Select Region or Location
Americas
  • Argentina
  • Brazil
  • Canada
  • Mexico
  • United States
  • Other Americas
Europe
  • Austria
  • Belgium
  • Bulgaria
  • Croatia/Hrvatska
  • Cyprus
  • Czech Republic
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Liechtenstein
  • Lithuania
  • Luxembourg
  • Malta
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovak Republic
  • Slovenia
  • Spain
  • Sweden
  • Switzerland
  • Turkey
  • United Kingdom
  • Other Europe
Asia Pacific
  • Australia
  • China
  • India
  • Indonesia
  • Japan
  • Korea, Republic of
  • Malaysia
  • New Zealand
  • Philippines
  • Singapore
  • Thailand
  • Vietnam
  • Other Asia Pacific
Africa And Middle East
  • Egypt
  • Israel
  • Other Africa And Middle East
USD
Home Cart Sign in  
Chemical Structure| 15537-71-0 Chemical Structure| 15537-71-0
Chemical Structure| 15537-71-0

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

Ac-Penicillamine is a compound derived from the amino acid penicillamine, used for detoxification of heavy metals such as copper and mercury, and also for the treatment of Wilson's disease and rheumatoid arthritis.

Synonyms: N-Acetylpenicillamine

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

DE Stock

US Stock

Asia Stock

Global Stock

In Stock
{[ item.pr_size ]}{[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

  • {[ item.pr_size ]}
    {[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of Ac-D-Pen-OH

CAS No. :15537-71-0
Formula : C7H13NO3S
M.W : 191.25
SMILES Code : CC(C)(S)[C@H](C(O)=O)NC(C)=O
Synonyms :
N-Acetylpenicillamine
English Name :(S)-2-Acetamido-3-mercapto-3-methylbutanoic acid
MDL No. :MFCD00078887
InChI Key :MNNBCKASUFBXCO-YFKPBYRVSA-N
Pubchem ID :65532

Safety of Ac-D-Pen-OH

Application In Synthesis of Ac-D-Pen-OH

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 15537-71-0 ]

[ 15537-71-0 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 15537-71-0 ]
  • [ 67776-06-1 ]
  • [ 59-53-0 ]
  • [ 79032-48-7 ]
YieldReaction ConditionsOperation in experiment
With phosphate buffer; ethylenediaminetetraacetic acid for 0.0833333h;
  • 2
  • [ 15537-71-0 ]
  • [ 79032-48-7 ]
YieldReaction ConditionsOperation in experiment
72% With 3,3-dimethyl-2-nitroso-2,3-dihydrobenzo[d]isothiazole 1,1-dioxide; trifluoroacetic acid In acetonitrile at 20℃; for 0.5h; Sealed tube;
70% With hydrogenchloride; sulfuric acid; sodium nitrite In methanol; water for 0.25h;
67% With hydrogenchloride; sulfuric acid; sodium nitrite In methanol; water at 20℃; for 0.25h;
64% With hydrogenchloride; sulfuric acid; sodium nitrite In methanol; water at 20℃; for 0.5h; 1 Pulverized D-valine, N-acetyl-3-mercapto- (Fluka, 1.91 g, 10 mmol) was suspended in methanol (20 mL). IM HCl (20 mL) and sulfuric acid (2 niL) were added and the reaction mixture was cool to approximately room temperature. Sodium nitrite (1.38 g, 20 mmol) in water (20 mL) was added dropwisely over 5 minutes. D-valine, N-acetyl-3-mercapto- dissolved and formed a green solid. The suspension was stirred at room temperature for 25 minutes. The crystals were collected by filtration and washed with water, dried in vacuum to give the title compound (1.40 g, 64% yield). 1H NMR (300 MHz, CD3OD) δ 5.32 (s, 1 H), 2.04 (s, 3 H), 2.01 (s, 3 H), 1.97 (s, 3 H). . LRMS (APIMS) m/z 221 (MH+), 238 (MNH4+).
With PBS buffer; ethylenediaminetetraacetic acid; S-nitroso bovine serum albumin at 25℃; for 0.166667h;
With sulfuric acid; cis-nitrous acid Cooling with ice;
72 %Spectr. With 3,3-dimethyl-2-nitroso-2,3-dihydrobenzo[d]isothiazole 1,1-dioxide; trifluoroacetic acid In acetonitrile at 20℃; for 0.5h; Sealed tube; [B] General Procedure for Acid Catalyzed Nitrosation. General procedure: The threads of a 3 mL borosilicate scintillation vial were thoroughly taped with Teflon tape. To this vial containing a stir bar was added substrate (0.2 mmol, 1 equiv), and NO-1 (54.0 mg, 0.24 mmol, 1.2 equiv). Acetonitrile (2 mL) and trifluoracetic acid (3.1 pL, 20 mol %) was then added and the reaction was stirred at room temperature until completed (thin-layer chromatography). Upon completion, the solvent was removed under reduced pressure, crude mixture was directly absorbed onto silica and purified by silica gel chromatography to yield the desired product.
78 % With 3,3-dimethyl-2-nitroso-2,3-dihydrobenzo[d]isothiazole 1,1-dioxide In acetonitrile at 80℃;

  • 3
  • [ 59-53-0 ]
  • [ 79032-48-7 ]
  • [ 15537-71-0 ]
  • [ 67776-06-1 ]
YieldReaction ConditionsOperation in experiment
With phosphate buffer; ethylenediaminetetraacetic acid for 0.0833333h;
  • 4
  • [ 15537-71-0 ]
  • [ 2293-07-4 ]
  • ((1-acetamido-1-carboxy-2-methylpropan-2-yl)disulfaneyl)((4-methoxyphenyl)amino)methaniminium chloride [ No CAS ]
 

Historical Records

Technical Information

Categories