can aid in the design of drugs that modulate its production or mitigate its harmful effects.
Used in Nutritional Research:
Methylmalondialdehyde can be used in nutritional research to study the effects of diet and supplements on oxidative stress levels. Identifying dietary factors that influence methylmalondialdehyde levels can help develop recommendations for reducing oxidative stress and promoting overall health.
Used in Environmental Studies:
Methylmalondialdehyde can be used as a biomarker to assess the impact of environmental factors, such as pollution or radiation, on oxidative stress levels in living organisms. This can help evaluate the potential health risks associated with exposure to these factors and inform public health policies.

Check Digit Verification of cas no

The CAS Registry Mumber 16002-19-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,0 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16002-19:
(7*1)+(6*6)+(5*0)+(4*0)+(3*2)+(2*1)+(1*9)=60
60 % 10 = 0
So 16002-19-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H6O2/c1-4(2-5)3-6/h2-4H,1H3

16002-19-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylpropanedial

1.2 Other means of identification

Product number -
Other names Propanedial,2-methyl

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:16002-19-0 SDS

16002-19-0Relevant academic research and scientific papers

Anti-platelet drug AZD6482 method for the preparation of

-

Paragraph 0020; 0036-0037, (2020/02/08)

The invention discloses a preparation method for an antiplatelet medicine AZD6482 (I). The preparation method comprises the following preparation steps: preparing from common chemical raw materials such as propionaldehyde and acetoacetamide to obtain an i

New nucleoside analogues for the recognition of pyrimidine-purine inversion sites

Buchini, Sabrina,Leumann, Christian J.

, p. 1199 - 1201 (2007/10/03)

A new nucleoside designed to enhance triplex stability has been synthesised in 15 steps starting from sugar 2. This pathway contains the sugar derivative 9 which is a useful intermediate for the introduction of other natural and unnatural bases into the 2′-aminoethoxy nucleoside containing scaffold.

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