*Storage: {[sel_prStorage]}
*Shipping: {[sel_prShipping]}
The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
Synonyms: S-Nitroso-N-acetylpenicillamine;SNAP
4.5
*For Research Use Only! Not for Human Use. We Do Not Sell to Patients.
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, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]} {[ getRatePrice(item.pr_usd,item.pr_rate,1,item.pr_is_large_size_no_price, item.discount_usd) ]} {[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]} |
Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]} | {[ item.p_spot_brand_remark ]} 1-2 weeks {[ item.pr_usastock ]} In Stock Inquiry - | {[ item.p_spot_brand_remark ]} 1-2 weeks {[ item.pr_chinastock ]} {[ item.pr_remark ]} In Stock Inquiry - | Login - + |
Please Login or Create an Account to: See VIP prices and availability
Asia Stock: Ship in 3-5 business days
EU Stock: ship in 0-1 business day
Global Stock: ship in 7-10 days
US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days
{[ item.p_spot_brand_remark ]}
1-2weeks
Inquiry
Inquiry
{[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]}
{[ getRatePrice(item.pr_usd,1,item.mem_rate,item.pr_is_large_size_no_price, item.pr_usd) ]}
{[ item.p_spot_brand_remark ]}
1-2weeks
Inquiry
Inquiry
{[ getRatePrice(item.pr_usd,item.pr_rate,1,item.pr_is_large_size_no_price, item.vip_usd) ]}
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]}
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]}
In Stock
- +
Please Login or Create an Account to: See VIP prices and availability
Asia Stock: Ship in 3-5 business days
EU Stock: ship in 0-1 business day
Global Stock: ship in 7-10 days
US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
| CAS No. : | 79032-48-7 |
| Formula : | C7H12N2O4S |
| M.W : | 220.25 |
| SMILES Code : | CC(SN=O)(C)[C@@H](NC(C)=O)C(O)=O |
| Synonyms : |
S-Nitroso-N-acetylpenicillamine;SNAP
|
| English Name : | (S)-2-Acetamido-3-methyl-3-(nitrosothio)butanoic acid |
| MDL No. : | MFCD00153852 |
* 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.

| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| With phosphate buffer; ethylenediaminetetraacetic acid for 0.0833333h; |
| Yield | Reaction Conditions | Operation 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℃; |

| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| With phosphate buffer; ethylenediaminetetraacetic acid for 0.0833333h; |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| In water | 2 Hexopyranoside, 4,6-diamino-3-[(3-amino-3-deoxyhexopyranosyl)oxy]-2- hydroxycyclohexyl 2,6-diamino-2,3,6-trideoxy- (SAFC, 31.32 mg, 67.15 mmol) and the product of Example 1 (73.942 mg, 335.72 mmol) were mixed and dissolved in water (5 mL). The resultant solution was freeze dried to give 105 mg of the title compound. NMR (300 MHz, D2O) δ 5.67 (d, J= 3.9 Hz, 1 H), 5.03 (d, J= 3.9 Hz, 1 H), 4.89 (s, 3.75 H), 4.18 (s, 1.25 H), 3.93-3.31 (m, 16 H), 3.18 (dd, J= 7.2 & 13.8 Hz, 1 H), 2.46 (m, 1 H), 2.21 (m 1 H), 2.13-1.71 (m, 2 H), 1.97 (s, 3.4 H), 1.91 (S, 23 H), 1.88 (s, 11.7 H), 1.33 (s, 3.4 H), 1.29 (s, 3.4 H). |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| In not given (Ar); mixing iron complex with nitroso compd.; not isolated, detected by ESR; |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| With 3-(N-morpholino)propanesulfonic acid; ethylenediaminetetraacetic acid; L-Cysteine; potassium chloride; sodium sulfite at 22℃; Electrochemical reaction; |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| With Cu2O In aq. phosphate buffer at 25℃; |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| With hydrogenchloride; sulfuric acid; sodium nitrite | Synthesis of S-Nitroso-N-acetyl-D-penicillamine (SNAP) Equimolar ratios of N-acetylpenicillamine (NAP) and sodium nitrite were added to a reaction vessel, which had 1:1 mixture of water and methanol containing 2 M HCl and 2 M H2SO4, and stirred for 30 minutes. The reaction vessel was cooled in an ice bath to precipitate the SNAP crystals. After precipitation of SNAP crystals, they were collected by filtration and washed with water to remove unreacted salts, and air dried. |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| Synthesis of S-Nitroso-N-acetyl-D-penicillamine (SNAP) 2 wt % SNAP was dissolved in 80% ethanol and 3 ml of the resulting solution was added into the completely dispersed chitosan and the mixing process was continued to obtain complete encapsulation of SNAP. |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| With ethylenediaminetetraacetic acid In aq. buffer at 37℃; Darkness; |