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ChemicalBook >> CAS DataBase List >>9-Fluorenylmethyl chloroformate

9-Fluorenylmethyl chloroformate

CAS No.
28920-43-6
Chemical Name:
9-Fluorenylmethyl chloroformate
Synonyms
FMOC-CL;FoMc-Cl;(9H-fluoren-9-yl)Methyl carbonochloridate;FMOC-C;fmoc-ci;9-FLUORENYLMETHOXYCARBONYL CHLORIDE;FMOC-CHLORIDE;9-Fluorenylmethyl;FMOC-C1;Fluorenylmethyloxycarbonyl chloride
CBNumber:
CB7234569
Molecular Formula:
C15H11ClO2
Molecular Weight:
258.7
MDL Number:
MFCD00001138
MOL File:
28920-43-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-06-04 16:00:12
Product description Number Pack Size Price
(9-Fluorenylmethyl) chloroformate Novabiochem? 8.52259 25g $59.6
(9-Fluorenylmethyl) chloroformate for synthesis 8.18203 500mg $37.4
(9-Fluorenylmethyl) chloroformate Novabiochem? 8.52259 100g $168
(9-Fluorenylmethyl) chloroformate for synthesis 8.18203 5G $127
(9-Fluorenylmethyl) chloroformate for synthesis 8.18203 25g $327
More product size

9-Fluorenylmethyl chloroformate Properties

Melting point 62-64 °C(lit.)
Boiling point 365.79°C (rough estimate)
Density 1.1780 (rough estimate)
refractive index 1.5330 (estimate)
storage temp. 2-8°C
solubility dioxane: 0.1 g/mL, clear, colorless
form Crystalline Powder
color White to very pale yellow
Sensitive Moisture Sensitive
BRN 2279177
Stability Hygroscopic, Moisture Sensitive
InChI InChI=1S/C15H11ClO2/c16-15(17)18-9-14-12-7-3-1-5-10(12)11-6-2-4-8-13(11)14/h1-8,14H,9H2
InChIKey IRXSLJNXXZKURP-UHFFFAOYSA-N
SMILES C(Cl)(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O
LogP 3.45
CAS DataBase Reference 28920-43-6(CAS DataBase Reference)
FDA UNII 9PLB0BTT90
UNSPSC Code 12352108
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)
GHS05
Signal word  Danger
Hazard statements  H314
Precautionary statements  P260-P280-P301+P330+P331-P303+P361+P353-P304+P340+P310-P305+P351+P338
PPE Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  C,T
Risk Statements  34-20/21/22
Safety Statements  26-36/37/39-45-27
RIDADR  UN 3261 8/PG 2
WGK Germany  3
RTECS  LQ6250000
10-21
TSCA  No
HazardClass  6.1
PackingGroup  II
HS Code  29159020
Storage Class 8A - Combustible corrosive hazardous materials
Hazard Classifications Eye Dam. 1
Skin Corr. 1B
REACH Registrations Active
Limited Quantities 1 Kg (2.2 lbs) (solid)
Excepted Quantities Max Inner Pack (30g or 30ml) and Max Outer Pack (500g or 500ml)
NFPA 704
1
3 1

9-Fluorenylmethyl chloroformate price More Price(131)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 8.52259 (9-Fluorenylmethyl) chloroformate Novabiochem? 28920-43-6 25g $59.6 2026-04-30 Buy
Sigma-Aldrich 8.18203 (9-Fluorenylmethyl) chloroformate for synthesis 28920-43-6 500mg $37.4 2026-04-30 Buy
Sigma-Aldrich 8.52259 (9-Fluorenylmethyl) chloroformate Novabiochem? 28920-43-6 100g $168 2026-04-30 Buy
Sigma-Aldrich 8.18203 (9-Fluorenylmethyl) chloroformate for synthesis 28920-43-6 5G $127 2026-04-30 Buy
Sigma-Aldrich 8.18203 (9-Fluorenylmethyl) chloroformate for synthesis 28920-43-6 25g $327 2026-04-30 Buy
Product number Packaging Price Buy
8.52259 25g $59.6 Buy
8.18203 500mg $37.4 Buy
8.52259 100g $168 Buy
8.18203 5G $127 Buy
8.18203 25g $327 Buy

9-Fluorenylmethyl chloroformate Chemical Properties,Uses,Production

Description

9-Fluorenylmethyl chloroformate (Fmoc-C1) is a significant biochemical reagent introduced by Carpino. It has been widely utilized as a reagent for the introduction of the 9-fluorenylmethoxycarbonyl (Fmoc moiety) in both peptide and nucleotide synthesis, as well as serving as a coupling agent in peptide synthesis[1]. Furthermore, Fmoc-C1 can function as a versatile fluorescent labeling reagent for primary and secondary amines[2].

