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CAS RN: 103-72-0 | 產品號碼: A5513
Phenyl Isothiocyanate [for HPLC Labeling]
![Phenyl Isothiocyanate [for HPLC Labeling] No-Image](/medias/A5513.jpg?context=bWFzdGVyfHJvb3R8NDkzODZ8aW1hZ2UvanBlZ3xhR0ptTDJobU55ODRPVEU1TnpNNU56STNPVEF5TDBFMU5URXpMbXB3Wnd8MDQyZmE0OWM2YjhiZTJjZjhlZmE0YWQyZjViNmZiMTlhZGE4ZGJlMmNhMTUwZDE4MWUzZDcyNzg3MTc3NWNmOA)
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產品號碼 | A5513 |
純度/分析方法 | >99.0%(GC) |
分子式 / 分子量 | C__7H__5NS = 135.18 |
外觀與形狀(20°C) | Liquid |
儲存條件 | Refrigerated (0-10°C) |
儲存在惰性氣體下 | Store under inert gas |
應避免的情況 | Moisture Sensitive,Heat Sensitive |
包裝和容器 | 5ML-Ampule (閲覽圖片) |
CAS RN | 103-72-0 |
Reaxys-RN | 471392 |
PubChem Substance ID | 87563160 |
SDBS (AIST Spectral DB) | 4809 |
Merck Index(14) | 7297 |
MDL編號 | MFCD00004798 |
產品規格
Appearance | Colorless to Light yellow clear liquid |
Purity(GC) | min. 99.0 % |
Effect test of HPLC derivatization | Effective as labeling agent for DL-Alanine. |
性質
熔點 | -21 °C |
沸點 | 71 °C/1 mmHg |
flp | 88 °C |
比重 | 1.14 |
折射率 | 1.65 |
溶解性(可溶於) | Alcohol, Ether |
GHS
圖形表示 |
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信號詞 | Danger |
危險性說明 | H301 : Toxic if swallowed. H314 : Causes severe skin burns and eye damage. H410 : Very toxic to aquatic life with long lasting effects. H227 : Combustible liquid. |
防範說明 | P501 : Dispose of contents/ container to an approved waste disposal plant. P273 : Avoid release to the environment. P270 : Do not eat, drink or smoke when using this product. P210 : Keep away from heat/sparks/open flames/hot surfaces. No smoking. P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection. P370 + P378 : In case of fire: Use dry sand, dry chemical or alcohol-resistant foam to extinguish. P391 : Collect spillage. P303 + P361 + P353 : IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water/shower. P301 + P330 + P331 : IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. P363 : Wash contaminated clothing before reuse. P301 + P310 + P330 : IF SWALLOWED: Immediately call a POISON CENTER/doctor. Rinse mouth. 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. P403 + P235 : Store in a well-ventilated place. Keep cool. P405 : Store locked up. |
相關法規
RTECS # | NX9275000 |
運輸資料
UN編號 | UN2922 |
類別 | 8 / 6.1 |
包裝類別 | II |
HS編碼* | 2930.90-900 |
Application
HPLC Labeling Reagent for Amines
The compound 1 is an HPLC labeling reagent, which has an isothiocyano group, can easily react with an amino group to form the corresponding thiourea. The resultant thiourea can be also derivatized into a phenylthiohydantoin (PTH) derivative under acidic conditions. The PTH is stable enough to reach the detector without any decomposition under reversed phase HPLC. An excellent chromatogram can be obtained by measuring at 269 nm for UV detection.
Application examples:
[Amino acids, Peptides]
1.5 µmol of a sample is dissolved into 1 mL of 60% aqueous pyridine solution containing labeling reagent 1 (15 mg), and incubated at 40 °C for 1 h.After cooling to room temperature, the reaction mixture is diluted with 1 mL of water, and excess amount of 1 is removed by extraction (benzene 2 mL x 4 times). The aqueous layer is evaporated, and dried in desiccator. To the residue, 1.5 mL of mixed solution (3 N HCl and 60% AcOH, 1 : 1) is added to hydrolyzed at 40 °C for 30 min under a nitrogen atmosphere. After cooling to room temperature, the reaction mixture is diluted with 2 mL of water, and extracted with 2 mL of ethyl acetate, next 2 mL of benzene. The organic layers are combined to use it as an HPLC sample.
