S8313
Sinapinic acid
Use tested for MALDI-TOF Mass Spec.
Synonym(s):
Sinapic acid, 3,5-Dimethoxy-4-hydroxycinnamic acid, 4-Hydroxy-3,5-dimethoxy-cinnamic acid, Sinapinic acid
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About This Item
Empirical Formula (Hill Notation):
C11H12O5
CAS Number:
Molecular Weight:
224.21
EC Number:
208-487-3
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
2699118
mp
~202 °C
SMILES string
COc1cc(\C=C\C(O)=O)cc(OC)c1O
InChI
1S/C11H12O5/c1-15-8-5-7(3-4-10(12)13)6-9(16-2)11(8)14/h3-6,14H,1-2H3,(H,12,13)/b4-3+
InChI key
PCMORTLOPMLEFB-ONEGZZNKSA-N
Application
Matrix for protein MALDI-MS
Other Notes
Also available as part of MALDI calibration kits MS-CAL1 and MS-CAL3.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Monika Zochowska et al.
PloS one, 4(5), e5569-e5569 (2009-05-15)
Bleomycin (BLM) is an anticancer antibiotic used in many cancer regimens. Its utility is limited by systemic toxicity and dose-dependent pneumonitis able to progress to lung fibrosis. The latter can affect up to nearly 50% of the total patient population
Clifton K Fagerquist et al.
Journal of biomedicine & biotechnology, 2010, 123460-123460 (2011-02-19)
A method has been developed to identify the α-subunit of Shiga toxin 2 (α-Stx2) from Escherichia coli O157:H7 using matrix-assisted laser desorption/ionization time-of-flight-time-of-flight tandem mass spectrometry (MALDI-TOF-TOF-MS/MS) and top-down proteomics using web-based software developed in-house. Expression of Stx2 was induced
Hiroe Kikuzaki et al.
Journal of natural products, 71(5), 861-865 (2008-03-05)
Four new phenolic glycosides, (2-hydroxy-3-methoxy-5-allyl)phenyl beta- d-(6-O-E-sinapoyl)glucopyranoside (1), (1' R,5' R)-5-(5-carboxymethyl-2-oxocyclopentyl)-3 Z-pentenyl beta-D-(6-O-galloyl)glucopyranoside (2), (S)-alpha-terpinyl [alpha-L-(2-O-galloyl)arabinofuranosyl]-(1-->6)-beta-D-glucopyranoside (3), and (R)-alpha-terpinyl [alpha-L-(2-O-galloyl)arabinofuranosyl]-(1-->6)-beta-D-glucopyranoside (4), were isolated from the berries of Pimenta dioica together with eight known flavonoids. The structures of 1-4 were elucidated