What is the L-(+)-THREOSE?

L-(+)-THREOSE is syrup, while it's Molecular Formula is C4H8O4. syrup L-Threose is a significant degredation product of ascorbic acid, with high potential to glycate and crosslink lens proteins in vitro forming a stable lens tissue.

What is the CAS number for L-(+)-THREOSE?

The CAS number of L-(+)-THREOSE is 95-44-3.

What is L-(+)-THREOSE (95-44-3) used for?

L-(+)-THREOSE, also known as the L-stereoisomer of threose, is a significant degradation product of ascorbic acid. It is a colorless to light yellow viscous liquid with high potential to glycate and crosslink lens proteins in vitro, forming a stable lens tissue. As a major in vivo degradation product of ascorbate, L-(+)-THREOSE plays a crucial role in various applications across different industries.InChI:InChI=1/C4H8O4/c5-2-1-8-4(7)3(2)6/h2-7H,1H2/t2?,3?,4-/m0/s1

What is the L-(+)-THREOSE?

L-(+)-THREOSE is syrup, while it's Molecular Formula is C4H8O4. syrup L-Threose is a significant degredation product of ascorbic acid, with high potential to glycate and crosslink lens proteins in vitro forming a stable lens tissue.

What is the CAS number for L-(+)-THREOSE?

The CAS number of L-(+)-THREOSE is 95-44-3.

What is L-(+)-THREOSE (95-44-3) used for?

L-(+)-THREOSE, also known as the L-stereoisomer of threose, is a significant degradation product of ascorbic acid. It is a colorless to light yellow viscous liquid with high potential to glycate and crosslink lens proteins in vitro, forming a stable lens tissue. As a major in vivo degradation product of ascorbate, L-(+)-THREOSE plays a crucial role in various applications across different industries.InChI:InChI=1/C4H8O4/c5-2-1-8-4(7)3(2)6/h2-7H,1H2/t2?,3?,4-/m0/s1

Product classification

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95-44-3

Product Name:L-(+)-THREOSE
Molecular Formula:C₄H₈O₄
Molecular Weight:120.105
Appearance:syrup

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Product Details

pd_meltingpoint:162-163℃

Appearance:syrup

Purity:99%

Factory supply L-(+)-THREOSE 95-44-3 with low price

Molecular Formula:C4H8O4
Molecular Weight:120.105
Appearance/Colour:syrup
Vapor Pressure:0.000223mmHg at 25°C
Melting Point:162-163℃
Refractive Index:1.619
Boiling Point:290.6 °C at 760mmHg
PKA:12.49±0.20(Predicted)
Flash Point:129.5 °C
PSA：69.92000
Density:1.698 g/cm³
LogP:-1.94320

L-(+)-THREOSE(Cas 95-44-3) Usage

Definition

ChEBI: The L-stereoisomer of threose; a major in vivo degradation product of ascorbate.

InChI:InChI=1/C4H8O4/c5-2-1-8-4(7)3(2)6/h2-7H,1H2/t2?,3?,4-/m0/s1

95-44-3 Relevant articles

-

Hockett et al.

, p. 278 (1938)

Selective Reductive Dimerization of CO2into Glycolaldehyde

Zhang, Dan,Jarava-Barrera, Carlos,Bontemps, Sébastien

, p. 4568 - 4575 (2021/05/04)

The selective dimerization of CO2 into g...

Shape-selective Valorization of Biomass-derived Glycolaldehyde using Tin-containing Zeolites

Tolborg, S?ren,Meier, Sebastian,Saravanamurugan, Shunmugavel,Fristrup, Peter,Taarning, Esben,Sádaba, Irantzu

, p. 3054 - 3061 (2016/11/17)

A highly selective self-condensation of ...

Catalytic effect of aluminium chloride on the example of the conversion of sugar model compounds

Schwiderski, Martin,Kruse, Andrea

, p. 64 - 70 (2015/04/14)

Abstract In this work, the catalytic eff...

Asymmetric organocatalytic formation of protected and unprotected tetroses under potentially prebiotic conditions

Burroughs, Laurence,Clarke, Paul A.,Forintos, Henrietta,Gilks, James A. R.,Hayes, Christopher J.,Vale, Matthew E.,Wade, William,Zbytniewski, Myriam

experimental part, p. 1565 - 1570 (2012/04/05)

Esters of proteinogenic amino acids effi...

95-44-3 Process route

: 96-26-4,26776-70-5
dihydroxyacetone

: 141-46-8
Glycolaldehyde

: 470-14-4
DL-dendroketose

: 95-43-2,95-44-3,533-49-3,583-50-6,1758-51-6,7558-94-3,29825-68-1,29884-64-8,38982-45-5
DL-threose

: 95-43-2,95-44-3,533-49-3,583-50-6,1758-51-6,7558-94-3,29825-68-1,29884-64-8,38982-45-5
DL-glycero-tetrulose

: 41247-05-6
(+/-)-xylose

: 488-84-6,527-50-4,551-84-8,2042-27-5,5556-48-9,5962-29-8,7558-89-6,25577-44-0,83946-43-4
DL-erythro-[2]pentulose

: 488-84-6,527-50-4,551-84-8,2042-27-5,5556-48-9,5962-29-8,7558-89-6,25577-44-0,83946-43-4
DL-threo-[2]pentulose

Conditions

Conditions	Yield
Amberlite IRA-400 (HO-); In water; for 0.25h; Product distribution; Ambient temperature; further catalysts;	0.7 mg 0.6 mg 0.8 mg 0.3 mg 8.0 mg 1.0 mg

: 96-26-4,26776-70-5
dihydroxyacetone

: 141-46-8
Glycolaldehyde

: 470-14-4
DL-dendroketose

: 95-43-2,95-44-3,533-49-3,583-50-6,1758-51-6,7558-94-3,29825-68-1,29884-64-8,38982-45-5
DL-threose

: 95-43-2,95-44-3,533-49-3,583-50-6,1758-51-6,7558-94-3,29825-68-1,29884-64-8,38982-45-5
DL-glycero-tetrulose

: 41247-05-6
(+/-)-xylose

: 488-84-6,527-50-4,551-84-8,2042-27-5,5556-48-9,5962-29-8,7558-89-6,25577-44-0,83946-43-4
DL-erythro-[2]pentulose

: 488-84-6,527-50-4,551-84-8,2042-27-5,5556-48-9,5962-29-8,7558-89-6,25577-44-0,83946-43-4
DL-threo-[2]pentulose

Conditions

Conditions	Yield
Amberlite IRA-400 (HO-); In water; for 0.25h; Product distribution; Ambient temperature; further catalysts;	0.7 mg 0.6 mg 0.8 mg 0.3 mg 8.0 mg 1.0 mg

95-44-3 Upstream products

34693-27-1
(3aR,6S,6aR)-6-hydroxy-tetrahydro-2,2-dimethylfuro[2,3-d][1,3]dioxole
50-81-7
ascorbic acid
141-46-8
Glycolaldehyde
96-26-4
dihydroxyacetone

95-44-3 Downstream products

87-79-6
L-sorbose
2319-57-5
threitol
3154-37-8
3,4-dihydroxy-2-phenylhydrazono-butyraldehyde phenylhydrazone
781577-54-6
calcium(II) oxalate

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