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CAS RN: 103-72-0 | ์ ํ๋ฒํธ: A5513
Phenyl Isothiocyanate [for HPLC Labeling]
์๋/๋ถ์ ๋ฐฉ๋ฒ: >99.0%(GC)
๋์์ด์:
- Isothiocyanic Acid Phenyl Ester
์ ํ๋ฌธ์:
| ํฌ์ฅ๋จ์ | ๊ฐ๊ฒฉ | ๋น์ผ์ถ๊ณ | 2-3์ผ ์ด๋ด ์ถ๊ณ | ์ถ๊ฐ๋ก ํ์ํ ๊ฒฝ์ฐ |
์ถํ ์ ๋ณด
|
|---|---|---|---|---|---|
| 5ML |
โฉ91,700
|
7 | ≥100 | ๋ฌธ์ |
โข๋ณธ ์ ํ์ ์ฌ๊ณ ๋ ์ผ๋ณธ ๋ณธ์ฌ์ ์ฌ๊ณ ์
๋๋ค. ์ฃผ๋ฌธ์, 5์ผ์์ ์คํ์ค๊น์ง ๋์ฐฉ๋ฉ๋๋ค.
โข๋ณธ๊ฑด์ ์๊ฐ๊ฒฉ์ ํ๊ตญ ๋๋ฆฌ์ ์ ์์ ํ๋งค๊ฐ๊ฒฉ์ ๋๋ค.์์ธํ ์ ๋ณด๊ฐ ํ์ํ์๋ฉด ์ฐ๋ฝํด ์ฃผ์ญ์์ค.( SEJIN CI Co., Ltd. (ํ๊ตญ์ด๋๋ฆฌ์ ) ์ ํ : 02-2655-2480 ์ด๋ฉ์ผ : sales@sejinci.co.kr)
โข๋ณด๊ด ์กฐ๊ฑด์ ์๊ณ ์์ด ๋ณ๊ฒฝ ๋ ์ ์์ต๋๋ค. ์ ํ ๋ณด๊ด ์กฐ๊ฑด์ ์ต์ ์๋ฃ๋ ํํ์ด์ง์ ๊ธฐ์ฌ๋์ด ์์ผ๋ ์ํด ๋ถํ๋๋ฆฝ๋๋ค.
โข๋ณธ๊ฑด์ ์๊ฐ๊ฒฉ์ ํ๊ตญ ๋๋ฆฌ์ ์ ์์ ํ๋งค๊ฐ๊ฒฉ์ ๋๋ค.์์ธํ ์ ๋ณด๊ฐ ํ์ํ์๋ฉด ์ฐ๋ฝํด ์ฃผ์ญ์์ค.( SEJIN CI Co., Ltd. (ํ๊ตญ์ด๋๋ฆฌ์ ) ์ ํ : 02-2655-2480 ์ด๋ฉ์ผ : sales@sejinci.co.kr)
โข๋ณด๊ด ์กฐ๊ฑด์ ์๊ณ ์์ด ๋ณ๊ฒฝ ๋ ์ ์์ต๋๋ค. ์ ํ ๋ณด๊ด ์กฐ๊ฑด์ ์ต์ ์๋ฃ๋ ํํ์ด์ง์ ๊ธฐ์ฌ๋์ด ์์ผ๋ ์ํด ๋ถํ๋๋ฆฝ๋๋ค.
| ์ ํ๋ฒํธ | A5513 |
Purity/Analysis Method
|
>99.0%(GC) |
| M.F. / M.W. | C__7H__5NS = 135.18 |
| ๋ฌผ๋ฆฌ์ ์ํ (20 โ) | Liquid |
๋ณด๊ด ์กฐ๊ฑด
|
Refrigerated (0-10ยฐC) |
| ๋ถํ์ฑ ๊ฐ์ค ํ์์ ๋ณด๊ด | Store under inert gas |
| ํผํด์ผ ํ ์กฐ๊ฑด | Moisture Sensitive,Heat Sensitive |
์ฉ๊ธฐ
|
5ML-Ampule (์ด๋ฏธ์ง ๋ณด๊ธฐ) |
| CAS RN | 103-72-0 |
| Reaxys-RN | 471392 |
| PubChem Substance ID | 87563160 |
| SDBS | 4809 |
| Merck Index (14) | 7297 |
| MDL ๋ฒํธ | MFCD00004798 |
๊ท๊ฒฉํ
| Appearance | Colorless to Light yellow clear liquid |
| Purity(GC) | min. 99.0 % |
| Effect test of HPLC derivatization | Effective as labeling agent for DL-Alanine. |
| NMR | confirm to structure |
๋ฌผ์ฑ์น(์ฐธ๊ณ ์น)
| mp | -21 ยฐC |
| bp | 71 ยฐC/1 mmHg |
| flp | 88 ยฐC |
| ๋น์ค | 1.14 |
| ๊ตด์ ๋ฅ | 1.65 |
| ์ฉํด์ฑ (์ฉํด) | Alcohol, Ether |
GHS
| ํฝํ ๊ทธ๋จ |
|
| ์ ํธ ์๋ | Danger |
| ์ํ๋ฌผ ๋ฐ ์ ํด ๋ฑ๋ก | 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. |
| ์ฃผ์ ์ฌํญ | 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, hot surfaces, sparks, open flames and other ignition sources. 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. 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 : Store in a well-ventilated place. P405 : Store locked up. |
๋ฒ๊ท ์ ๋ณด
| RTECS # | NX9275000 |
์ด์ก ์ ๋ณด
| UN ๋ฒํธ | UN2922 |
| ๋ฑ๊ธ | 8 / 6.1 |
| ํฌ์ฅ ๊ทธ๋ฃน | II |
| HS ๋ฒํธ* | 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.

