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Published TCIMAIL newest issue No.198
Maximum quantity allowed is 999
Size | Unit Price | Belgium | Japan* |
---|---|---|---|
5G |
€65.00
|
11 | ≥100 |
25G |
€208.00
|
11 | ≥100 |
*Stock available in Belgium will be delivered in 1 to 3 days
*Stock available in Japan will be delivered in 1 to 2 weeks (excludes regulated items and dry ice shipments).
Product Number | D2919 |
Purity / Analysis Method | >95.0%(HPLC) |
Molecular Formula / Molecular Weight | C__1__0H__1__7ClN__4O__3 = 276.72 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Frozen (<0°C) |
Store Under Inert Gas | Store under inert gas |
Condition to Avoid | Hygroscopic,Heat Sensitive |
CAS RN | 3945-69-5 |
Reaxys Registry Number | 8026872 |
PubChem Substance ID | 87560457 |
MDL Number | MFCD03613550 |
Appearance | White to Almost white powder to crystal |
Purity(HPLC) | min. 95.0 area% |
Purity(with Total Nitrogen) | min. 98.0 %(calcd.on dried substance) |
Drying loss | max. 17.0 % |
Solubility (soluble in) | Methanol |
Pictogram |
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Signal Word | Danger |
Hazard Statements | H302 : Harmful if swallowed. H314 : Causes severe skin burns and eye damage. |
Precautionary Statements | P260 : Do not breathe dust. P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection/ hearing protection. P303 + P361 + P353 : IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water. P301 + P330 + P331 : IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. P304 + P340 + P310 : IF INHALED: Remove person to fresh air and keep comfortable for breathing. Immediately call a POISON CENTER/doctor. P305 + P351 + P338 + P310 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Immediately call a POISON CENTER/doctor. |
UN Number | UN3261 |
Class | 8 |
Packing Group | II |
HS Number | 2934999090 |
To a solution of 3-phenylpropionic Acid (1.80 g, 12.0 mmol) and 2-phenylethylamine (1.60 g, 13.2 mmol) in MeOH (120 mL) was added DMTMM (3.65 g, 13.2 mmol) and the mixture was stirred at room temperature for 1 hour. The solvent was removed under reduced pressure. Saturated aqueous sodium bicarbonate solution (100 mL) was added to the residue. After being stirred for 10 minutes, the mixture was extracted with diethyl ether (100 mL). The separated organic layer was washed with deionized water (50 mL), 1 mol/L hydrochloric acid (50 mL), deionized water (50 mL) and brine (100 mL), dried over magnesium sulfate and filtered. The solvent was removed under reduced pressure and the residue was purified by column chromatography (2:1 ethyl acetate / hexane on SiO2), giving white solid (2.54 g, 84%).
The reaction mixture was monitored by TLC (hexane : ethyl acetate = 1 : 1, Rf = 0.30) and GC.
1H NMR (400 MHz, CDCl3); δ 7.05–7.28 (m, 10H), 5.31 (br s, 1H), 3.46 (q, J = 6.8 Hz, 2H), 2.92 (t, J = 7.6 Hz, 2H), 2.71 (t, J = 6.8 Hz, 2H), 2.40 (t, J = 7.6 Hz, 2H).
13C NMR (101 MHz, CDCl3); δ 172.0, 140.8, 138.8, 128.7 (2C), 128.6, 128.5, 128.3, 126.4, 126.2, 40.5, 38.5, 35.6, 31.6.
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