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26100-51-6

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26100-51-6 Usage

Description

Polylactic acid (PLA) is a biodegradable and bioresorbable polymer derived from the cyclic diester of lactic acid (lactide) through ring-opening addition polymerization. It is composed of repeating 2-hydroxypropanoyl units, making it a macromolecule with excellent surface quality and light weight properties.

Uses

Used in Surgical Implants:
Polylactic acid is used as a degradable surgical implant material, introduced in 1966. It undergoes hydrolysis to yield lactic acid, a normal intermediate of carbohydrate metabolism, which coincides with the healing sequence of natural tissues. The bioresorbability and hydrolytic resistance of PLA depend on its purity and processing conditions.
Used in Drug Delivery Systems:
Poly(L-lactide) (PLLA) is a semi-crystalline biodegradable polymer used in drug delivery applications. Its acetylene functionality is commonly utilized in copper-mediated ligation, making it a versatile material for controlled drug release systems.
Used in 3D Printing Filaments:
CarbonX? CFR-PLA is an improved carbon fiber reinforced 3D printing filament made using premium Natureworks PLA and high modulus carbon fiber. It is ideal for structural components with high modulus, excellent surface quality, light weight, and ease of printing.
Used as a Filler:
Polylactic acid can also be used as a filler material in various applications due to its properties.
Solubility:
PLLA is soluble in toluene, THF, CHCl3, and CH2Cl2, but insoluble in methanol, hexane, and ether.

Check Digit Verification of cas no

The CAS Registry Mumber 26100-51-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,0 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26100-51:
(7*2)+(6*6)+(5*1)+(4*0)+(3*0)+(2*5)+(1*1)=66
66 % 10 = 6
So 26100-51-6 is a valid CAS Registry Number.
InChI:InChI=1/C3H6O3/c1-2(4)3(5)6/h2,4H,1H3,(H,5,6)

26100-51-6 Well-known Company Product Price

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  • Aldrich

  • (38534)  Polylacticacid  Mw ~60,000

  • 26100-51-6

  • 38534-1G

  • 1,327.95CNY

  • Detail
  • Aldrich

  • (38534)  Polylacticacid  Mw ~60,000

  • 26100-51-6

  • 38534-5G

  • 4,571.19CNY

  • Detail

26100-51-6SDS

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 poly(lactic acid) macromolecule

1.2 Other means of identification

Product number -
Other names Poly(2-hydroxypropionic 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:26100-51-6 SDS

26100-51-6Relevant articles and documents

Photothermal strategy for the highly efficient conversion of glucose into lactic acid at low temperatures over a hybrid multifunctional multi-walled carbon nanotube/layered double hydroxide catalyst

Duo, Jia,Jin, Binbin,Jin, Fangming,Shi, Xiaoyu,Wang, Tianfu,Ye, Xin,Zhong, Heng

, p. 813 - 822 (2022/02/09)

The conversion of carbohydrates into lactic acid has attracted increasing attention owing to the broad applications of lactic acid. However, the current methods of thermochemical conversion commonly suffer from limited selectivity or the need for harsh conditions. Herein, a light-driven system of highly selective conversion of glucose into lactic acid at low temperatures was developed. By constructing a hybrid multifunctional multi-walled carbon nanotube/layered double hydroxide composite catalyst (CNT/LDHs), the highest lactic acid yield of 88.6% with 90.0% selectivity was achieved. The performance of CNT/LDHs for lactic acid production from glucose is attributed to the following factors: (i) CNTs generate a strong heating center under irradiation, providing heat for converting glucose into lactic acid; (ii) LDHs catalyze glucose isomerization, in which the photoinduced OVs (Lewis acid) in LDHs under irradiation further improve the catalytic activity; and (iii) in a heterogeneous-homogeneous synergistically catalytic system (LDHs-OH-), OH- ions are concentrated in LDHs, forming strong base sites to catalyze subsequent cascade reactions.

Ce promoted Cu/γ-Al2O3 catalysts for the enhanced selectivity of 1,2-propanediol from catalytic hydrogenolysis of glucose

Balachandran Kirali, Arun Arunima,Marimuthu, Banu,Sreekantan, Sreejith

, (2022/03/31)

Ce promoted Cu/γ-Al2O3 catalysts were prepared with varying amounts of Cu (x = 0–10 wt%) and Ce (y = 0–15 wt%). The prepared catalysts were characterized and tested for the conversion of aqueous glucose (5 wt%) to 1,2-propanediol in a batch reactor. 10%Ce-8%Cu/γ-Al2O3 showed the complete conversion of glucose with 62.7% selectivity of 1,2-propanediol and total glycols (1,2-propanediol, ethylene glycol & 1,2-butanediol) of 81% at milder reaction conditions. Cu facilitated the hydrogenation activity and Ce loading optimize the acid/base sites of Cu/γ-Al2O3 which obtain high selectivity of 1, 2-propanediol. Catalyst reusability is reported.

Tin, molybdenum and tin-molybdenum oxides: Influence of Lewis and Bronsted acid sites on xylose conversion

Meneghetti, Mario R.,Meneghetti, Simoni M. P.,Pryston, Dhara B. A.,da Silva Avelino, Débora Olimpio,dos Santos, Thatiane V.

, (2021/11/16)

In this study, tin oxide (SnO2), molybdenum oxide (MoO3) and a mixed oxide based on tin and molybdenum (respectively, Sn100, Mo100 and SnMo25, synthesized by the impregnation method) were applied in xylose conversion. The best results were obtained employing Mo100 and SnMo25. In the presence of SnMo25, after 0.5 h, xylose conversions of 39.5%, 34.1% and 63.4% were obtained, respectively, at 110, 130 and 150 °C. For Mo100, conversions of 49.6%, 71.8% and 85.3% were attained under the same reaction conditions, showing that Mo100 provided the best conversion results. However, with the use of this catalyst there was an increase in the amount of soluble and insoluble polymeric material. In terms of the soluble products formed from xylose, depending on the reaction condition were detected xylulose (X), lyxose (L) and furfural (FUR), glyceraldehyde (GL), pyruvaldehyde (PYR), glycoaldehyde (GLYC), dihydroxyacetone (DHA), lactic acid (AL), levulinic acid (LA) and acetic acid (AA). However, with the use of Sn100 or without a catalyst (systems with low conversions) there was mainly the formation of lyxose. The use of Mo100 and SnMo25 (systems which exhibit high acidity) leads mainly to isomerization, epimerization and dehydration reactions, as in the case of the retro-aldol pathway and furfural conversion, highlighting the importance of Lewis and Bronsted acid sites in relation to modulating the selectivity of the systems.

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