D-(+)-Trehalose dihydrate
Code | Size | Price |
---|
CDX-T0202-G025 | 25 g | £108.00 |
Quantity:
CDX-T0202-G100 | 100 g | £304.00 |
Quantity:
CDX-T0202-G500 | 500 g | £804.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Storage:
Short Term: +20°C. Long Term: +4°C
Images
Documents
Further Information
Alternate Names/Synonyms:
alpha,alpha-Trehalose; alpha-D-Glucopyranosyl-alpha-D-glucopyranoside; Trehalose dihydrate
Appearance:
White powder.
CAS:
6138-23-4
EClass:
32160000
Form (Short):
liquid
Handling Advice:
Keep cool and dry.Protect from light and moisture.
InChi:
InChI=1S/C12H22O11.2H2O/c13-1-3-5(15)7(17)9(19)11(21-3)23-12-10(20)8(18)6(16)4(2-14)22-12;;/h3-20H,1-2H2;2*1H2/t3-,4-,5-,6-,7+,8+,9-,10-,11-,12-;;/m1./s1
InChiKey:
DPVHGFAJLZWDOC-PVXXTIHASA-N
Long Description:
Chemical. CAS: 6138-23-4. Formula: C12H22O11 . 2H2O. MW: 378.33. Synthetic. Natural alpha-linked disaccharide formed by alpha-glucose units. Can be synthesized by bacteria, fungi, plants and invertebrate animals. It is implicated in anhydrobiosis, the ability of plants and animals to withstand prolonged periods of desiccation/dehydration. The sugar is thought to form a gel phase as cells dehydrate, which prevents disruption of internal cell organelles. Rehydration then allows normal cellular activity to be resumed without the major, lethal damage that would normally follow a dehydration/rehydration cycle. It has high water retention capabilities, and is used in food and cosmetics. Used as a cryoprotectant in a variety of cell freezing media, in solid dosage formulations, most notably in quick-dissolving tablets and to preserve foods, enzymes, vaccines, cells in a dehydrated state at room temperature. Major carbohydrate energy storage molecule used by insects for flight. Osmolyte, a chemical chaperone and inducer of autophagy, that has been reported to protect cells against numerous environmental stresses. This compound contains many properties that allow it to stabilize partially unfolded protein molecules and inhibit protein aggregation.
MDL:
MFCD00071594
Molecular Formula:
C12H22O11 . 2H2O
Molecular Weight:
378.33
Package Type:
Vial
Product Description:
Natural alpha-linked disaccharide formed by alpha-glucose units. Can be synthesized by bacteria, fungi, plants and invertebrate animals. It is implicated in anhydrobiosis, the ability of plants and animals to withstand prolonged periods of desiccation/dehydration. The sugar is thought to form a gel phase as cells dehydrate, which prevents disruption of internal cell organelles. Rehydration then allows normal cellular activity to be resumed without the major, lethal damage that would normally follow a dehydration/rehydration cycle. It has high water retention capabilities, and is used in food and cosmetics. Used as a cryoprotectant in a variety of cell freezing media, in solid dosage formulations, most notably in quick-dissolving tablets and to preserve foods, enzymes, vaccines, cells in a dehydrated state at room temperature. Major carbohydrate energy storage molecule used by insects for flight. Osmolyte, a chemical chaperone and inducer of autophagy, that has been reported to protect cells against numerous environmental stresses. This compound contains many properties that allow it to stabilize partially unfolded protein molecules and inhibit protein aggregation.
Purity:
>99%
SMILES:
OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@@H](O[C@@H]2[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O2)O1.O.O
Solubility Chemicals:
Soluble in water (50mg/ml).
Transportation:
Non-hazardous
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at +4°C.
References
(1) J.H. Crowe; Adv. Exp. Med. Biol. 594, 143 (2007) | (2) N.K. Jain & I. Roy; Protein Sci. 18, 24 (2009) | (3) G. Iturriaga, et al.; Int. J. Mol. Sci. 10, 3793 (2009) | (4) S. Ohtake & Y.J. Wang; J. Pharm. Sci. 100, 2020 (2011) | (5) P.L. Chiu, et al.; Micron. 42, 762 (2011) | (6) E. Emanuele; Curr. Drug Targets. 15, 551 (2014) | (7) P. Mardones, et al.; Sci. Signal. 9, 416 (2016)
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