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1990-29-0

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1990-29-0 Usage

Chemical Properties

white to off-white powder

Uses

D-Altrose is the epimer of D-glucose at C3 and have recently been discovered to possess antioxidant properties by the suppression of reactive oxygen species production in mitochondria due to competiti on with D-glucose at the cellular level.

Definition

An aldohexose that is isomeric with glucose, tallose, allose, and others.

Purification Methods

Crystallise D-altrose from aqueous EtOH. If it is obtained by the hydrolysis of the acetate, then it may contain sodium and acetate ions. Ions are best removed by dissolving in H2O, passing through suitable columns of ion-exchange resins, e.g. Amberlite IR-120 and Duolite A, and concentrating in a vacuum to a syrup. This is dissolved in MeOH, filtered and evaporated in a vacuum desiccator over granular CaCl2. The thick syrup is inoculated with seed crystals, stirred, and before it sets to a magma of crystals, transfer the crystals with MeOH to a Büchner funnel. Recrystallise them in the same way. -D-Altrofuranoside has initial [] D ~-69o (c 4, H2O) which mutarotates to +33o. [Richtmeyer Methods in Carbohydrate Chemistry I 107 Academic Press 1962, Beilstein 1 IV 4301, see Angyal Adv Carbohydrate Chem Biochem 42 15 1984 for ratio of anomers in solution.]

Check Digit Verification of cas no

The CAS Registry Mumber 1990-29-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,9 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1990-29:
(6*1)+(5*9)+(4*9)+(3*0)+(2*2)+(1*9)=100
100 % 10 = 0
So 1990-29-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4-,5+,6+/m1/s1

1990-29-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name D-altrose

1.2 Other means of identification

Product number -
Other names (2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexanal

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Processing Aids and Additives
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:1990-29-0 SDS

1990-29-0Relevant articles and documents

Isolation and structures of virescenosides from the marine-derived fungus Acremonium striatisporum

Afiyatullov, Shamil Sh.,Kalinovsky, Anatoly I.,Antonov, Alexandr S.,Zhuravleva, Olesya I.,Khudyakova, Yuliya V.,Aminin, Dmitry L.,Yurchenko, Anton N.,Pivkin, Mikhail V.

, p. 66 - 71 (2016)

Four new diterpene glycosides, virescenosides R1 (1), R2 (2), R3 (3) and Z (4) were isolated from a marine strain of Acremonium striatisporum KMM 4401 associated with the holothurian Eupentacta fraudatrix. Structures of 1-3 were determined as the corresponding biosides having isopimaradiene-type aglycons with additional oxidation and unsaturation patterns. Virescenosides Z (4) was structurally identified as altroside, containing 7-en-6-one group in the tricyclic aglycon moiety. The compounds 1-4 were examined for inhibition of non-specific esterase activity in mouse lymphocytes.

Anti-inflammatory active components of the roots of Datura metel

Qin, Ze,Zhang, Jin,Chen, Liang,Liu, Shu-Xiang,Zhao, Hai-Feng,Mao, Hui-Min,Zhang, Hong-Yang,Li, De-Fang

, p. 392 - 398 (2020/03/30)

One new phenolic glycoside, methyl 3,4-dihydroxyphenylacetate-4-O-[2-O-β-D-apisoyl-6-O-(2-hydroxybenzoyl)]-β-D-glucopyranoside (1), together with 10 known compounds (2–11), were isolated from the roots of Datura metel. The structures of these compounds we

Formation of Chiral Structures in Photoinitiated Formose Reaction

Stovbun,Skoblin,Zanin,Tverdislov,Taran,Parmon

, p. 108 - 116 (2018/04/05)

The possibility to synthesize biologically important sugars and other chiral compounds without any initiators in the UV-initiated reaction of formaldehyde in aqueous solution has been shown for the first time. An optically active condensed phase due to an

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