[Amino acids, Peptides]
1.5 µmol of a sample is dissolved into 1 mL of 60% aqueous pyridine solution containing labeling reagent 1 (15 mg), and incubated at 40 °C for 1 h.After cooling to room temperature, the reaction mixture is diluted with 1 mL of water, and excess amount of 1 is removed by extraction (benzene 2 mL x 4 times). The aqueous layer is evaporated, and dried in desiccator. To the residue, 1.5 mL of mixed solution (3 N HCl and 60% AcOH, 1 : 1) is added to hydrolyzed at 40 °C for 30 min under a nitrogen atmosphere. After cooling to room temperature, the reaction mixture is diluted with 2 mL of water, and extracted with 2 mL of ethyl acetate, next 2 mL of benzene. The organic layers are combined to use it as an HPLC sample.
TCI Products Pamphlet
HPLC Labeling Reagents ( PDF 10MB )
HPLC Labeling Reagents ( PDF 10MB )
References
- 1)P. Edman, G. Begg, Eur. J. Biochem. 1967, 1, 80.
- 2)V. M. Stepanov, Anal. Biochem. 1971, 43, 209.
- 3)G. Frank, W. Strubert, Chromatographia 1973, 6, 522.
- 4)A. P. Graffeo, Anal. Lett. 1973, 6, 505.
- 5)A. Hagg, K. Langern, Chromatographia 1974, 7, 659.
- 6)A. P. Graffeo, B. L. Karger, in Instrumentation in Amino Acid Sequence Analysis, ed. by R. N. Perham, Academic Press, London, New York, San Francisco, 1975, p.111.
- 7)Z. Deyl, J. Chromatogr. 1976, 127, 91.
- 8)M. R. Downing, K. G. Mann, Anal. Biochem. 1976, 74, 298.
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- 13)C. Z. Zimmerman, E. Appella, J. J. Pisano, Anal. Biochem. 1977, 77, 569.
- 14)W. T. Butler, J. E. Finch, E. J. Miller, J. Biol. Chem. 1977, 252, 639.
- 15)M. N. Margolies, A. Brauer, J. Chromatogr. 1978, 148, 429.
- 16)M. Abrahamsson, K. Gröningsson, S. Castensson, J. Chromatogr. 1978, 154, 313.
- 17)J. Elion, M. Downing, K. Mann, J. Chromatogr. 1978, 155, 436 .
- 18)A. S. Bhown, J. E. Mole, W. L. Holloway, C. Bernett, J. Chromatogr. 1978, 156, 35.
- 19)R. L. Heinrikson, S. C. Meredith, Anal. Biochem. 1984, 136, 65.
- 20)J. J. L'Italien, S. B. H. Kent, J. Chromatogr. 1984, 283, 149.
- 21)R. R. Granberg, LC, Liq. Chromatogr. HPLC Mag. 1984, 2, 776.
- 22)B. A. Bidlingmeyer, S. A. Cohen, T. L. Tarvin, J. Chromatogr. 1984, 336, 93.
- 23)D. L. Christie, R. M. Hill, K. Isakow, P. M. Barling, Anal. Biochem. 1986, 154, 92.
- 24)S. A. Cohen, B. A. Bidlingmeyer, T. L. Tarvin, Nature (London) 1986, 320, 769.
- 25)L. E. Lavi, J. S. Holcenberg, D. E. Cole, J. Jolivent, J. Chromatogr. 1986, 377, 155.
- 26)D. Lanneluc-Sanson, C. T. Phan, R. L. Granger, Anal. Biochem. 1986, 155, 322.
- 27)V. Semensi, M. Sugumaran, LC-GC 1986, 4, 1108.
- 28)A. Lilova, T. Kleinschmidt, P. Nedkov, G. Braunitzer, Biol. Chem. Hoppe-Seyler 1986, 367, 1055.
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