天堂网亚洲,天天操天天搞,91视频高清,菠萝蜜视频在线观看入口,美女视频性感美女视频,95丝袜美女视频国产,超高清美女视频图片

Home Cart 0 Sign in  

[ CAS No. 13076-17-0 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 13076-17-0
Chemical Structure| 13076-17-0
Structure of 13076-17-0 * Storage: {[proInfo.prStorage]}

Please Login or Create an Account to: See VIP prices and availability

Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Search after Editing

* Storage: {[proInfo.prStorage]}

* Shipping: {[proInfo.prShipping]}

Quality Control of [ 13076-17-0 ]

Related Doc. of [ 13076-17-0 ]

Alternatived Products of [ 13076-17-0 ]
Product Citations

Product Citations

Bruna L. C. Cunha ; Juliana O. Bahú ; Letícia F. Xavier , et al. DOI: PubMed ID:

Abstract: Lactide dimer is an important monomer produced from lactic acid dehydration, followed by the prepolymer depolymerization process, and subsequent purification. As lactic acid is a chiral molecule, lactide can exist in three isomeric forms: L-, D-, and meso-lactide. Due to its time-consuming synthesis and the need for strict temperature and pressure control, catalyst use, low selectivity, high energy cost, and racemization, the value of a high purity lactide has a high cost in the market; moreover, little is found in scientific articles about the monomer synthesis. Lactide use is mainly for the synthesis of high molar mass poly(lactic acid) (PLA), applied as bio-based material for medical applications (e.g., prostheses and membranes), drug delivery, and hydrogels, or combined with other polymers for applications in packaging. This review elucidates the configurations and conditions of syntheses mapped for lactide production, the main properties of each of the isomeric forms, its industrial production, as well as the main applications in the market.

Keywords: applications ; industrial processes ; l-lactide ; market costs ; synthesis

Purchased from AmBeed:

Product Details of [ 13076-17-0 ]

CAS No. :13076-17-0 MDL No. :MFCD00082566
Formula : C6H8O4 Boiling Point : -
Linear Structure Formula :(OCH(CH3)CO)2 InChI Key :JJTUDXZGHPGLLC-QWWZWVQMSA-N
M.W : 144.13 Pubchem ID :5325924
Synonyms :

Calculated chemistry of [ 13076-17-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.67
Num. rotatable bonds : 0
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 31.41
TPSA : 52.6 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.72 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.21
Log Po/w (XLOGP3) : 0.64
Log Po/w (WLOGP) : -0.14
Log Po/w (MLOGP) : -0.15
Log Po/w (SILICOS-IT) : 0.7
Consensus Log Po/w : 0.45

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.14
Solubility : 10.5 mg/ml ; 0.073 mol/l
Class : Very soluble
Log S (Ali) : -1.32
Solubility : 6.9 mg/ml ; 0.0479 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.54
Solubility : 41.8 mg/ml ; 0.29 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.68

Safety of [ 13076-17-0 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:
Recommend Products
Same Skeleton Products

Technical Information

Historical Records

Similar Product of
[ 13076-17-0 ]

Chemical Structure| 4511-42-6

A357015[ 4511-42-6 ]

(3S,6S)-3,6-Dimethyl-1,4-dioxane-2,5-dione

Reason: Optical isomers

Related Functional Groups of
[ 13076-17-0 ]

Esters

Chemical Structure| 7699-00-5

[ 7699-00-5 ]

(R)-Ethyl 2-hydroxypropanoate

Similarity: 0.89

Chemical Structure| 37555-99-0

[ 37555-99-0 ]

Diethyl 2-ethoxymalonate

Similarity: 0.87

Chemical Structure| 138-22-7

[ 138-22-7 ]

Butyl 2-hydroxypropanoate

Similarity: 0.83

Chemical Structure| 25383-99-7

[ 25383-99-7 ]

Sodium 2-((2-(stearoyloxy)propanoyl)oxy)propanoate

Similarity: 0.82

Chemical Structure| 4344-84-7

[ 4344-84-7 ]

5-Oxotetrahydrofuran-2-carboxylic acid

Similarity: 0.79

Related Parent Nucleus of
[ 13076-17-0 ]

Other Aliphatic Heterocycles

Chemical Structure| 1932281-42-9

[ 1932281-42-9 ]

(R)-1,4-Dioxane-2-carboxylic acid

Similarity: 0.83

Chemical Structure| 1821739-82-5

[ 1821739-82-5 ]

(S)-1,4-Dioxane-2-carboxylic acid

Similarity: 0.83

Chemical Structure| 60456-26-0

[ 60456-26-0 ]

(R)-Oxiran-2-ylmethyl butyrate

Similarity: 0.67

Chemical Structure| 51877-54-4

[ 51877-54-4 ]

Potassium oxirane-2-carboxylate

Similarity: 0.66

Chemical Structure| 13429-83-9

[ 13429-83-9 ]

(1S,4R)-4,7,7-Trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptane-1-carboxylic acid

Similarity: 0.64

; ;