Chemical Properties

9-Fluorenyl chloroformate appears as white crystals with a melting point of 62–64 °C. It is soluble in organic solvents such as CH?Cl?, THF, and dioxane. It reacts with alcohols, ammonia or amines, and water.

Uses

9-Fluorenylmethyl chloroformate can be used as N-protecting reagent for oligonucleotide and peptide syntheses. It can act as reagent for the introduction of Fmoc-amino-protecting group, which is stable towards acids but is readily cleaved under mildly basic non-hydrolytic conditions.

Uses

9-Fluorenylmethyl chloroformate is an N-Protecting agent for peptides research and was used for the pre-column derivatization of the biogenic amines (BAs) cadaverine (Cad), histamine (Him), octopami ne (Ocp), phenylethylamine (Pea), putrescine (Put), spermidine (Spd), spermine (Spm), tyramine (Tym).

General Description

Fmoc chloride is a derivatizing agent.

Flammability and Explosibility

Not classified

Safety Profile

A poison. Mutation data reported. A corrosive. When heated to decomposition it emits toxic vapors of Cl-.

Purification Methods

If the IR contains no OH bands (at ~3000 cm-1) due to the hydrolysis product 9-fluorenylmethanol, then purify it by recrystallisation from dry Et2O. IR (CHCl3) has a band at 1770 cm-1 (C=O), and the NMR (CDCl3) has  at 4-4.6 (m 2H, CHCH2) and 7.1-7.8 (m, 8 aromatic H) ppm. The azide (FMOC-N3) has m 89-90o (from -1hexane) and IR (CHCl3) at 2135 (N3) and 1730 (C=O) cm , and the carbazate (FMOC-NHNH2) has m 171o(dec) (from nitromethane), IR (KBr) 3310, 3202 (NH) and 1686 (CONH) cm-1. [Caprino & Han J Org Chem 37, 3404 1972 , J Am Chem Soc 92 5748 1970, Koole et al. J Org Chem 59 1657 1989, Fürst et al. J Chromatogr 499 537 1990.]

References

[1] S. TANTRY; V. V B; G Vasanthakumar. Synthesis of peptides employing 9-fluorenylmethyl chloroformate as a coupling agent[J]. Letters in peptide science: LIPS, 2006, 10 1: 51-55. DOI:10.1007/BF02443642.
[2] H. A. MOYE  A. B. A Versatile Fluorogenic Labelling Reagent for Primary and Secondary Amines: 9-Fluorenylmethyl Chloroformate[J]. Analytical Letters, 1979, 12 1: 25-35. DOI:10.1080/00032717908082516.

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Related articles

Related Qustion

Ask a question
Q:What are the structural characteristics of 9-Fluorenylmethyl chloroformate?Anonymous - Aug 19,2025
A:The 9-Fluorenylmethyl chloroformate(FMOC-CL) molecule consists of a fluorenyl group and a chloroformate group. The fluorenyl group is an aromatic ring structure with unique optical properties, while the chloroformate group is a reactive acyl chloride group that reacts with amines, alcohols, and other compounds.
Q:What is 9-Fluorenylmethyl chloroformate?Anonymous - Aug 19,2025
A:9-Fluorenylmethyl chloroformate, also known as FMOC-CL, is a highly versatile reagent with varied applications in organic synthesis. It is most frequently used to introduce the base-labile Fmoc-protecting group to amine functionalities, particularly during the production of Fmoc-protected amino acids.