- 9)C. Z. Zimmerman, E. Appella, J. J. Pisano, Anal. Biochem. 1976, 75, 77.

- 10)F. Trefz, O. J. Byrd, M. E. Blaskovics, W. Kochen, P. Lutz, Clin. Chem. Acta 1976, 73, 431.

- 11)F. G. Wing-Kin, E. Grushka, J. Chromatogr. 1977, 142, 299.

- 12)E. J. Kikta, E. Grushka, J. Chromatogr. 1977, 135, 367.

- 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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PubMed Literature
๋ฌธ์
์ ํ๊ธฐ์ฌ
์ ํ๋ฌธ์ (๋ถ์ ์ฐจํธ๋ฅผ ์ ๊ณตํ์ง ๋ชปํ ์๋ ์์ผ๋ ์ํด ๋ฐ๋๋๋ค.)
SDS
์ธ์ด๋ฅผ ์ ํํ์ญ์์ค.
์์ฒญํ SDS๋ฅผ ์ฌ์ฉํ ์ ์์ต๋๋ค.
๋ฒ๊ฑฐ๋กญ๊ฒ ํด๋๋ ค ์ฃ์กํ์ง๋ง ์ด ์์ ๋ณด๋ค ๋ฌธ์ ํด์ฃผ์ญ์์ค.
๊ท๊ฒฉํ
์ํ์ฑ์ ์๏ผ ๊ฐ์ข ์ฆ๋ช ์
๋กฏํธ ๋ฒํธ๋ฅผ ์
๋ ฅํ์ญ์์ค.
์๋ชป๋ ๋กํธ ๋ฒํธ๊ฐ ์
๋ ฅ๋์์ต๋๋ค.
์ํ ์ํ์ฑ์ ์
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๋ณธ ์ ํ์ ์ํ์ํ์ฑ์ ์๋ ํ์ฌ ์ค๋น๋์ด ์์ง ์์ต๋๋ค.
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๋กฏํธ ๋ฒํธ๋ฅผ ์
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์๋ชป๋ ๋กํธ ๋ฒํธ๊ฐ ์
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์ฃ์กํฉ๋๋ค๋ง ์ฐพ์ผ์๋ ๋ถ์์ฐจํธ๋ ์์ต๋๋ค.