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29435-48-1

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29435-48-1 Usage

Description

BIOPOL is a biodegradable and biocompatible polymer known as Poly[(R)-3-hydroxybutyric acid (PHB)], which is produced by several bacterial species. It is characterized by its low resorbability and tunable properties, making it a versatile material for various applications.

Uses

Used in Tissue Engineering:
BIOPOL is used as a scaffold material for tissue engineering due to its biocompatibility and biodegradability, which support cell growth and tissue regeneration.
Used in Controlled Release Systems:
BIOPOL is used as a matrix material for controlled release systems in the pharmaceutical industry, allowing for the sustained and targeted delivery of drugs.
Used in Packaging Industry:
BIOPOL is used as an eco-friendly alternative to traditional plastics for packaging materials, reducing environmental impact and promoting sustainability.
Used in Medical Devices:
BIOPOL is used as a component in the manufacturing of medical devices, such as sutures and implants, due to its biocompatibility and ability to degrade within the body without causing adverse reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 29435-48-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,4,3 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 29435-48:
(7*2)+(6*9)+(5*4)+(4*3)+(3*5)+(2*4)+(1*8)=131
131 % 10 = 1
So 29435-48-1 is a valid CAS Registry Number.

29435-48-1 Well-known Company Product Price

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  • Aldrich

  • (363502)  Poly[(R)-3-hydroxybutyricacid]  natural origin

  • 29435-48-1

  • 363502-10G

  • 1,377.09CNY

  • Detail
  • Aldrich

  • (363502)  Poly[(R)-3-hydroxybutyricacid]  natural origin

  • 29435-48-1

  • 363502-100G

  • 8,154.90CNY

  • Detail

29435-48-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-oxo-4-(4-oxobutan-2-yloxy)butan-2-yl] 3-hydroxybutanoate

1.2 Other means of identification

Product number -
Other names Poly[(R)-3-hydroxybutyric 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:29435-48-1 SDS

29435-48-1Relevant articles and documents

SYNTHESIS OF 3-HYDROXYBUTYRYL 3-HYDROXYBUTYRATE AND RELATED COMPOUNDS

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Paragraph 0308; 0320-0324, (2021/04/02)

In various embodiments methods of preparing hydroxybutyryl 3-hydroxybutyrate and related compounds are provided along with methods of use thereof.

Three new bioactive natural products from the fungus Talaromyces assiutensis JTY2

Cai, Jin,Chen, Guang-Ying,Liao, Qi-Ying,Liao, Shan,Meng, Bo-Zhen,Tang, Min-Min,Yang, Xing,Zhou, Xue-Ming

, (2019/12/24)

A novel cyclopentenone derivative, talarocyclopenta A (1), a new phenolicethers derivative, talarocyclopenta B (2) and a new itaconic acid derivative, talarocyclopenta C (3) together with four known itaconic acid derivatives (4–7) were isolated from the Talaromyces assiutensis JTY2. Their structures were elucidated by the detailed analysis of comprehensive spectroscopic data. Among them, talarocyclopent (1) is the first represent an unusual type of cyclopentenone derivative, possessing a cyclopentenone unit, a 2-butanone unit and a 3-hydroxybutyric acid unit. All isolated compounds were evaluated for their anti-inflammatory and antibacterial activities. Compounds 1–4 showed inhibitory activities against the nitric oxide (NO) production induced by lipopolysaccharide in mouse macrophage RAW 264.7 cells in vitro. Compound 2 showed broad spectrum antibacterial against six terrestrial pathogenic bacteria.

Synthesis of α,β- and β-Unsaturated Acids and Hydroxy Acids by Tandem Oxidation, Epoxidation, and Hydrolysis/Hydrogenation of Bioethanol Derivatives

Faria, Jimmy,Komarneni, Mallik R.,Li, Gengnan,Pham, Tu,Resasco, Daniel E.,Ruiz, Maria P.,Santhanaraj, Daniel

supporting information, p. 7456 - 7460 (2020/03/23)

We report a reaction platform for the synthesis of three different high-value specialty chemical building blocks starting from bio-ethanol, which might have an important impact in the implementation of biorefineries. First, oxidative dehydrogenation of ethanol to acetaldehyde generates an aldehyde-containing stream active for the production of C4 aldehydes via base-catalyzed aldol-condensation. Then, the resulting C4 adduct is selectively converted into crotonic acid via catalytic aerobic oxidation (62 % yield). Using a sequential epoxidation and hydrogenation of crotonic acid leads to 29 % yield of β-hydroxy acid (3-hydroxybutanoic acid). By controlling the pH of the reaction media, it is possible to hydrolyze the oxirane moiety leading to 21 % yield of α,β-dihydroxy acid (2,3-dihydroxybutanoic acid). Crotonic acid, 3-hydroxybutanoic acid, and 2,3-dihydroxybutanoic acid are archetypal specialty chemicals used in the synthesis of polyvinyl-co-unsaturated acids resins, pharmaceutics, and bio-degradable/ -compatible polymers, respectively.

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