View Lastest Price from 9-Fluorenylmethyl chloroformate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
 FMOC-CL pictures 2026-07-21 FMOC-CL
28920-43-6
$750.00 1kg 99 50tons Xinxiang Juyuan Biological Technology Co., Ltd.
	9-Fluorenylmethyl chloroformate pictures 2026-07-09 9-Fluorenylmethyl chloroformate
28920-43-6
$1.00-8.00 1KG 99% Henan Fengda Chemical Co., Ltd
9-Fluorenylmethyl chloroformate pictures 2026-06-30 9-Fluorenylmethyl chloroformate
28920-43-6
1KG 98 10000KGS Shaanxi Dideu New Materials Co. Ltd
  •  FMOC-CL pictures
  • FMOC-CL
    28920-43-6
  • $750.00
  • 99
  • Xinxiang Juyuan Biological Technology Co., Ltd.
CHLOROFORMIC ACID 9-FLUORENYLMETHYL ESTER EMOCCI 9-FLUORENYLMETHYL CHLOROFORMATE (FMOC CL) Fmoc-Cl(9-FluorenylmethoxycarbonylChloride) Fmoc-Clsee22072 FMOC-CL CHLOROFORMIC ACID 9-FLUORENYLMETHYL ESTER 9-Fluorenylmethoxycarbonyl chloride (Fmoc-Cl) FMOC-CL, 9-FLLUORENYLMETHYL CHLOROFOMATE Fmco-chloride(9-Fluorenyl methyl chloroformate) Chloroformic acid 9H-fluoren-9-ylmethyl ester 9-Fluorenylmethyl Chloroformate [N-Protecting Agent for Peptides Research] 9-Fluorenylmethylchloroformate,98% 9-FLUOROMETHANOL ( FMOC ) 9-FLUOROMETHANOL ( FMOC-ONSU ) FMOC-CL (9-FLUORENYLMETHYL CHLOROFORMATE) 9-Fluorenylmethylchloroformate (Fmoc-chloride) 9-Fluorenylmethoxycarbonyl chloride, 9-Fluorenylmethyl chloroformate, Fmoc-Cl AminoTag FMoc chloride 97% FMOC chloride [FMOC-CL] 9-FluorenylMethyl ChloroforMate, 97+% Fmoc chloride, >=98% 9 - fluorene chlorine Methyl forMate Fmoc-Chloride≥ 98% (HPLC) (9-Fluorenylmethyl) chloroformate Novabiochem (9-Fluorenylmethyl) chloroformate for synthesis chloro-formicacifluoren-9-ylmethylester Formicacid,chloro-,fluoren-9-ylmethylester N-9-FLUORENYLMETHYL CHLOROFORMATE RARECHEM FM OC 0001 9-FLUOROENYLMETHYL CHLOROFORMATE 9-FLUORENEMETHYL CHLOROFORMATE 9-FLUORENMETHYL CHLOROFORMATE 9-FLUORENYLMETHYL CHLOROFORMATE 9-(Chloroformyloxymethyl)-9H-fluorene Chloridocarbonic acid (9H-fluoren-9-yl)methyl ester Chlorocarbonic acid (9H-fluoren-9-ylmethyl) ester Chloroformic acid (9H-fluoren-9-yl)methyl CARBONOCHLORIDIC ACID, 9H-FLUOREN-9-YLMETHYL ESTER 9-Fluoroe Fmoc chloride,9-Fluorenylmethoxycarbonyl chloride, 9-Fluorenylmethyl chloroformate, Fmoc-Cl Chloroformic acid 9- (9H-Fluoren-9-yl)methyl carbonochloridoate 9-FluorenylMethyl chloroforMate, 98% 1GR 9-FluorenylMethyl chloroforMate, 98% 5GR Fmoc-Cl Chloroformic Acid 9-Fluorenylmethyl Ester (9H-Fluoren-9-ylmethoxy)carbonyl Chloride 9H-fluoren-9-ylMethylester carbonochloridric acid (9-FLUORENYLMETHYL) CHLOROFORMATE FOR SY FMoc-Cl)FMoc chl (9H-Fluoren-9-yl)methyl carbonochloridoate, FMOC-chloride (9H-Fluoren-9-yl)MethOxy]Carbonyl Cl Chloroformic acid 9-fluorenylmethyl ester(Fmoc-CL) 9-Fluorenylmethyl chloroformate, Chloroformic acid 9-fluorenylmethyl este, Fmoc-Cl uorenyL Fmoc-Cl(99%) Fluorenylmethyl Research 9-FluorenylmethylChloroformate[N-ProtectingAgentforPeptidesResearch]> Fmoc-CL Chloroformic acid 9-fluorenylmethyl ester,98%
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