Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
HO2CCH(OH)CH(OH)CO2H
CAS Number:
Molecular Weight:
150.09
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352106
EC Number:
201-766-0
MDL number:
Beilstein/REAXYS Number:
1725147
Assay:
≥99.5%
Form:
granular, powder or crystals
Product Name
L-(+)-Tartaric acid, ≥99.5%
vapor density
5.18 (vs air)
Quality Level
assay
≥99.5%
form
granular, powder or crystals
optical activity
[α]20/D +13.5±0.5°, c = 10% in H2O
autoignition temp.
797 °F
mp
170-172 °C (lit.)
functional group
carboxylic acid, hydroxyl
SMILES string
O[C@H]([C@@H](O)C(O)=O)C(O)=O
InChI
1S/C4H6O6/c5-1(3(7)8)2(6)4(9)10/h1-2,5-6H,(H,7,8)(H,9,10)/t1-,2-/m1/s1
InChI key
FEWJPZIEWOKRBE-JCYAYHJZSA-N
General description
L-(+)-tartaric acid is an organic compound that is commonly used as a chiral auxiliary in reactions that involve the addition of a chiral nucleophile. It is also used as a resolving agent for the separation of enantiomers from a racemic mixture. Additionally, L-(+)-tartaric acid can also be used as a building block for the synthesis of other chiral compounds.
Application
L- (+)-Tartaric acid can be used as:
- A co-former for the synthesis of etravirine co-crystals.
- A mobile phase additive in thin-layer chromatography.
Still not finding the right product?
Explore all of our products under L-(+)-Tartaric acid
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
302.0 °F - closed cup
flash_point_c
150 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Andrea Bencini et al.
Chemical communications (Cambridge, England), 48(84), 10428-10430 (2012-09-18)
A chiral ditopic polyammonium receptor featuring two [9]aneN(3) moieties separated by a (S)-BINOL linker is able to selectively bind and sense in water (S,S)-tartaric acid over its (R,R)/meso forms.
Preparation of organotrifluoroborate salts: precipitation-driven equilibrium under non-etching conditions.
Alastair J J Lennox et al.
Angewandte Chemie (International ed. in English), 51(37), 9385-9388 (2012-08-21)
Yanfang Feng et al.
Bioresource technology, 125, 138-144 (2012-10-03)
The aim of this study was to develop a promising and competitive bioadsorbent with the abundant of source, low price and environmentally friendly characters to remove cationic dye from wastewater. The swede rape straw (Brassica napus L.) modified by tartaric
Global Trade Item Number
| SKU | GTIN |
|---|---|
| T109-12KG-A | 04061833644195 |
| T109-3KG-A | 04061837336492 |
| T109-500G-A | 04061837336508 |
